U.S. patent application number 17/181953 was filed with the patent office on 2021-07-08 for compositions for treatment or prevention of infectious inflammatory diseases, or compositions for immune enhancement, comprising, tryptophanyl-trna synthetase as an active ingredient.
The applicant listed for this patent is MirimGENE CO. LTD.. Invention is credited to Young Ha AHN, Mi Rim JIN, Sunghoon KIM.
Application Number | 20210205423 17/181953 |
Document ID | / |
Family ID | 1000005462143 |
Filed Date | 2021-07-08 |
United States Patent
Application |
20210205423 |
Kind Code |
A1 |
KIM; Sunghoon ; et
al. |
July 8, 2021 |
Compositions for Treatment or Prevention of Infectious Inflammatory
Diseases, or Compositions for Immune Enhancement, Comprising,
Tryptophanyl-tRNA Synthetase as an Active Ingredient
Abstract
The present invention relates to a composition for treatment or
prevention of infectious inflammatory diseases comprising
tryptophanyl-tRNA synthetase as an active ingredient, and a
composition for immune enhancement. More specifically, the present
invention relates to a pharmaceutical composition for treatment or
prevention of infectious inflammatory diseases comprising
tryptophanyl-tRNA synthetase as an active ingredient, a food
composition for preventing or improving, a veterinary composition
for preventing or treating, and a composition for immune
enhancement comprising a tryptophanyl-tRNA synthetase as an active
ingredient, respectively. The composition of the present invention
can be effectively used for preventing or treating diseases of
humans and animals caused by infection from bacteria, viruses or
fungi and the like by inhibiting infections such as bacterial,
viral, and fungal infections at an early stage particularly through
activating innate immune response.
Inventors: |
KIM; Sunghoon; (Seoul,
KR) ; JIN; Mi Rim; (Seoul, KR) ; AHN; Young
Ha; (Daejeon, KR) |
|
Applicant: |
Name |
City |
State |
Country |
Type |
MirimGENE CO. LTD. |
Incheon |
|
KR |
|
|
Family ID: |
1000005462143 |
Appl. No.: |
17/181953 |
Filed: |
February 22, 2021 |
Related U.S. Patent Documents
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Application
Number |
Filing Date |
Patent Number |
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15686557 |
Aug 25, 2017 |
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17181953 |
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PCT/KR2016/001944 |
Feb 26, 2016 |
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15686557 |
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Current U.S.
Class: |
1/1 |
Current CPC
Class: |
C12Y 601/01002 20130101;
A61P 31/10 20180101; A61K 38/53 20130101; A61P 31/04 20180101; A23L
33/10 20160801; A23V 2002/00 20130101; A23L 33/40 20160801; C12N
9/00 20130101; A61P 31/12 20180101; A61P 29/00 20180101; A61P 31/00
20180101 |
International
Class: |
A61K 38/53 20060101
A61K038/53; C12N 9/00 20060101 C12N009/00; A61P 29/00 20060101
A61P029/00; A61P 31/04 20060101 A61P031/04; A61P 31/00 20060101
A61P031/00; A61P 31/10 20060101 A61P031/10; A61P 31/12 20060101
A61P031/12; A23L 33/10 20060101 A23L033/10; A23L 33/00 20060101
A23L033/00 |
Foreign Application Data
Date |
Code |
Application Number |
Feb 26, 2015 |
KR |
10-2015-0027617 |
Claims
1.-12. (canceled)
13. A composition for preventing or treating an infectious
inflammatory disease in a subject caused by a virus, a bacterium,
or fungus comprising tryptophanyl-tRNA synthetase as an active
ingredient, wherein the tryptophanyl-tRNA synthetase is selected
from the group consisting of SEQ ID NO:1, SEQ ID NO:2, SEQ ID NO:3,
SEQ ID NO:4, SEQ ID NO:5, SEQ ID NO:6, SEQ ID NO:7, and SEQ ID NO:8
and wherein the tryptophanyl-tRNA synthetase induces neutrophil
accumulation in the body of the subject.
14. The composition of claim 13, wherein the composition is a
pharmaceutical composition or a veterinary composition.
15. The composition of claim 13, wherein the composition is a food
composition.
16. The composition of claim 13, wherein the infectious
inflammatory disease is selected from the group consisting of
salmonellosis, food poisoning, typhoid, paratyphoid, sepsis, septic
shock, systemic inflammatory response syndrome (SIRS), multiple
organ dysfunction syndrome (MODS), pneumonia, pulmonary
tuberculosis, tuberculosis, cold, influenza, airway infection,
rhinitis, nasopharyngitis, otitis media, bronchitis, lymphadenitis,
mumps, adenolymphitis, cheilitis, stomatitis, arthritis, myositis,
dermatitis, vasculitis, gingivitis, pericementitis, keratitis,
conjunctivitis, wound infection, peritonitis, hepatitis,
osteomyelitis, cellulitis, meningitis, encephalitis, brain abscess,
encephalomyelitis, cerebral meningitis, osteomyelitis, nephritis,
carditis, endocarditis, enteritis, gastritis, esophagitis,
duodenitis, colitis, urinary tract infection, cystitis, vaginitis,
cervicitis, salpingitis, infectious erythema, bacterial dysentery,
abscess and ulcer, bacteremia, diarrhea, dysentery, gastritis,
gastroenteritis, genitourinary abscess, open wound or wound
infection, purulent inflammation, abscesses, boils, pyoderma,
impetigo, folliculitis, cellulitis, wound infection after surgery,
scalded skin syndrome, skin burn syndrome, thrombotic
thrombocytopenia, hemolytic uremic syndrome, renal failure,
pyelonephritis, glomerulonephritis, nervous system abscess, otitis
media, sinusitis, pharyngitis, tonsillitis, mastoiditis, soft
tissue inflammation, dental infection, dacryocystitis, pleurisy,
abdominal abscess, liver abscess, cholecystitis, spleen abscess,
pericarditis, myocarditis, placentitis, amniotic fluid infection,
mammitis, mastitis, puerperal fever, toxic shock syndrome, lyme
disease, gas gangrene, atherosclerosis, Mycobacterium avium
syndrome (MAC), enterohaemorrhagic Escherichia coli (EHEC)
infection, enteropathogenic Escherichia coli (EPEC) infection,
enteroinvasive Escherichia coli (EIEC) infection,
methicillin-resistant Staphylococcus aureus (MRSA) infections,
vancomycin-resistant Staphylococcus aureus (VRSA) infections and
listerosis.
17. A composition for immune enhancement comprising tryptophanyl
tRNA synthetase as an active ingredient, wherein the
tryptophanyl-tRNA synthetase is selected from the group consisting
of SEQ ID NO:1, SEQ ID NO:2, SEQ ID NO:3, SEQ ID NO:4, SEQ ID NO:5,
SEQ ID NO:6, SEQ ID NO:7, and SEQ ID NO:8.
Description
CROSS-REFERENCE TO RELATED APPLICATIONS
[0001] The present application is divisional application of U.S.
application Ser. No. 15/686,557, filed on Aug. 25, 2017, which is a
continuation-in-part of International Application No.:
PCT/KR2016/001944, filed on Feb. 26, 2016, which claims priority to
Korean Application No.: 10-2015-0027617, filed on Feb. 26, 2015,
which are incorporated by reference in their entirety.
SEQUENCE LISTING
[0002] The instant application contains a Sequence Listing which
has been submitted electronically in ASCII format and is hereby
incorporated by reference in its entirety. Said ASCII copy, created
on Nov. 7, 2017, is named 10524-006146-US0_SL.txt and is 36,342
bytes in size.
TECHNICAL FIELD
[0003] The present invention relates to a composition for treatment
or prevention of infectious inflammatory diseases, or composition
for immune enhancement, comprising tryptophanyl-tRNA synthetase
(TrpRS) as an active ingredient, more particularly, the present
invention relates to a pharmaceutical composition for treatment or
prevention of infectious inflammatory diseases containing
tryptophanyl-tRNA synthetase as an active ingredient, a food
composition for prevention or improvement, a veterinary composition
for treatment or prevention, and a composition for immune
enhancement comprising tryptophanyl-tRNA synthetase as an active
ingredient, more particularly, the present invention relates to a
method for preventing, improving or treating infectious
inflammatory diseases or a method for immune enhancement comprising
administering an effective amount of a tryptophanyl-tRNA synthetase
as an active ingredient to a subject in need thereof, and to a use
for producing a therapeutic agent for preventing, improving or
treating infectious inflammatory diseases or an agent for immune
enhancement.
BACKGROUND TECHNOLOGY
[0004] Aminoacyl-tRNA synthetase (AARS) is an enzyme that mediates
amino acid-specific binding to tRNA, and it plays a pivotal role in
protein production. Recently, it is known that these AARSs are
involved in various life phenomena such as apoptosis, angiogenesis,
and inflammation reaction in addition to its intrinsic functions.
Tryptophanyl-tRNA synthetase (TrpRS) belongings to class I of AARS
and is present in the cytoplasm of a cell. It is known that
mini-TrpRS, which does not contain extra N-terminal domain of
TrpRS, is an angiostatic factor which is activated by IFN-.gamma..
It is observed that full-length TrpRS was secreted in vascular
cells, but it is not yet known what role it plays in the body (Guo
M et al. (2013), Nat. Chem. Biol, 9 (3): 145-153).
DETAILED DESCRIPTION OF THE INVENTION
Technical Problem
[0005] While searching the novel biological functions of
tryptophanyl-tRNA synthetase (TrpRS) in addition to its essential
functions related with protein synthesis, the present inventors
found that tryptophanyl-tRNA synthetase (TrpRS) activates innate
immune responses and inhibits the infection of bacteria, fungi,
viruses and the like, completing the present invention.
[0006] Accordingly, an aspect of the present invention is to
provide a pharmaceutical composition for treating or preventing
infectious inflammatory diseases comprising tryptophanyl-tRNA
synthetase as an active ingredient.
[0007] Another aspect of the present invention is to provide a food
composition for treating or preventing infectious inflammatory
diseases comprising tryptophanyl-tRNA synthetase as an active
ingredient.
[0008] It is still another aspect of the present invention to
provide a veterinary composition for treating or preventing
infectious inflammatory diseases comprising tryptophanyl-tRNA
synthetase as an active ingredient.
[0009] Another aspect of the present invention is to provide a
composition for immune enhancement comprising a tryptophanyl-tRNA
synthetase as an active ingredient.
[0010] Another aspect of the present invention is to provide a
method for preventing, ameliorating or treating infectious
inflammatory diseases comprising administering to a subject in need
thereof an effective amount of tryptophanyl-tRNA synthetase as an
active ingredient.
[0011] Still another aspect of the present invention is to provide
a use for the preparation of an agent for preventing, ameliorating
or treating infectious inflammatory diseases comprising as a
tryptophanyl-tRNA synthetase an active ingredient.
[0012] Still another aspect of the present invention is to provide
a method for immune enhancement comprising administering to a
subject in need thereof an effective amount of tryptophanyl-tRNA
synthetase as an active ingredient.
[0013] Still another aspect of the present invention is to provide
a use for producing an agent for immune enhancement comprising a
tryptophanyl-tRNA synthetase as an active ingredient.
Technical Solution
[0014] An embodiment of the present invention is to provide a
pharmaceutical composition for treating or preventing infectious
inflammatory diseases comprising tryptophanyl-tRNA synthetase as an
active ingredient.
[0015] Another embodiment of the present invention is to provide a
food composition for preventing or ameliorating infectious
inflammatory diseases comprising tryptophanyl-tRNA synthetase as an
active ingredient.
[0016] Another embodiment of the present invention is to provide a
veterinary composition for the prophylaxis or treatment of
infectious inflammatory diseases comprising tryptophanyl-tRNA
synthetase as an active ingredient.
[0017] Another embodiment of present invention is to provide a
composition for immune enhancement comprising tryptophanyl tRNA
synthetase as an active ingredient.
[0018] Another embodiment of present invention is to provide a
method for preventing, ameliorating or treating infectious
inflammatory diseases comprising administering to a subject in need
thereof an effective amount of tryptophanyl-tRNA synthetase as an
active ingredient.
[0019] Another embodiment of present invention is to provide a use
for preparing an agent for preventing, ameliorating or treating
infectious inflammatory diseases comprising tryptophanyl-tRNA
synthetase as an active ingredient.
[0020] Another embodiment of present invention is to provide a
method for immune enhancement comprising administering to a subject
in need thereof an effective amount of tryptophanyl-tRNA synthetase
as an active ingredient.
[0021] Another embodiment of present invention is to provide a use
for preparing an agent for immune enhancement containing
tryptophanyl-tRNA synthetase as an active ingredient.
[0022] Hereinafter, the present invention will be described in
detail.
[0023] The present invention provides a pharmaceutical composition
for treating or preventing infectious inflammatory diseases
comprising tryptophanyl-tRNA synthetase as an active
ingredient.
[0024] The tryptophanyl-tRNA synthetase may be represented by any
one of the amino acid sequences selected from the group consisting
of SEQ ID NO: 1 to SEQ ID NO: 8.
[0025] The inventors first discovered and disclosed herein that
TrpRS has the function of inhibiting infections such as bacterial,
viral and fungal infections by activating the immune system,
particularly innate immune responses.
[0026] Specifically, one following Example shows that TrpRS was
secreted outside the cells from the beginning of infection, when
peripheral blood mononuclear cells are infected with bacteria and
viruses, and secreted TrpRS increases the production of
TNF-.alpha., an inflammatory cytokine. Another Example shows that
when peripheral blood mononuclear cells are infected with bacteria,
TrpRS is actively secreted rather than secretion due to pyroptosis,
and TrpRS, which is already present in the cell, is secreted
without induction of its gene expression.
[0027] Another Example shows that TrpRS increased the secretion of
various cytokines, particularly in monocytes and macrophages, and
promotes macrophage differentiation and activation of their
phagocystic function.
[0028] In still another Example, it is shown that the action of
TrpRS increased the cell fluidity of neutrophils and monocytes, and
when TrpRS is injected into the body, it induces intraperitoneal
neutrophil concentration, increases the number of neutrophils and
macrophages, and promote their activation.
[0029] Still another Example shows that the secretion of
TNF-.alpha. and MIP-1.alpha. was decreased and the mortality rate
was increased when a TrpRS-specific antibody was treated with a
bacterial-infected cell to inhibit the activity of TrpRS.
[0030] Further, in another Example, when TrpRS was administered to
a living body, the number of neutrophils in the abdominal cavity
was increased, and it was confirmed that the bacteria were removed
from the liver and spleen. This confirms that TrpRS promotes the
action of removing the infecting bacteria from the body and
remarkably reduces the mortality rate associated with
infection.
[0031] Therefore, the present inventors discovered and disclosed
herein that the tryptophan tRNA synthetase (TrpRS) of the present
invention is secreted to the outside of the cell by infections such
as bacterial, viral and fungal infection and TrpRS activates immune
cells and is effective in the treatment or prevention of infectious
inflammatory diseases.
[0032] As used herein, TrpRS or TrpRS polypeptide" refers to a
polypeptide known as tryptophanyl-tRNA synthetase (TrpRS or WRS).
The TrpRS polypeptide may be a polypeptide having any one of the
amino acid sequences selected from the group consisting of SEQ ID
NO: 1 to SEQ ID NO: 8. The TrpRS of the present invention also
includes functional equivalents thereof. "Polypeptide" is used
interchangeably with "polypeptides" or "protein(s)" and refers to a
polymer of amino acid residues, as is commonly found in natural
state proteins.
[0033] The above mentioned functional equivalent means a sequence
homology (i.e., identity) of at least 70% or more, preferably 80%
or more, and more preferably 90% or more with any one of amino acid
sequences selected from the group consisting of SEQ ID NO: 1 to SEQ
ID NO: 8. For example, a polypeptide having 70%, 71%, 72%, 73%,
74%, 75%, 76%, 77%, 78%, 79%, 80%, 81%, 82%, 83%, 84%, 85%, 86%,
87%, 88%, 89%, 90%, 91%, 92%, 93%, 94%, 95%, 96%, 97%, 98%, 99%, or
100% of a sequence homology, which has a substantially homogenous
physiological activity as a polypeptide represented by any one of
amino acid sequences selected from the group consisting of SEQ ID
NO: 1 to SEQ ID NO: 8. Herein, the "substantially homogenous
physiological activity" means the activation of immune cell
functions such as cytokine production and secretion, cell fluidity
and phagocytosis of macrophage, induction of neutrophil
concentration in the body, and enhancement of the action of
removing the infecting bacteria.
[0034] The functional equivalents may result from the addition,
substitution or deletion of an amino acid in any part of any one of
the amino acid sequences selected from the group consisting of SEQ
ID NO: 1 to SEQ ID NO: 8. The substitution of the amino acid is
preferably a conservative substitution. Examples of conservative
substitutions of amino acids present in nature are as follows:
aliphatic amino acids (Gly, Ala, Pro), hydrophobic amino acids
(Ile, Leu, Val), aromatic amino acids (Phe, Tyr, Trp), acidic amino
acids (Asp, Glu), basic amino acids (His, Lys, Arg, Gln, Asn) and
sulfur-containing amino acids (Cys, Met). Also the functional
equivalents include variants in which some of the amino acids are
deleted in the amino acid sequence of the TrpRS polypeptide of the
present invention. The deletion or substitution of the amino acid
is preferably located in a region that is not directly related to
the physiological activity of the polypeptide of the present
invention. The deletion of the amino acid is also preferably
located at a site that is not directly involved in the
physiological activity of the TrpRS polypeptide. Also variants in
which several amino acids have been added at both ends or sequences
of the amino acid sequence of the TrpRS polypeptide are included.
Also polypeptide derivatives in which some of the chemical
structures of the polypeptides are modified while maintaining the
basic skeleton of the polypeptide according to the present
invention and its physiological activity are included within the
scope of functional equivalents of the present invention. This
includes, for example, structural modifications to alter the
stability, shelf stability, volatility, or solubility of the
polypeptides of the present invention.
[0035] In the present specification, sequence homology and
homogeneity are defined as the percentage of amino acid residues in
the candidate sequence to the amino acid sequence of TrpRS after
aligning the candidate sequence with the amino acid sequence of
TrpRS (any one of the amino acid sequences selected from the group
consisting of SEQ ID NO: 1 to SEQ ID NO: 8), and introducing gaps.
If necessary, conservative substitutions as a part of sequence
homology are not considered to obtain maximum percent sequence
homology. In addition, the stretch, deletion, or insertion of
N-terminus, C-terminus, or internal region in the amino acid
sequence of TrpRS is not interpreted as a sequence that affects
sequence homology or homology. In addition, such homology can be
determined by standard methods used to compare similar portions of
amino acid sequences of two polypeptides. BLAST or similar computer
program aligns two polypeptides so that each amino acid is
optimally matched (along the full length sequence of one or two
sequences or along the predicted portion of one or two sequences).
The program provides a PAM 250 (Standard Scoring Matrix; Dayhoff et
al., in Atlas of Protein Sequence and Structure, vol 5, supp 3,
1978), which provides a default opening penalty and default gap
penalty and can be used in conjunction with a computer program. For
example, percentage homogeneity can be calculated by multiplying
the total number of identical matches by 100 and then dividing by
the sum of the number of gaps introduced into the longer sequence
to align two sequences with the length of the longer sequence in
the matched span.
[0036] Polypeptides according to the present invention can be
extracted naturally or constructed by genetic engineering methods.
The nucleic acid can be constructed by PCR amplification using
appropriate primers. Alternatively, DNA sequences may be
synthesized by standard methods known in the art, for example,
using an automated DNA synthesizer (commercially available from
Biosearch or Applied Biosystems). The constructed nucleic acid is
inserted into a vector comprising one or more expression control
sequences (e.g., promoters, enhancers, etc.) operatively linked to
the expression of the nucleic acid, and a host cell is transformed
with the recombinant expression vector formed therefrom. The
resulting transformant is cultured under the conditions suitable
for expression of the nucleic acid, and the substantially pure
polypeptide expressed by the nucleic acid is recovered from the
culture. The recovery can be carried out using methods known in the
art (for example, chromatography). As used herein, "substantially
pure polypeptide" means that the polypeptide according to the
invention is substantially free of any other proteins derived from
the host cell. Genetic engineering methods for the synthesis of
polypeptides of the present invention can be found in the following
references: Maniatis et al., Molecular Cloning; A laboratory
Manual, Cold Spring Harbor laboratory, 1982; Sambrook et al.,
Molecular Cloning: A Laboratory Manual, Cold Spring Harbor Press,
N.Y., Second (1998) and Third (2000) Editions; Gene Expression
Technology, Method in Enzymology, Genetics and Molecular Biology,
Method in Enzymology, Guthrie & Fink (eds.), Academic Press,
San Diego, Calif., 1991; R. A. Hitzeman et al., J. Biol. Chem.,
255:12073-12080, 1990.
[0037] In addition, the polypeptides of the present invention can
be readily prepared by chemical synthesis known in the art
(Creighton, Proteins, Structures and Molecular Principles, W. H.
Freeman and Co., NY, 1983). Representative methods include, but are
not limited to, liquid or solid phase synthesis, fractional
condensation, F-MOC or T-BOC chemistry (Chemical Approaches to the
Synthesis of Peptides and Proteins, Williams et al., Eds., CRC
Press, Boca Raton Fla., 1997; A Practical Approach, Athert on &
Sheppard, Eds., IRL Press, Oxford, England, 1989).
[0038] The tryptophanyl-tRNA synthetase of the composition
according to the present invention can be used in its own form or
in the form of a salt, preferably a pharmaceutically acceptable
salt. As used herein, the term "pharmaceutically acceptable" means
physiologically acceptable and does not usually cause an allergic
reaction or the like when administered to humans and the salt is
preferably an acid addition salt formed by a pharmaceutically
acceptable free acid. As the free acid, an organic acid and an
inorganic acid can be used. The organic acids include, but are not
limited to, citric, acetic, lactic, tartaric, maleic, fumaric,
formic, propionic, oxalic, trifluoroacetic, benzoic, gluconic,
methosulfonic, glycolic, succinic, Glutamic acid and aspartic acid.
The inorganic acid includes, but is not limited to, hydrochloric
acid, bromic acid, sulfuric acid, and phosphoric acid.
[0039] "Pharmacologically acceptable" refers to a nontoxic
composition that is physiologically acceptable and does not inhibit
the action of the active ingredient when administered to humans and
does not normally cause an allergic reaction such as
gastrointestinal disorder, dizziness, or the like. The
pharmaceutical composition of the present invention can be
formulated into various forms according to the route of
administration by a method known in the art together with a
pharmaceutically acceptable carrier for the immuno-stimulatory
effect of tryptophanyl-tRNA synthetase. Such carriers include all
kinds of solvents, dispersion media, oil-in-water or water-in-oil
emulsions, aqueous compositions, liposomes, microbeads and
microsomes.
[0040] The route of administration may be oral or parenteral.
Parenteral administration methods include, but are not limited to,
intravenous, intramuscular, intraarterial, intramedullary,
intrathecal, intracardiac, transdermal, subcutaneous,
intraperitoneal, intranasal, enteral, topical, sublingual or rectal
administration can be.
[0041] When the pharmaceutical composition of the present invention
is orally administered, the pharmaceutical composition of the
present invention may be formulated into a powder, a granule, a
tablet, a pill, a sugar tablet, a capsule, a liquid, a gel, a
syrup, a suspension, a wafer, and the like. Examples of suitable
carriers include saccharides including lactose, dextrose, sucrose,
sorbitol, mannitol, xylitol, erythritol and maltitol, and starches
including corn starch, wheat starch, rice starch and potato starch,
and cellulose including methyl cellulose, sodium carboxymethyl
cellulose and hydroxypropylmethyl cellulose, and fillers such as
gelatin, polyvinyl pyrrolidone and the like. In addition,
cross-linked polyvinylpyrrolidone, agar, alginic acid or sodium
alginate may optionally be added as a disintegrant. Further, the
pharmaceutical composition may further comprise an anti-coagulant,
a lubricant, a wetting agent, a flavoring agent, an emulsifying
agent and an antiseptic agent.
[0042] In addition, when administered parenterally, the
pharmaceutical composition of the present invention may be
formulated according to methods known in the art in the form of
injections, transdermal drugs, and nasal inhalers together with a
suitable parenteral carrier. In the case of the injections, they
must be sterilized and protected from contamination of
microorganisms such as bacteria and fungi. Examples of suitable
carriers for injections include, but are not limited to, solvents
or dispersion media containing water, ethanol, polyols (e.g.,
glycerol, propylene glycol and liquid polyethylene glycol, etc.),
mixtures thereof and/or vegetable oils can be. More preferably,
suitable carriers include, but are not limited to, Hank's solution,
Ringer's solution, phosphate buffered saline (PBS) containing
triethanolamine, or isotonic solutions such as sterile water for
injection, 10% ethanol, 40% propylene glycol and 5% dextrose can be
used. In order to protect the injection from microbial
contamination, various antibacterial and antifungal agents such as
parabens, chlorobutanol, phenol, sorbic acid, thimerosal and the
like may be further included. In addition, the injections may in
most cases also contain isotonic agents such as sugars or sodium
chloride.
[0043] Examples of transdermal dosage forms include ointments,
creams, lotions, gels, solutions for external use, pastes,
liniments, and air rolls. The "transdermal administration" means
that a pharmaceutical composition is locally administered to the
skin, whereby an effective amount of the active ingredient
contained in the pharmaceutical composition is delivered into the
skin. For example, the pharmaceutical composition of the present
invention may be prepared into a spray-type formulation, which is
gently pricked with a 30-gauge thin injection needle or directly
applied to the skin. These formulations are described in the
literature (Remington's Pharmaceutical Science, 15th Edition, 1975,
Mack Publishing Company, Easton, Pa.), which is a prescription
commonly known in pharmaceutical chemistry.
[0044] In the case of inhalation dosage forms, the compounds used
according to the present invention may be formulated into a
pressurized pack or a pressurized pack using a suitable propellant,
for example dichlorofluoromethane, trichlorofluoromethane,
dichlorotetrafluoroethane, carbon dioxide or other suitable gases.
It can be conveniently delivered in the form of an aerosol spray
from a nebulizer. In the case of a pressurized aerosol, the dosage
unit may be determined by providing a valve that delivers a metered
amount. For example, gelatin capsules and cartridges for use in an
inhaler or insufflator may be formulated to contain a compound and
a powder mix of a suitable powder base such as lactose or
starch.
[0045] As other pharmaceutically acceptable carriers, reference may
be made to those described in the following references (Remington's
Pharmaceutical Sciences, 19th ed., Mack Publishing Company, Easton,
Pa., 1995).
[0046] The pharmaceutical composition according to the present
invention may also contain one or more buffers (e.g., saline or
PBS), a carbohydrate (e.g., glucose, mannose, sucrose or dextran),
an antioxidant, a bacteriostat, a chelating agent (e.g., EDTA or
glutathione), an adjuvant (e.g., Aluminum hydroxide), a suspending
agent, a thickening agent, and/or a preservative.
[0047] In addition, the pharmaceutical composition of the present
invention may be formulated using methods known in the art so as to
provide rapid, sustained or delayed release of the active
ingredient after administration to the mammal.
[0048] In addition, the pharmaceutical composition of the present
invention may be administered in combination with a known compound
having an effect of preventing or treating an immune disease or an
infectious inflammatory disease.
[0049] In the inflammatory diseases caused by the bacterial
infection of the present invention, the bacterium may preferably be
selected one or more from the group consisting of Acinetobacter
baumannii, Acinetobacter calcoaceticus, Acinetobacter haemolyticus,
Acinetobacter hydrophila, Actinobacillus actinomycetemcomitans,
Aeromonas hydrophila, Alcaligenes xylosoxidans, Bacteroides
distasonis, Bacteroides fragilis, Bacteroides melaninogenicus,
Bacteroides ovatus, Bacteroides thetaiotaomicron, Bacteroides
vulgatus, Bartonella henselae, Bordetella pertussis, Branhamella
catarrhalis, Brucella melitensis, Brucella abortus, Brucella canis,
Burkholderia cepacia, Burkholderia mallei, Burkholderia
pseudomallei, Campylobacter coli, Campylobacter fetus,
Campylobacter jejuni, Citrobacter diversus, Citrobacter freundi,
Citrobacter koseri, Coxiella burnetii, Edwarsiella tarda, Ehrlichia
chafeenis, Eikenella corrondens, Enterobacter aerogenes,
Enterobacter agglomerans, Enterobacter cloacae, Escherichia coli,
Escherichia fergusonii, Escherichia vulneris, Flavobacterium
meningosepticum, Francisella tularensis, Fusobacterium spp.,
Haemophilus ducreyi, Haemophilus influenzae, Haemophilus
parainfluenzae, Helicobacter pylori, Kingella kingae, Klebsiella
oxytoca, Klebsiella ozaenae, Klebsiella pneumoniae, Klebsiella
rhinoscleromatis, Legionella pneumophila, Listeria monocytogenes,
Listeria ivanovii, Moraxella catarrhalis, Morganella morganii,
Neisseria gonorrhoeae, Neisseria meningitides, Pasteurella
multoclda, Plesiomonas shigelloides, Porphyromonas asaccharolytica,
Porphyromonas gingivalis, Prevotella bivia, Prevotella buccae,
Prevotella corporis, Prevotella endodontalis, Prevotella
intermedia, Prevotella melaninogenica, Prevotella oralis, Proteus
mirabilis, Proteus myxofaclens, Proteus penner, Proteus vulgaris,
Providencia alcalifaciens, Providencia rettgeri, ProvidenCla
stuarfii, Pseudomonas aeruginosa, Pseudomonas fluorescens,
Ricketsia prowozekii, Salmonella bongori, Salmonella enterica,
Serratia marcescens, Shigella boydii, Shigella dysenteriae,
Shigella flexneri, Shigella sonnei, Staphylococcus aureus,
Staphylococcus epidermidis, Staphylococcus saprophyticus,
Stenotrophomonas maltophilia, Streptobacillus moniliformis, Vibrio
alginolyticus, Vibrio cholerae, Vibrio parahaemolyticus, Vibrio
vulunificus, Yersinia enterocolitica, Yersinia pestis, Yersinia
pseudotuberculosis, Mycobacterium tuberculosis complex,
Mycobacterium leprae and Mycobacterium lepromatosis, Mycobacterium
avium complex (MAC), Mycobacterium kansasii, and Mycobacterium
abscessus.
[0050] As used herein, the inflammatory diseases caused by
bacterial infections include bacterial infections occurring in
mammals and birds, and diseases accompanied by bacterial
infections, Preferably, it may be pneumonia, otitis media,
sinusitis, bronchitis, tonsillitis and mastoiditis associated with
infection by Streptococcus pneumoniae, Haemophilus influenzae,
Moraxella catarrhalis, Staphylococcus aureus or genus
Peptostreptococcus; Pharyngitis, rheumatic fever and
glomerulonephritis caused by infection by Streptococcus pyogenes,
Group C and G streptococcus, Clostridium diptheriae or
Actinobacillus haemolyticum; airway infections associated with
infection by Mycoplasma pneumoniae, Legionella pneumophila,
Streptococcus pneumoniae, Haemophilus influenzae, or Chlamydia
pneumoniae; Non-complex skin and soft-tissue infections, boils,
osteomyelitis and puerperal fever associated with infection by
Staphylococcus aureus, coagulase-positive Staphylococcus (e.g., S.
epidermidis, S. hemolyticus, etc.), Streptococcus pyogenes,
Streptococcus agalactiae, Streptococcus group C-F (micro-colony
Streptococcus), Viridans streptococcus, Corynebacterium
minutissimum, genus Clostridium, or Bartonella henselae;
Uncomplexed acute urinary tract infection; urethritis and
cervicitis associated with infection by Staphylococcus
saprophyticus or genus Enterococcus; and sexually transmitted
disease associated with infection by Chlamydia trachomatis,
Haemophilus ducreyi, Treponema pallidum, Ureaplasma urealyticum, or
Neiserria gonorrheae; toxic diseases associated with infection by
S. aureus (food poisoning and toxic shock syndrome), groups A, B
and C streptococci; ulcers associated with infection by
Helicobacter pylori; systemic fever syndrome associated with
infection by Borrelia recurrentis; lyme disease associated with
infection by Borrelia burgdorferi; conjunctivitis, keratitis and
dacryocystitis associated with infection by Chlamydia trachomatis,
Neisseria gonorrhoeae, S. aureus, S. pneumoniae, S. pyogenes, H.
influenzae or genus Listeria; Diffuse Mycobacterium avium syndrome
(MAC) disease associated with infection by Mycobacterium avium,
Mycobacterium intracellulare; Gastroenteritis associated with
infection by Campylobacter jejuni; Dental infection associated with
infection by viridans streptococcus; Persistent cough associated
with infection by Bordetella pertussis; Gas gangrene associated
with infection by Clostridium perfringens or the genus Bacteroides;
and atherosclerosis accompanied by infection by Helicobacter pylori
or Chlamydia pneumoniae. Bacterial infections that can be treated,
prevented or ameliorated by the composition of the present
invention and diseases caused by these infections are cited in J.
P. Sanford et al. ("The Sanford Guide To Antimicrobial Therapy",
26th, Antimicrobial Therapy, Inc., 1996).
[0051] The inflammatory disease caused by the bacterial infection
of the present invention is most preferably a disease caused by a
bacterial infection of Escherichia genus, Listeria genus,
Salmonella genus, or Staphylococcus genus.
[0052] The infectious inflammatory diseases caused by viruses
according to the present invention may include an inflammatory
disease caused by infection such as, for example, adenovirus,
herpes viruses (e.g., HSV-I, HSV-II, CMV or VZV), poxviruses (e.g.,
variola), orthopoxviruses such as vaccinia or Molluscum
contagiosum, picornavirus (e.g., Linovirus or enterovirus),
orthomycovirus (e.g., Influenza virus), paramyxovirus (e.g.,
5-para-influenza virus, mumps virus), measles virus and respiratory
syncytial virus (RSV), coronavirus (e.g., SARS), papovaviruses
(e.g., papilloma viruses that cause genital warts, common warts or
plantar warts), hepadnavirus (e.g. hepatitis B virus), flavivirus
(e.g., hepatitis B virus or hepatitis C virus or Denguevirus), or
retroviruses (e.g., lentiviruses such as HIV)), cytomegalovirus,
and the like. Preferably, it may be an inflammatory disease caused
by infection of the virus selected from the group consisting of
rhinovirus, coronavirus, influenza virus, respiratory syncytial
virus (RSV), adenovirus, parainfluenza virus, herpes simplex virus,
cytomegalovirus, and the like, which are caused by infection of
pneumonia, influenza (influenza), or viruses known to cause
respiratory tract infection.
[0053] The infectious inflammatory diseases caused by fungus
according to the present invention include disorders which are
related to the presence of fungus in a subject. For instance, the
infectious inflammatory diseases may include topical, mucosal
and/or systemic fungal infections caused by, for example, Candida
albicans, Cryptococcus neoformans, Aspergillus flavus, Aspergillus
fumigatus, Coccidioides, Paracoccidioides, Histoplasma or
Blastomyces. Other exemplary fungal associated disorders include
oral thrush, vaginal candidiasis, aspergillosis, candidosis,
chromomycosis, coccidioidiocycosis, cryptocococcosis,
entomophthoromycosis, epizootic lymphangitis, geotrichosis,
histoplasmosis, mucormycosis, mycetoma, north american
blastomycosis, oomycosis, paecilimycosis, penicilliosis,
rhinosporidiosis, and sprotrichiosis in animals.
[0054] Specifically, the infectious inflammatory disease of the
present invention may be at least one selected from the group
consisting of salmonellosis, food poisoning, typhoid, paratyphoid,
sepsis, septic shock, systemic inflammatory response syndrome
(SIRS), multiple organ dysfunction syndrome (MODS), pneumonia,
pulmonary tuberculosis, tuberculosis, cold, influenza, airway
infection, rhinitis, nasopharyngitis, otitis media, bronchitis,
lymphadenitis, mumps, adenolymphitis, cheilitis, stomatitis,
arthritis, myositis, dermatitis, vasculitis, gingivitis,
pericementitis, keratitis, conjunctivitis, wound infection,
peritonitis, hepatitis, osteomyelitis, cellulitis, meningitis,
encephalitis, brain abscess, encephalomyelitis, cerebral
meningitis, osteomyelitis, nephritis, carditis, endocarditis,
enteritis, gastritis, esophagitis, duodenitis, colitis, urinary
tract infection, cystitis, vaginitis, cervicitis, salpingitis,
infectious erythema, bacterial dysentery, abscess and ulcer,
bacteremia, diarrhea, dysentery, gastritis, gastroenteritis,
genitourinary abscess, open wound or wound infection, purulent
inflammation, abscesses, boils, pyoderma, impetigo, folliculitis,
cellulitis, wound infection after surgery, scalded skin syndrome,
skin burn syndrome, thrombotic thrombocytopenia, hemolytic uremic
syndrome, renal failure, pyelonephritis, glomerulonephritis,
nervous system abscess, otitis media, sinusitis, pharyngitis,
tonsillitis, mastoiditis, soft tissue inflammation, dental
infection, dacryocystitis, pleurisy, abdominal abscess, liver
abscess, cholecystitis, spleen abscess, pericarditis, myocarditis,
placentitis, amniotic fluid infection, mammitis, mastitis,
puerperal fever, toxic shock syndrome, lyme disease, gas gangrene,
atherosclerosis, Mycobacterium avium syndrome (MAC),
enterohaemorrhagic Escherichia coli (EHEC) infection,
enteropathogenic Escherichia coli (EPEC) infection, enteroinvasive
Escherichia coli (EIEC) infection, methicillin-resistant
Staphylococcus aureus (MRSA) infections, vancomycin-resistant
Staphylococcus aureus (VRSA) infections and listerosis.
[0055] Escherichia is a gram-negative bacillus with eight species
belonging to the Enterobacteriaceae family. Although most bacteria
in Escherichia genus has symbiotic relationship with host and are
harmless to hosts, they are a major cause of urinary tract
infections and cause a variety of gastrointestinal diseases. E.
coli is the most common pathogenic bacterium of Escherichia. In
addition, E. fergusonii infected open wounds or wounds, causing
bacteremia and urinary tract infection, and E. vulneris also mainly
infect wounds.
[0056] E. coli is further divided into 190 serotypes according to
the O, H and K antigens. The pathogenic Escherichia coli is
classified into enterotoxigenic E. coli (ETEC), which produces
enterotoxin, enterohemorrhagic E. coli (EEEC), which produces
verotoxin, enteroinvasive E. coli (EIEC), which invades epithelial
cells of the intestinal mucosa and causes tissue infection, and
Enteropathogenic E. coli (EPEC), which causes acute
gastroenteritis, and enteroaggregative E. coli (EAggEC). Intestinal
hemorrhagic Escherichia coli causes hemorrhage and severe abdominal
pain, rarely thrombotic thrombocytopenia or hemolytic uremic
syndrome, and may cause severe renal failure. This class of
Escherichia coli infection is called hemorrhagic colitis because of
the symptoms of severe hemorrhagic diarrhea. Especially E. coli
O157: H7 is a major food poisoning causative organism. Toxic E.
coli is a causative organism of enteritis and traveler's diarrhea,
causing diarrhea with dehydration. Escherichia coli is a major
symptom of fever and abdominal pain. It infects the epithelial
cells of the large intestine mucosa and causes infection.
Therefore, ulcers are formed by cell necrosis and cause diarrhea,
which is a mixture of blood and mucus. Intestinal pathogenic
Escherichia coli exhibits symptoms of vomiting, abdominal pain,
diarrhea, and fever. Escherichia coli is an infection mainly
through patients, carriers, and animal excreta, but any food
contaminated with bacteria can be a causative agent due to a wide
range of distribution such as livestock, people, and natural
environment.
[0057] It is known that Listeria is a gram-positive bacterium of
even and short shape, and there are 10 species of Listeria. Only L.
monocytogenes and L. ivanovii are the pathogens, and it is known
that only L. monocytogenes is able to infect humans.
[0058] Listeria is mainly transmitted through contaminated food,
and may be directly transmitted from an infected animal Listeriosis
often manifests as a fever or sepsis, such as high fever, myalgia,
and can cause meningitis, encephalitis, brain abscess, etc. in the
central nervous system. Infection with gastrointestinal tract
causes symptoms such as fever, nausea and vomiting. It is rarely
seen as a local infection such as soft tissue, conjunctivitis,
pleuritis, peritonitis, hepatitis, hepatic abscess, cholecystitis,
spleen abscess. It can cause major infectious symptoms such as
sepsis or meningitis, and peritonitis, endocarditis, and brain
abscess in patients with decreased cellular immunity, organ
transplant recipients undergoing immunosuppressive treatment,
elderly, and pregnant women. Pregnant women cause bacteremia
similar to that of influenza. Unless they are treated early, they
can cause placenta, sheep, and fetal infections, leading to
miscarriage or stillbirth. Healthy adults can also cause
gastroenteritis.
[0059] Salmonella is a rod-shaped gram negative bacillus belonging
to the Enterobacteriaceae family. Salmonella genus is classified
into two species, Salmonella enterica (S. enterica) and Salmonella
bongori (S. bongori), and S. enterica again divided into six
subspecies. It is composed of about 2,500 serotypes again according
to the combination of the bacterial antigen (O) and the flagella
antigens (H), which are salmonella lipopolysaccharide. Many
Salmonella serotypes, including S. typhi, S. enteritidis, S.
paratyphi, S. typhimurium, and S. choleraesuis, which cause
infectious diseases in humans, belong to enterica subspecies.
[0060] Salmonella infects humans and animals through various routes
including contaminated food, infected animals, water, and utensils,
and causes disease. Salmonella infection is caused by various
symptoms such as food poisoning, enteritis, sepsis, bacteremia,
chronic infection and local infection. Especially in humans S.
typhi causes typhus, S. paratyphi causes paratyphi, S. typhimurium,
S. enteritidis, S. Infantis, S. heidelberg, etc. cause
gastroenteritis. Salmonellosis causes gastrointestinal symptoms
such as fever, headache, abdominal pain, diarrhea, nausea,
vomiting, and dehydration through a latent period of 12 to 36
hours. It begins with acute enterocolitis and may progress to
sepsis or bacteremia, abscess, arthritis, cholecystitis,
pericarditis, pneumonia, syphilis, pyelonephritis. Salmonella can
be transmitted through any tissue of the body.
[0061] Staphylococcus is a gram-positive bacterium that has single,
double or irregular grape arrangement. Staphylococcus is classified
into about 40 species, and again divided into 11 groups according
to the 16s ribosomal RNA (rRNA) base sequence. Among them, S.
aureus, S. epidermidis, and S. saprophyticus are the main problems
in clinical practice.
[0062] S. aureus is a major causative agent of pyogenic
inflammation and has various infectious symptoms ranging from food
poisoning to sepsis. It has been shown that various toxins such as
coagulase and enterotoxin, which have potent toxicity to coagulate
plasma. Protein A, an intracellular component of S. aureus, acts on
complement activation, localized swelling and seizure. The symptoms
of S. aureus infection include the skin infection, such as
folliculitis, burns, infections, impetigo, post-operative wound
infections, and skin lethargy syndromes, bloodstream infection,
pneumonia, arthritis, acute endocarditis, myocarditis,
encephalitis, meningitis, genitourinary tract, nervous system,
abdominal abscess, otitis media, conjunctivitis, toxic shock
syndrome. Furthermore, S. aureus, which is resistant to
antibiotics, is particularly difficult to treat and is a trifling
problem in opportunistic infections and disease management in
hospitals, schools, and prisons. They are methicillin-resistant
Staphylococcus aureus (MRSA), which is resistant to beta-lactam
antibiotics such as penicillin and methicillin,
vancomycin-intermediate S. aureus (VISA), which is resistant to the
glycoprotein antibiotic vancomycin, heterogenous
vancomycin-intermediate S. aureus (hVISA) and high-level
vancomycin-resistant S. aureus (VRSA), and the like. S.
epidermidis, which is another coagulase negative pathogen of
Staphylococcus sp. causes a pathogenic infectious disease that can
be infected by therapeutic instruments, and S. saprophyticus causes
urinary tract infection.
[0063] The present invention also provides a food composition for
preventing or ameliorating infectious inflammatory diseases
comprising tryptophanyl-tRNA synthetase as an active ingredient.
The tryptophanyl-tRNA synthetase may be any one selected from the
group consisting of SEQ ID NO: 1 to SEQ ID NO: 8.
[0064] The food composition according to the present invention
includes all forms of functional food, nutritional supplement,
health food and food additives. These types can be prepared in
various forms according to conventional methods known in the
art.
[0065] For example, as a health food, the food composition itself
according to the present invention can be prepared in the form of
tea, juice, and drink. Also it can be eaten in granulated,
encapsulated, or powdered form. In addition, the food composition
according to the present invention may be prepared in the form of a
composition by mixing with known substances or active ingredients
known to be effective for immune enhancement or for the prevention
or improvement of diseases caused by bacterial infection.
[0066] Functional foods also can be prepared by adding the food
composition according to the present invention to beverages
(including alcoholic beverages), fruits and processed foods (such
as canned fruits, bottled fruits, jam, marmalade), fish, meat and
its processed foods (e.g., ham, sausage etc), breads and noodles
(e.g., udon, buckwheat noodles, ramen noodles, spaghetti, macaroni,
etc.), fruit juice, various drinks, cookies, taffy, dairy products
(e.g., butter, cheeses etc.), edible vegetable oils, margarine,
vegetable protein, retort food, frozen food, various kinds of
seasoning (e.g., soybean paste, soy sauce, sauce, etc.).
[0067] The preferable content of the food composition according to
the present invention is not limited to this, but is preferably
0.01 to 50% by weight in the finally prepared food. In order to use
the composition for food according to the present invention in the
form of a food additive, it may be used in the form of powder or
concentrate.
[0068] The present invention also provides a veterinary composition
for treating or preventing inflammatory diseases caused by
infection comprising tryptophanyl-tRNA synthetase as an active
ingredient. The tryptophanyl-tRNA synthetase may be any one
selected from the group consisting of SEQ ID NO: 1 to SEQ ID NO:
8.
[0069] In animals, E. coli mainly causes colibacillosis by
intestinal infections in cattle, pigs, and chickens, and causes
gastrointestinal disorders such as diarrhea and atrophy of calves
and uterine myositis of cattle, sepsis of pigs, diarrhea,
intestinal diseases, dehydration, neurological symptoms and the
like.
[0070] Salmonella has poultry, pigs, cows, iguanas, turtles, dogs,
cats, pets, livestock and wild animals as a hospital. Salmonellosis
in animals is an acute or chronic digestive infectious disease of
livestock, mainly in cattle and swine. It often occurs in calves
and is characterized by fever, enteritis, and sepsis. It can cause
pneumonia, encephalitis, arthritis, and mastitis. The salmonellosis
in pigs are often called pig paratyphoids because they cause
symptoms such as gastroenteritis sepsis in the frying period. S.
gallinarum, a serotype of Salmonella, causes fowl typhoid in
chickens resulting in high mortality from sepsis.
[0071] In animals, Listeria infects a variety of livestock and
wildlife, including chickens, cows, pigs, dogs, raccoons, goats,
sheep, and mice. Listeriosis mainly causes abortion, sepsis,
meningitis, encephalitis, etc. in ruminant animals, and it is also
referred to as a circulatory disease, in which the bacterium
invades the brain tissue and causes damage to the nerve cells, such
as circling movement or rushing into obstacles. Staphylococcus is
one of the common causative bacteria for bacterial infections in
animals. It induces purulent diseases such as inflammation of the
skin and soft tissues, and mastitis in ruminants such as cattle,
sheep and goats.
[0072] The veterinary compositions of the present invention may
further comprise suitable excipients and diluents according to
conventional methods. Excipients and diluents that may be included
in the veterinary composition include lactose, dextrose, sucrose,
sorbitol, mannitol, xylitol, erythritol, maltitol, starch, acacia
rubber, alginate, gelatin, calcium phosphate, calcium silicate,
cellulose, methylcellulose, microcrystalline cellulose,
polyvinylpyrrolidone, water, methylhydroxybenzoate,
propylhydroxybenzoate, talc, magnesium stearate, cetanol, stearyl
alcohol, liquid paraffin, sorbitan monostearate, poly Sorbate 60,
methylparaben, propylparaben, and mineral oil.
[0073] The veterinary composition of the present invention may
further comprise fillers, anti-coagulants, lubricants, wetting
agents, spices, emulsifiers, preservatives, and the like. The
veterinary composition according to the present invention can be
formulated using methods well known in the art so as to provide
rapid, sustained or delayed release of the active ingredient after
administration to the animal. And the formulations may be in the
form of powders, granules, tablets, capsules, suspensions,
emulsions, solutions, syrups, aerosols, soft or hard gelatine
capsules, suppositories, sterile injectable solutions, sterile
external preparations and the like.
[0074] The veterinary composition according to the present
invention may vary depending on the type of animal, age, sex, and
body weight, but may be administered in an amount of 0.1 to 100
mg/kg once or several times a day. The dose may also be increased
or decreased depending on the route of administration, degree of
disease, sex, weight, age, and the like. Accordingly, the dose does
not in any way limit the scope of the invention.
[0075] The present invention also provides a composition for immune
enhancement comprising tryptophanyl tRNA synthetase as an active
ingredient. The tryptophanyl-tRNA synthetase may be any one
selected from the group consisting of SEQ ID NO: 1 to SEQ ID NO:
8.
[0076] Immune enhancement means increasing the immune response or
activity of the in vivo immune system. The composition of the
present invention is effective for alleviating the immune function
deterioration due to aging, pregnancy, immunosuppressive treatment
or the like, or for preventing and improving diseases caused by
immune dysfunction. The disease caused by the immune function
deterioration is preferably one selected from the group consisting
of a viral infectious disease such as a cold, an allergic disease
such as an inflammatory disease, an atopy, chronic fatigue, and
cancer, but is not limited thereto. And all diseases caused by
immune function deterioration known to those skilled in the art are
included in the present invention. The composition of the present
invention may also be included as an adjuvant of a vaccine.
[0077] The present invention provides a method for preventing,
ameliorating or treating infectious inflammatory diseases
comprising administering to a subject in need thereof an effective
amount of tryptophanyl-tRNA synthetase as an active ingredient.
[0078] The present invention provides a use for preparing an agent
for preventing, ameliorating or treating infectious inflammatory
diseases comprising tryptophanyl-tRNA synthetase as an active
ingredient.
[0079] The present invention provides a method for immune
enhancement comprising administering to a subject in need thereof
an effective amount of tryptophanyl-tRNA synthetase as an active
ingredient.
[0080] The present invention provides an application for preparing
an agent for immune enhancement containing tryptophanyl-tRNA
synthetase as an active ingredient.
[0081] The said "effective amount" of the compound of the present
invention refers to an amount which, when administered to a
subject, indicates an improvement, treatment and prophylactic
effect of infectious inflammatory diseases, and the said "subject"
may be an animal, preferably a mammal, particularly a human, animal
including livestock, or may be an animal derived cell, tissue,
organ, or the like. The subject may be a patient or a domestic
animal requiring treatment.
Advantageous Effect
[0082] Accordingly, the present invention provides a pharmaceutical
composition and a veterinary composition for treatment or
prevention of infectious inflammatory diseases comprising
tryptophanyl-tRNA synthetase as an active ingredient, a food
composition for prevention and improvement, and a composition for
immune enhancement, which comprises tryptophanyl-tRNA synthetase as
an active ingredient. The composition of the present invention is
particularly useful for preventing or treating diseases of humans
and animals caused by bacterial, viral or fungal infections by
inhibiting infections such as bacteria and viruses at an early
stage by activating innate immune responses.
BRIEF DESCRIPTION OF DRAWINGS
[0083] The patent or application file contains at least one drawing
executed in color. Copies of this patent or patent application
publication with color drawing(s) will be provided by the Office
upon request and payment of the necessary fee.
[0084] FIG. 1A shows the result of western blot analysis of TrpRS
(WRS) of human peripheral blood mononuclear cell supernatant (SUP)
and whole cell lysate (WCL) infected with S. typhimurium, and FIG.
1B shows the result of ELISA for the representative amount of
TrpRS, HMGB-1 and HSP70 protein in culture supernatant of human
peripheral blood mononuclear cells infected by bacteria and
fungi.
[0085] FIG. 2A shows the result of western blot analysis showing
the secretion pattern of tryptophanyl-tRNA synthetase (TrpRS),
tumor necrosis factor alpha (TNF-.alpha.), HMGB-1 and HSP70
secreted by S. typhimurium-infected human peripheral blood
mononuclear cells over time, and FIG. 2B shows the results of ELISA
showing the measurement of TNF-.alpha. and TrpRS produced in the
culture supernatant of human peripheral blood mononuclear cells
infected with S. typhimurium over time.
[0086] FIG. 3 shows a result of lactate dehydrogenase (LDH) assay
to determine whether pyroptosis occurs in human peripheral blood
mononuclear cells infected with S. typhimurium.
[0087] FIG. 4 shows real time-PCR results showing the mRNA levels
of TNF-.alpha. and TrpRS produced in human peripheral blood
mononuclear cells infected with S. typhimurium over time.
[0088] FIG. 5 shows the results of TrpRS antibody treatment and
ELISA test to examine the effect of TrpRS on the secretion of
TNF-.alpha. in human peripheral blood mononuclear cells infected
with S. typhimurium.
[0089] FIG. 6A shows the amount of TrpRS (WRS) protein in the
culture supernatant of human peripheral blood mononuclear cells
infected with respiratory syncytial virus (RSV) and FIG. 6B shows
human peripheral blood mononuclear cells infected with PR8
influenza virus, respectively. The results obtained by ELISA are
shown.
[0090] FIG. 7 shows ELISA results showing the secretion pattern of
TNF-.alpha. and MIP-1.alpha. in TrpRS-treated immune cells.
[0091] FIG. 8A shows that the secretion amounts of MIP-1.alpha.,
TNF-.alpha., MIP-113, IL-6 and IL-8 were analyzed using image Lab
4.1 software after treating PBMC cells with full length-TrpRS and
mini-TrpRS; FIG. 8B shows results of ELISA; and FIG. 8C shows
RT-PCR for confirming the expression levels of TNF-.alpha.,
MIP-1.alpha. and MIP-1.beta. in cultured supernatant cultured in
PBMC.
[0092] FIG. 9 shows the results of a transwell migration assay
showing the effect of the culture supernatant of TrpRS-treated bone
marrow-derived macrophages (BMDM) on the immune cell fluidity.
[0093] FIG. 10A-C shows the results of ELISA for the amount of
MIP-1.alpha. in PBMC-derived macrophages, THP-1 cells, THP-1
derived macrophages and J774A.1 cells, and the amount of
TNF-.alpha., MIP-1.alpha. MCP-1 protein as determined by ELISA and
RT-PCR, respectively.
[0094] FIG. 11A-D shows the result of flow cytometry analysis
showing the neutrophil recruitment in the mouse peritoneal cavity
injected with TrpRS, the result of ELISA showing the secretion
amount of MIP1-.alpha., and the results of flow cytometric analysis
showing the number of neutrophil, macrophage, and bone marrow
cells.
[0095] FIG. 12A-B shows flow cytometric analysis results showing
CD40, CD80, and CD86 protein expression patterns of TrpRS-treated
bone marrow-derived macrophages.
[0096] FIG. 13 shows the results of macrophage experiments using
fluorescently-labeled Escherichia coli derived from the
phagocytosis index of TrpRS-treated bone marrow-derived
macrophages.
[0097] FIG. 14A-B shows the results of measurement of the amount of
TNF-.alpha. and MIP-1.alpha. in the full length-TrpRS and
mini-TrpRS-treated macrophages by ELISA, and the results of
measurement of the number of CD11b.sup.+ F4/80.sup.+ cells in PEC
(peritoneal exudate cells) and Ly6G.sup.+ neutrophils by flow
cytometry.
[0098] FIG. 15A-B shows the images (X20) obtained by injecting the
full length-TrpRS and mini-TrpRS (red) labeled with Alexa 647 in
the LysM-GFP transgenic mice, and the index of macrophage in the
mice infected with S. typhimurium, which were injected with full
length-TrpRS and mini-TrpRS.
[0099] FIG. 16 schematically shows a process for producing an
antibody specifically binding to TrpRS.
[0100] FIG. 17A-C shows the amount of TNF-.alpha. in THP-1 cells
treated with full length-TrpRs and antibodies specific to TrpRS,
the results of ELISA showing the effect of antibody (scFv 4G1) on
TNF-.alpha. production in human PBMC cells, and the expression of
recombinant protein binding to full length-TrpRS or mini-TrpRS
using antibodies.
[0101] FIG. 18A-C shows a schematic diagram of an animal experiment
using an antibody; the effect of the antibody on the expression of
TNF-.alpha. and MIP-1.alpha. and the effect on the number of
Ly6G.sup.+ neutrophils.
[0102] FIG. 19 shows a survival plot showing the effect of
antibodies specific to TrpRS on the survival rate of S.
typhimurium-infected mice.
[0103] FIG. 20 shows the overviews of animal experiments to
investigate the effect of TrpRS on the survival rate of mice
infected with S. typhimurium (top in FIG. 20) and the results of
flow cytometry showing the effect of TrpRS on the degree of S.
typhimurium-adsorption or -absorption in infiltrating
neutrophils.
[0104] FIG. 21A-B shows a schematic diagram of animal experiments
and shows the results of measuring IHC and CFU in the liver and
spleen of mice, which were administered intraperitoneally with
PBS(Con), FL-WRS, or mini-WRS (each 20 mg/mouse) 1 hour before the
infection with S. typhimurium or L. monocytogenes.
[0105] FIG. 22A-B shows a survival plot showing the effect of TrpRS
on the survival rate of S. typhimurium-infected mice.
DETAILED DESCRIPTION OF THE INVENTION
[0106] Hereinafter, the present invention will be described in
detail.
[0107] However, the following examples are illustrative of the
present invention, and the scope of the present invention is not
limited to the following examples.
Example 1
The Tryptophanyl-tRNA Synthetase (TrpRS) Secreted from Bacterial
Infected Peripheral Blood Mononuclear Cells
Example 1-1. Identification of Aminoacyl-tRNA Synthetase Secreted
from Bacterial and Fungal Infected Human Peripheral Blood
Mononuclear Cells
[0108] Immunoblot experiments were conducted to determine the type
of aminoacyl-tRNA synthetase (ARS) secreted from human peripheral
blood mononuclear cells (PBMC) infected with bacteria (FIG. 1).
Bacteria and fungi, Salmonella typhimurium (S. typhimurium, ATCC
14028), Listeria monocytogenes (L. monocytogenes, ATCC 15313),
Escherichia coli (E. coli, ATCC 10798), Staphylococcus aureus (S.
aureus, ATCC 25923), Candida albicans (C. albicans, ATCC 10231),
were obtained from the Korea Microbial Conservation Center and the
Microbiological Resource Center, and were cultured periodically in
nutrient broth or brain heart infusion (BD biosciences). The
bacteria used for the infection experiment were cultured overnight,
and were obtained at a density of 1.times.10.sup.8 CFU. The CFU was
estimated using an absorbance at 600 nm and a calibration curve
prepared beforehand. In the bacterial infection experiment of this
example and another example, the obtained bacteria were washed in
PBS and resuspended in serum-free RPMI medium or PBS. Human PBMC
were cultured at a density of 1.times.10.sup.6 cells/well for one
hour and infected with 1.times.10.sup.6 CFU of S. typhimurium
(MOI=1) or L. monocytogenes (MOI=1). The supernatants cultured for
two hours after infection were precipitated by TCA and immunoblot
experiments were performed on various kinds of ARS.
[0109] As a result, the only full-length TrpRS, 53 kDa, was
detected in the culture supernatant among the ARSs including
secretory ARS (TrpRS, GRS, KRS, DRS), AIMP1 (a cofactor of ARS
complexes) and ARS (TrpRS, MRS, HRS, GRS) containing the WHEP
domain. This shows that the ARS secreted after bacterial infection
is TrpRS (WRS) (FIG. 1A). It was also confirmed that full-length
WRS was secreted from human peripheral blood mononuclear cells by
infection with S. typhimurium and L. monocytogenes as well as by E.
coli, S. aureus and C. albicans (FIG. 1B). This indicates that
TrpRS (WRS) is more likely to be secreted in response to general
bacterial and fungal infections than to certain bacteria.
Example 1-2. Kinetic Analysis of TrpRS and TNF-.alpha.
Secretion
[0110] The secretion patterns of tryptophanyl-tRNA synthetase
(TrpRS), tumor necrosis factor alpha (TNF-.alpha.), HMGB1, and heat
shock protein (HSP70) was analyzed in human peripheral blood
mononuclear cells (PBMC) infected with S. typhimurium from time to
time right after infection (FIG. 2). Human PBMC were infected with
S. typhimurium (MOI=1), and whole cell lysate (WCL) and culture
supernatant were obtained at 0, 15, 30, 60, and 120 min, and
immunoblot experiments were performed (FIG. 2A).
[0111] As a result, TrpRS in cultured supernatants was detected
from 15 minutes after infection and increased for up to 120 minutes
after infection. Also, the amount of TrpRS in WCL tended to
decrease slightly with time after infection. Therefore, TrpRS is
secreted to the outside of the cell from the beginning after
infection. In addition, in the whole cell lysate, the TNF-.alpha.
precursor (precursor TNF-.alpha.) was generated from 30 minutes
after infection and was detected at 120 minutes, TNF-.alpha.
(Mature TNF-.alpha.) was detected in trace amounts up to 120
minutes after infection. TNF-.alpha. (Mature TNF-.alpha.) was
detected in the culture supernatant at 120 min. In other words,
TrpRS is secreted to the outside of the cell within a short time
after the infection, and it is found that it significantly precedes
the secretion of TNF-.alpha. in time.
[0112] On the other hand, HMGB-1 and HSP70 were not detected in the
culture supernatant over time after infection, whereas HMGB-1 and
HSP 70 in all cell lysates were constantly detected with time after
infection. Thus, HMGB-1 and HSP70 are not affected by bacterial
infection.
[0113] In addition, the amounts of TrpRS and TNF-.alpha. secreted
in the culture supernatant after bacterial infection were measured
by ELISA at 0, 15, 30, 60, and 120 min after infection (FIG. 2B).
As observed in the immunoblot experiment, TrpRS present in the
culture supernatant increased significantly from 15 minutes after
infection to 60 minutes after infection, but TNF-.alpha. present in
the culture supernatant started to increase from 60 minutes after
infection.
Example 1-3. Determination for Bacterial Infection and
Pyroptosis
[0114] It was investigated whether TrpRS secretion in human
peripheral blood mononuclear cells (PBMC) infected with S.
typhimurium observed in Example 1-2 was caused by pyroptosis (FIG.
3). The pyroptosis was confirmed by assay of lactate dehydrogenase
(LDH; a signature of cell death). In detail, human PBMCs were
infected with S. typhimurium, and then LDH levels in culture
supernatants at 0, 5, 10, 20, 40, 60, and 120 min after infection
were measured using the LDH assay kit (Takara Bio, Inc.). 1% TX-100
treated PBMC was used as a positive control.
[0115] As a result, in the culture supernatant of the positive
control (1% TX-100), the amount of LDH, a marker of pyroptosis,
increased rapidly with time, whereas the culture supernatant of S.
typhimurium-infected PBMC reached 120 minutes after infection with
no significant change in the amount of LDH, indicating that LDH was
not expressed during this period. Therefore, these results verify
that PBMC after bacterial infection excretes TrpRS outside the cell
by active secretion rather than pyroptosis (FIG. 3).
Example 1-4. Evaluation on Bacterial Infection and Expression
Levels of TNF-.alpha. and TrpRS
[0116] The expression patterns of TNF-.alpha. and TrpRS (WRS) genes
in human peripheral blood mononuclear cells (PBMC) infected with S.
typhimurium were examined by RT-PCR and ELISA (FIG. 4). Human PBMC
were infected with S. typhimurium, and cells were obtained at 0,
15, 30, 60, 120 minutes after the infection, and the mRNA levels of
TNF-.alpha. and TrpRS were measured. RNA was extracted according to
the experimental method of RNeasy kit (Qiagen, Hilden, Germany) and
reverse transcribed with M-MLV reverse transcriptase (Invitrogen,
Carlsbad, Calif., USA), then quantitative real-time PCR
(quantitative RT-PCR) was performed with the following primers. The
level of GAPDH mRNA was determined as an internal control.
TABLE-US-00001 hTNF-.alpha. Forward: (SEQ ID NO: 9)
5-GGAGAAGGGTGACCGACTCA-3 hTNF-.alpha. Reverse: (SEQ ID NO: 10)
5-CTGCCCAGACTCGGCAA-3 hTrpRS Forward: (SEQ ID NO: 11)
5-AAGAATTCATGCCCAACAGTGAGCCC-3 hTrpRS Reverse: (SEQ ID NO: 12)
5-AACTCGAGCTACCCTGGAGGACAGTCAGCCTT-3 GAPDH forward: (SEQ ID NO: 13)
5-CGCTCTCTGCTCCTCCTGTTC-3 GAPDH reverse: (SEQ ID NO: 14)
5-TTGACTCCGACCTTCACCTTCC-3
[0117] As a result, it was confirmed that the level of TNF-.alpha.
mRNA increased from 30 minutes to 120 minutes, while the level of
TrpRS mRNA did not significantly change until 120 minutes after
infection (FIG. 4). This suggests that TrpRS secreted after
infection is one, which is already present in the cell without its
gene expression induced after infection. It was also confirmed that
mRNA of TNF-.alpha., a major proinflammatory cytokine induced by
bacterial infection, increased greatly from 30 minutes to 12
minutes after infection. The TNF-.alpha. mRNA was significantly
increased up to 60 minutes after 40 minutes of infection and the
increase in the amount of TNF-.alpha. secretion observed in Example
1-2 was detected from 60 minutes after the infection, indicating
that the secretion of TrpRS is already occurring before TNF-.alpha.
production.
Example 1-5. Relationship Between TrpRS and TNF-.alpha. Secreted
after Bacterial Infection
[0118] In Example 1-2, it was confirmed that TrpRS and TNF-.alpha.
were secreted with time difference in S. typhimurium-infected human
peripheral blood mononuclear cells (PBMC). In addition, it was
observed that TNF-.alpha. was not secreted in the absence of TrpRS
secretion at the early stage of infection in the PBMC infected with
Heat-killed S. typhimurium. Thus, the functional relationship
between TrpRS secreted after infection and TNF-.alpha. was examined
(FIG. 5). PBMCs were treated with TrpRS function-neutralizing
antibody (antibody concentration 10 .mu.g/mL) and infected with S.
typhimurium (MOI=1). Then the secretion pattern of TNF-.alpha. was
measured at 0, 2, 4, and 8 h, by ELISA.
[0119] As a result, in PBMC (S. typhimurium+.alpha.-WRS ScFv),
which had reduced the function of TrpRS by antibody treatment, it
was observed that the amount of TNF-.alpha. was significantly
decreased compared with PBS-treated control PBMC (S.
typhimurium+PBS). This suggests that TrpRS plays an important role
in the production and secretion of TNF-.alpha.. These results
suggest that TrpRS may be the first factor to control TNF-.alpha.
production, especially in bacterial infections.
Example 1-6 Aminoacyl t-RNA Synthetase Secreted from Virus-Infected
Human Peripheral Blood Mononuclear Cells
[0120] ELISA experiments were performed to determine the amount of
aminoacyl t-RNA synthetase (ARS) secreted by human peripheral blood
mononuclear cells (PBMC) over time after viral infection (FIG. 6).
The virus was titrated by respiratory syncytial virus A2 (RSV A2)
and PR8 influenza virus (Influenza A/Puerto Rico/8/1934 virus) by
standard plaque analysis. Human PBMCs were each infected with the
human PBMC for 2 hours and incubated for 24 hours. Culture
supernatants were harvested at each hour post-infection and levels
of TrpRS (WRS) were measured by ELISA.
[0121] As a result, the concentration of TrpRS increased with time
in RSV-infected cells (FIG. 6A), while in the PR8-infected cells,
the TrpRS concentration increased up to 120 minutes after infection
but decreased after 120 minutes (FIG. 6B). This shows that TrpRS is
secreted in response to viral infection.
Example 2
Increased Secretion of Monocyte/Macrophage-Specific TNF-.alpha. and
MIP1-.alpha. by TrpRS
[0122] To investigate the types of immune cells responsive to
secreted TrpRS, various immune cells were treated with TrpRS and
cells that secrete cytokines such as TNF-.alpha. and MIP1-.alpha.
were examined (FIG. 7). Primary B cells, T cells, neutrophils,
natural killer cells (NK), and peripheral blood mononuclear cells
(NK) and monocyte of mice were isolated using a mouse microbead
isolation kit (Miltenyi, Bergisch Gladbach, Germany). The obtained
cells showed more than 95% purity when analyzed by flow cytometry.
Bone marrow-derived macrophages (BMDM) were prepared by
differentiating for 6 to 7 days in the presence of M-CSF (20
ng/mL). Bone marrow-derived dendritic cells (BMDC) were prepared by
differentiating for 6 to 7 days in the presence of GM-CSF (20
ng/ml) and IL-4 (20 ng/ml) Immunocytes were cultured for 18 hours
in the presence of the control, full-length TrpRS (TrpRS-full, 100
nM), mini-TrpRS (TrpRS-mini, 100 nM), and LPS (100 ng/ml),
respectively, and the amount of TNF-.alpha. and MIP1-.alpha.
protein present in the culture supernatant was measured by ELISA
kit (BD Sciences, San Jose, Calif., USA and R & D systems).
TrpRS all used a protein having the amino acid sequence of human
TrpRS (human TrpRS) in the experiment.
[0123] As a result, LPS significantly induced TNF-.alpha. secretion
in most of the immune cells, whereas full-length TrpRS showed the
greatest effect in monocytes and BMDM (Table 1, top of FIG. 7).
Full-length TrpRS treated with heat or trypsin had no effect on
TNF-.alpha. secretion (data not shown). In addition, mini-TrpRS had
no effect on TNF-.alpha. secretion. For MIP1-.alpha., the increase
effect of TrpRS was confirmed only in monocytes and BMDM of mice
treated with full-length TrpRS (Table 2, FIG. 7 bottom). These
results indicate that TrpRS specifically activates monocytes and
macrophages, and monocytes and macrophages secrete TNF-.alpha. and
MIP1-.alpha. as a result of activation.
TABLE-US-00002 TABLE 1 Effect of TrpRS on the secretion of
TNF-.alpha. in immune cells TNF-.alpha. Full-length Mini (pg/mL)
Control TrpRS TrpRS LPS B cell 107 .+-. 91 132 .+-. 34 79 .+-. 44
227 .+-. 38 CD4+ T cell -2 .+-. 4 99 .+-. 20 134 .+-. 125 516 .+-.
4 Monocyte 69 .+-. 7 511 .+-. 43 10 .+-. 13 975 .+-. 24 BMDM 17
.+-. 11 3299 .+-. 175 44 .+-. 35 3573 .+-. 7 BMDC 61 .+-. 11 1083
.+-. 105 148 .+-. 119 3557 .+-. 66 Neutrophil 2.1 .+-. 4 597 .+-.
38 65 .+-. 4 3765 .+-. 130 NK 2.8 .+-. 8 259 .+-. 14 3 .+-. 8 2373
.+-. 200
TABLE-US-00003 TABLE 2 Effect of TrpRS on the secretion of
MIP1-.alpha. in immune cells MIP1-.alpha. Full-length Mini (pg/mL)
Control TrpRS TrpRS LPS B cell 57 .+-. 2 124 .+-. 2 85 .+-. 23 391
.+-. 49 CD4+ T cell 8 .+-. 1 141 .+-. 13 9 .+-. 1 552 .+-. 7
Monocyte 7 .+-. 0 533 .+-. 27 6 .+-. 1 1246 .+-. 7 BMDM 7 .+-. 7
2647 .+-. 205 8 .+-. 1 3369 .+-. 46 BMDC 32 .+-. 5 34 .+-. 34 50
.+-. 16 980 .+-. 78 Neutrophil 6 .+-. 3 28 .+-. 3 7 .+-. 5 3529
.+-. 8 NK 6 .+-. 3 36 .+-. 1 3 .+-. 1 1157 .+-. 41
Example 3
Activation of Innate Immune Response by TrpRS
Example 3-1. Chemokines Secreted by TrpRS-Stimulated Bone
Marrow-Derived Macrophages
[0124] The types and amounts of chemokines secreted by BMDM in
response to TrpRS were examined (Table 3). BMDM was treated with
full-length TrpRS (30, 100 nM) or mini-TrpRS (100 nM) for 18 hours,
and the presence of chemokines in the culture supernatant was
measured by ELISA.
[0125] In addition, human PBMC cells were treated with human full
length-TrpRS (FL-WRS) and mini-TrpRS (mini-WRS) for 18 hours and
cytokines present in the culture supernatant were measured using
ELISA. RT-PCR experiments were used to measure the expression
levels of cytokines and chemokines.
TABLE-US-00004 hTNF-.alpha. Forward: (SEQ ID NO: 9)
5-GGAGAAGGGTGACCGACTCA-3 hTNF-.alpha. Reverse: (SEQ ID NO: 10)
5-CTGCCCAGACTCGGCAA-3 hTrpRS Forward: (SEQ ID NO: 11)
5-AAGAATTCATGCCCAACAGTGAGCCC-3 hTrpRS Reverse: (SEQ ID NO: 12)
5-AACTCGAGCTACCCTGGAGGACAGTCAGCCTT-3 hMIP-1.alpha. Forward: (SEQ ID
NO: 15) 5-ACCATGGCTCTCTGCAACCA-3 hMIP-1.alpha. Reverse: (SEQ ID NO:
16) 5-TTAAGAAGAGTCCCACAGTG-3 hMIP-1.beta. Forward: (SEQ ID NO: 17)
5-AGCCTCACCTCTGAGAAAACC-3 hMIP-1.beta. Reverse: (SEQ ID NO: 18)
5-GCAACAGCAGAGAAACAGTGAC-3 GAPDH forward: (SEQ ID NO: 13)
5-CGCTCTCTGCTCCTCCTGTTC-3 GAPDH reverse: (SEQ ID NO: 14)
5-TTGACTCCGACCTTCACCTTCC-3
[0126] As a result, full-length TrpRS induced chemokines such as
MIP-la, MCP-1, and IP-10 and cytokines such as TNF-.alpha. and
IL-113 in a concentration-dependent manner. On the contrary,
mini-TrpRS had no effect on cytokine secretion and chemokine
secretion (Table 3). In addition, full-length TrpRS induced the
secretion of chemokines and cytokines such as TNF.alpha.,
MIP-1.alpha., MIP-1.beta., IL-6 and IL-8, but mini-TrpRS had no
effect on cytokine and chemocyte secretion (FIG. 8A). In addition,
it was confirmed that the expression levels of TNF.alpha.,
MIP-1.alpha., MIP-1.beta., IL-6 and IL-8 were increased in PBMC
cells treated with full length-TrpRS (FIGS. 8B & 8C)
[0127] Thus, it was confirmed that Full length-TrpRS induces the
expression and secretion of cytokines, in contrast to
mini-TrpRS.
TABLE-US-00005 TABLE 3 The cytokines and chemokines secreted by
TrpRS- stimulated bone marrow-derived macrophages (BMDM) Mini
Full-length TrpRS TrpRS Cytokines Control 30 nM 100 nM 100 nM
TNF-.alpha. 17 .+-. 11 2159 .+-. 691 3299 .+-. 175 44 .+-. 35 MIP-1
7 .+-. 7 1621 .+-. 49 2647 .+-. 205 8 .+-. 1 MCP-1 1 .+-. 1 793
.+-. 39 1430 .+-. 114 14 .+-. 19 IP-10 43 .+-. 12 283 .+-. 15 493
.+-. 76 0 .+-. 10 IL-1.beta. 14 .+-. 4 59 .+-. 4 135 .+-. 14 16
.+-. 11
Example 3-2. Effect of TrpRS on Immune Cell Fluidity
[0128] The effect of TrpRS on the fluidity of immune cells was
examined using a transwell migration assay (FIG. 9). Bone
marrow-derived macrophages (BMDM) were treated with full-length
TrpRS (FL-WRS, 100 nM) or mini-TrpRS (mini-WRS, 100 nM) and
cultured for 18 hours, then transferred to a 24-well plate. Primary
immune cells and BMDM were placed in the upper part of the
migration chamber and incubated at 37.degree. C. for 4 hours.
[0129] As a result, it was observed that the culture supernatant of
full-length TrpRS-treated BMDM (TrpRS-F) greatly increased
infiltration of monocytes and neutrophils. In contrast, the TrpRS
protein itself (data not shown) or the mini-TrpRS-treated culture
supernatant (TrpRS-M) had no effect on cell migration.
Example 3-3. Effect of TrpRS on the Secretion of MIP-1 and
TNF-.alpha. in Various Immune Cells
[0130] Effects of TrpRS on secretion of MIP-1 and TNF-.alpha. in
various immune cells including PBMC-derived macrophages, THP-1
cells, THP-1 derived macrophages and J774A.1 cells were
investigated by ELISA experiments and RT-PCR respectively. Each
immune cell was treated with full length-TrpRS (FL-WRS, 100 nM) or
mini-TrpRS (mini-WRS, 100 nM) and cultured for 18 hours. The
culture was transferred to a 96-well plate and subjected to ELISA.
The BMDM cells were treated with full-length TrpRS or mini-TrpRS
and mRNA was extracted and RT-PCR was performed.
[0131] As a result, it was confirmed that full length-TrpRS in
PBMC-derived macrophages, THP-1, THP-1 derived macrophages and
J774A.1 induce the secretion of MIP-1.alpha. (FIG. 10A). In BMDM
cells, it was confirmed that full length-TrpRS, which is not
mini-TrpRS induces the production of TNF-.alpha., MIP-1.alpha. and
MCP-1 proteins (FIG. 10B) and induces mRNA expression (FIG.
10C).
Example 3-4. TrpRS-Induced Neutrophil Accumulation in the Body
[0132] To investigate the effect of TrpRS on the innate immune
response in the body, intraperitoneal neutrophil recruitment
following TrpRS injection was observed (FIG. 11). PBS, full-length
TrpRS (3, 10, 30 .mu.g), or mini-TrpRS (30 .mu.g) were injected
into the peritoneal cavity of mice (6 to 10 per group) and the
peritoneal cavity was drained after 4 hours. The peritoneal
effusion was extracted and the ratio of Ly6C+Ly6G+cell group was
measured by flow cytometry (FIGS. 11A & 11B), and MIP1-.alpha.
present in the peritoneal effusion was measured by ELISA (FIG.
11C). The statistical significance of the comparison between the
PBS-treated negative control and the results of each experimental
condition was verified by one-way Anova test using GraphPad (ver.
4.0) software. ***p<0.001, **p<0.01
[0133] As a result of flow cytometry, concentration-dependent
tendency was dramatically observed only in the full-length TrpRS
injected mice (TrpRS-F3, TrpRS-F10 and TrpRS-F30), whereas
mini-TrpRS (TrpRS-M30) did not achieve this effect (FIG. 11B). That
is, this result shows that full-length TrpRS can induce innate
immune responses that cause neutrophil concentration in vivo.
Similarly, MIP1-.alpha., which was measured in the peritoneal
effusion, increased in a concentration-dependent manner only in the
full-length TrpRS injected mice (TrpRS-F3, TrpRS-F10, and
TrpRS-F30), and did not increase in mini-TrpRS injected mice
(TrpRS-M30).
[0134] In addition, the number of Ly6G.sup.+ neutrophils,
CD11b.sup.+ myeloid cells, and CD11b.sup.+ F4/80.sup.+ macrophages
increased in the full length-TrpRS (FL-WRS) treated peritoneum as
compared to the mini-TrpRS and PBS-infected controls (FIG.
11D).
Example 3-5. Effect of TrpRS on the Activation of Bone
Marrow-Derived Macrophages
[0135] The effect of TrpRS on bone marrow-derived macrophage (BMDM)
activation was analyzed through the expression of activated
macrophage markers and flow cytometry analysis (FIG. 12). Flow
cytometric analysis using Cdllb and F4/80 of FIG. 11A indicates
that bone marrow cells were well differentiated into BMDM for
macrophage activation label analysis. Differentiated BMDM were
treated with full-length TrpRS (30, 100 nM) or mini-TprRS (100 nM)
and cultured for 18 h and CD40, CD80 and CD86 protein expression
levels were measured by flow cytometry.
[0136] As a result, it was confirmed that the cell surface
expression of CD40, CD80 and CD86, which are macrophage activation
indicators, was abruptly increased only in the full-length
TrpRS-treated BMDM (TrpRS-F) (FIG. 12B). The Mini-TrpRS-treated
BMDM (TrpRS-M) was not significantly different from the control
group. That is, this result verifies that full-length TrpRS
promotes activation of macrophages.
Example 3-6. Effect of TrpRS on Phagocytosis of Bone Marrow-Derived
Macrophages (BMDM)
[0137] The effect of TrpRS on the phagocytosis of bone
marrow-derived macrophages (BMDM) was investigated (FIG. 13). BMDM
was cultured in 96-well culture dishes overnight, then replaced
with RPMI medium without M-CSF, and cultured for 18 hours with
full-length TrpRS (30 nM) or mini-TrpRS (30 nM). After washing the
cells, 100 .mu.L of fluorescently labeled E. coli bioparticles
(Vybrant phagocytosis assay kit, Invitrogen) was added and cultured
for 2 hours. After the culture medium was removed, the cells were
treated with trypan blue (100 .mu.L) for 1 minute to inhibit
autofluorescence. Fluorescence signals due to macrophage were
measured at 485 nm (excitation) and 520 nm (emission) to display
the degree of phagocytic action (BMG Labtech, FLUOstar OPTIMA,
Ortenberg, Germany). Statistical significance was verified by
t-test using GraphPad (ver. 4.0) software. ***p<0.0001
[0138] As a result, the phagocytic index of full-length
TrpRS-treated BMDM (TrpRS Full) was found to be 3 times higher than
that of the control group. The Mini-TrpRS (TrpRS Mini) had no
effect. Experimental results of Examples 3-1 to 3-4 show that
full-length TrpRS induces innate inflammatory responses through
macrophage activation.
Example 3-7. Effects of TrpRS on Macrophages
[0139] To investigate the effect of the full length-TrpRS-derived
congenital immune response on macrophages, the following experiment
was carried out using macrophage-depleted mice.
[0140] The splenocytes were removed from the spleen of normal mice
and macrophage-nulled mice and the removal of macrophages was
confirmed by flow cytometry. Separated splenocytes were prepared,
cultured overnight in a 24-well culture dish, and treated with full
length-TrpRS, and the secretion of TNF-.alpha. and MIP-1.alpha. was
measured by ELISA.
[0141] As a result, it was confirmed that the secretion amount of
TNF-.alpha. and MIP-1.alpha. decreased with the decrease of
macrophages (FIG. 14A). The decrease in macrophages in the body
indicates that macrophages play a functional role in the
immunostimulatory activity of full length-TrpRS, as the number of
infiltrated neutrophils in the peritoneum decreases (FIG. 14B).
This confirms that full length-TrpRS targets macrophages to
activate the innate immune response.
Example 3-8. Effect of TrpRS on Macrophage Activity
[0142] The effect of TrpRS on bone marrow--derived macrophage
activity was investigated. Alexa 647 labeled full-length TrpRS
(FL-WRS) or mini-TrpRS (mini-WRS) were inoculated into the ear of
mice and photographed 1 and 4 hours post-infection using in vivo
imaging techniques. In addition, S. typhimurium labeled with Alexa
647 combined with Full length-TrpRS or mini-TrpRS was inoculated
into the ear of GFP-LysM Tg mice capable of observing neutrophils
and macrophages by GFP expression. To observe macrophages in mice,
macrophages were photographed using in vivo imaging technology and
counted. Immuno-cellular dynamics were visualized using a
custom-built video-rate laser-scanning confocal microscope imaging
system (Choe et al., 2013; Seo et al., 2015). Three consecutive
lasers were used as the fluorescent stimulus source. Three
fluorescence colors emitted from the mice were detected as highly
sensitive optoelectronic layer tubes at 488 nm (MLD, Cobolt), 561
nm (Jive, Cobolt) and 640 nm (MLD, Cobolt). And it was digitized by
the 8-bit 3-channel frame grabber.
[0143] As a result, it was confirmed that infiltration of
neutrophils and macrophages appeared at the site of full-length
TrpRS inoculation instead of mini-TrpRS. Such an infiltration
started at 1 hour after inoculation, and the amount of infiltration
at 4 hours after inoculation was the highest (FIG. 15A). In
addition, it was confirmed that phagocytic index of macrophage was
increased in mice treated with full length-TrpRS (FL-WRS) as
compared to mice treated with mini-TrpRS (mini-WRS) or PBS(Con)
(FIG. 15B).
Example 4
TrpRS Inhibition-Devised Effect
Example 4-1. Preparation of Antibodies Specifically Binding to
TrpRS
[0144] TrpRS was titrated with TrpRS-specific antibodies to further
validate the protective role of TrpRS against infection. First, an
antibody that specifically binds N154 peptide of human TrpRS was
prepared by panning a library of phage display human single chain
variable fragments (scFV) (FIG. 16) Immuno tubes were coated with
TrpRS 10 and blocked with MPBS (PBS with 3% nonfat dried milk).
Phage-displayed scFv library (1.times.10.sup.13 CFU) was added to 1
ml of mPBST, added to the immune tube, incubated for 2 hours and
then washed 3-5 times with PB ST. The bound phage was eluted with 1
mL of 100 mM trimethylamine and neutralized with 0.5 mL of 1 M
Tris-HCl (pH 7.0). E. coli ER257 was infected with the eluted phage
and cultured in LB medium containing 2% glucose and ampicillin for
one day, and bacteria were collected from the medium logarithm. The
bacteria were then cultured in 20 mL SB (3% Tryptone, 2% yeast
extract, 1% MOPS, pH 7.0) supplemented with ampicillin to an OD600
of 0.5. VCSM13 helper phage (1.times.10.sup.11 PFU) was added and
incubated at 37.degree. C. for 1 hour, followed by kanamycin (70
.mu.g/ml) and incubated overnight at 30.degree. C. The supernatant
was removed by centrifugation, and phage precipitation solution (4%
PEG 8000 and 3% NaCl, final concentration) was added and mixed.
After 30 minutes of incubation on ice, the precipitated phage were
collected by centrifugation. After panning the library four times,
individual scFv clones capable of binding TrpRS were screened. This
process is illustrated in FIG. 16.
[0145] In order to confirm whether the prepared antibodies
specifically bound to TrpRS affects the effect of TrpRS on
infection, the following experiment was conducted.
[0146] PBMC was treated with the prepared antibody (10 .mu.g/mL)
and infected with S. typhimurium (MOI=1) as described in Example 1
above. The secretion pattern of TNF-.alpha. in cell culture was
measured by ELISA. In order to confirm whether scFv 4G1 binds to
full length-TrpRS (FL-WRS) by selecting 4G1 clones, PBMC cell
lysates were extracted and immunoblotted.
[0147] As a result, it was confirmed that the F9, Ell, and 4G1
clones among some clones showed a decrease in the secretion amount
of TNF-.alpha. of full length-TrpRS in human PBMC cells (FIG. 17A),
while both only 4G1 treatment and full length-TrpRS and 4G1
treatment (FIG. 17B) decreased the amount of the secreted
TNF-.alpha.. In addition, it was confirmed through immunoblotting
that scFV 4G1 specifically binds to full length-TrpRS (FIG.
17C).
Example 4-2. Decreased Secretion of TNF-.alpha. and MIP1-.alpha. by
TrpRS-Specific Antibodies
[0148] To examine the effect of the scFV 4G1 prepared in Example
5-1 on the innate immune response in the body, an animal experiment
using mice was carried out according to the experimental outline of
FIG. 18A.
[0149] Mice were injected with PBS or scFv 4G1 in infected or
uninfected groups by intraperitoneal injection of S. typhimurium.
Four hours after the infection, the peritoneal fluid was extracted,
and the number of Ly6G.sup.+ cells was measured by flow cytometry.
The amount of MIP-1.alpha. and TNF-.alpha. was analyzed by ELISA.
The statistical significance of the comparison between the
PBS-treated negative control and the results of each experimental
condition was verified by one-way Anova test using GraphPad (ver.
4.0) software.***p<0.001, **p<0.01
[0150] ELISA analysis showed that the amount of MIP-1 alpha and
TNF-.alpha. decreased in scFv 4G1-treated mice (FIG. 18B). In
addition, flow cytometry analysis showed that Ly6G.sup.+
macrophages decreased in scFv 4G1-treated mice (FIG. 18C).
Example 4-3. Effect of TrpRS-Specific Antibodies on Survival of
Bacterially Infected Mice
[0151] To confirm the effect of the scFv 4G1 prepared in Example
5-1 on the survival rate of the mice, an animal experiment using a
mouse was conducted according to the experimental outline of FIG.
18A, and survival analysis was performed. As described above, mice
were injected with PBS or scFv 4G1 in infected or uninfected groups
by injecting S. typhimurium into the abdominal cavity. The survival
rate of mice was 12, 24, 36, 48 hours after infection.
[0152] As a result, in the control, ST+PBS (injection of PBS after
infection with S. typhimurium) survival rate was 50% at 24 hours
and 25% at 48 hours, but in ST+4G1 (scFv 4G1 injection after S.
typhimurium infection) survival rate was less than 25%, and 0% at
36 hours. Thus, it was confirmed that the survival rate of mice was
decreased in the group injected with scFv 4G1 (FIG. 19).
Example 5
Effect of TrpRS In Vivo Infection Inhibition and Increased Survival
Rate after Infection
Example 5-1. Effect of TrpRS on the Absorption of Infecting
Bacteria by Invasive Neutrophils
[0153] To investigate the effect of TrpRS on the survival rate of
mice infected with S. typhimurium, an animal experiment using mice
was carried out according to the outline of the experiment of FIG.
20 (FIG. 20, top), and the amount of S. typhimurium absorbed by and
adsorbed onto infiltrated neutrophil was confirmed for one hour
after infection (FIG. 20, bottom).
[0154] PBS or TrpRS (10 .mu.g, 0.5 mg/kg) was injected
intraperitoneally into mice (C57BL/6 mouse, 9-12 week old female)
and fluorescently labeled S. typhimurium (FITC-labeled S.
Typhimurium, 1.times.10.sup.7 CFU/mouse, 5.about.6 per group) was
injected into the abdominal cavity 1 hour later. One hour after
infection, mice were sacrificed and the peritoneal cells were
separated and stained with Ly6G, Ly6C antibody and analyzed by flow
cytometry. Statistical significance was verified by t-test.
***p<0.001
[0155] As a result, it was confirmed that the number of
infiltrating neutrophils (Ly6G.sup.+ Neutrophils) was also
significantly increased in the full-length TrpRS-treated group
(TrpRS-Full) compared with the PBS-treated control group (PBS), and
that S. typhimurium (FITC-S. typhimurium+/Ly6G.sup.+ neutrophil)
adsorbed onto and absorbed by neutrophils was significantly
increased.
Example 5-2. Effects of TrpRS on Bacterial Clearance in Spleen and
Liver
[0156] An animal experiment using a mouse was performed according
to the outline of FIG. 15, and the degree of bacterial clearance of
the spleen after 4 hours of infection was observed (FIG. 21). After
4 hours of infection with S. typhimurim (FIG. 21A) or L.
monocytogenes (FIG. 21B), mice were sacrificed. Spleen and hepatic
homogenate were made and cultured in NB agar medium (serial ratios
of 4 to 8 mice per group) by 10.times. serial dilution. After
culturing at 37.degree. C. for 24 hours, the bacterial CFU was
calculated and analyzed. Statistical significance was then verified
by t-test using GraphPad (ver. 4.0) software. **p<0.01
[0157] As a result, it was confirmed that, in S.
typhimurium-infected mice, bacterial CFU in the spleen and liver of
the group treated with full-length TrpRS was significantly reduced,
compared with the group treated with mini-TrpRS (mini-WRS) or PBS
(FIG. 21A). In mice infected with L. monocytogenes, the bacterial
CFU in the spleen and liver of the group treated with full
length-TrpRS (FL-WRS) was significantly lower than that of the
group treated with mini-TrpRS (mini-WRS) (FIG. 21B). This shows
that in the spleen and liver of TrpRS treated mice, the bacteria
were eliminated before they caused cell infections.
Example 5-3. Effect of TrpRS on the Survival Rate of
Bacteria-Infected Mice
[0158] To investigate the effect of TrpRS on the survival rate of
mice infected with S. typhimurim (FIG. 22A) or L. monocytogenes
(FIG. 22B), animal experiments with mice were carried out according
to the experimental outline of FIG. 21 (FIG. 22). Mice were
injected with PBS, full-length TrpRS (FL-WRS) or mini-TrpRS
(mini-WRS), followed by infusion of 1.times.10.sup.7 CFU S.
typhimurium or L. monocytogenes into the peritoneal cavity. The
survival rate of the mice at 12, 24, 36 and 48 hours after the
infection was expressed as a survival plot according to the
treatment conditions.
[0159] As a result, S. typhimurim-infected mice that were given
full length-TrpRS were 100% viable until 36 hours post-infection
and 75% survived until 48 hours post-infection, whereas the mice
receiving PBS or mini-TrpRS were found to have over 80% mortality
at 48 hours post-infection (FIG. 22A). L. monocytogenes-infected
mice that received full length-TrpRS also survived 100% until 48 h
before infection and 75% survived at 48 h after infection, whereas
75% of the mice receiving PBS or mini-TrpRS died in 24 hours (FIG.
22B). This indicates that the survival time of the TrpRS injected
group was significantly longer than that of the control group or
the mini-TrpRS treated group by the single injection of TrpRS
alone.
[0160] The results of the above Examples show that full-length
TrpRS lowers the mortality of bacteria-infected mice by activating
innate immune responses.
INDUSTRIAL AVAILABILITY
[0161] As described above, the composition of the present invention
can be effectively used to prevent diseases of humans and animals
caused by bacterial, viral or fungal infection by inhibiting
bacterial, viral or fungal infection at an early stage,
particularly through activating innate immune response. In
addition, the composition of the present invention can be used for
immune enhancement and is highly industrially applicable.
Sequence CWU 1
1
181471PRTHomo sapiensNP_004175.2, NCBI Gene Database 1Met Pro Asn
Ser Glu Pro Ala Ser Leu Leu Glu Leu Phe Asn Ser Ile1 5 10 15Ala Thr
Gln Gly Glu Leu Val Arg Ser Leu Lys Ala Gly Asn Ala Ser 20 25 30Lys
Asp Glu Ile Asp Ser Ala Val Lys Met Leu Val Ser Leu Lys Met 35 40
45Ser Tyr Lys Ala Ala Ala Gly Glu Asp Tyr Lys Ala Asp Cys Pro Pro
50 55 60Gly Asn Pro Ala Pro Thr Ser Asn His Gly Pro Asp Ala Thr Glu
Ala65 70 75 80Glu Glu Asp Phe Val Asp Pro Trp Thr Val Gln Thr Ser
Ser Ala Lys 85 90 95Gly Ile Asp Tyr Asp Lys Leu Ile Val Arg Phe Gly
Ser Ser Lys Ile 100 105 110Asp Lys Glu Leu Ile Asn Arg Ile Glu Arg
Ala Thr Gly Gln Arg Pro 115 120 125His His Phe Leu Arg Arg Gly Ile
Phe Phe Ser His Arg Asp Met Asn 130 135 140Gln Val Leu Asp Ala Tyr
Glu Asn Lys Lys Pro Phe Tyr Leu Tyr Thr145 150 155 160Gly Arg Gly
Pro Ser Ser Glu Ala Met His Val Gly His Leu Ile Pro 165 170 175Phe
Ile Phe Thr Lys Trp Leu Gln Asp Val Phe Asn Val Pro Leu Val 180 185
190Ile Gln Met Thr Asp Asp Glu Lys Tyr Leu Trp Lys Asp Leu Thr Leu
195 200 205Asp Gln Ala Tyr Ser Tyr Ala Val Glu Asn Ala Lys Asp Ile
Ile Ala 210 215 220Cys Gly Phe Asp Ile Asn Lys Thr Phe Ile Phe Ser
Asp Leu Asp Tyr225 230 235 240Met Gly Met Ser Ser Gly Phe Tyr Lys
Asn Val Val Lys Ile Gln Lys 245 250 255His Val Thr Phe Asn Gln Val
Lys Gly Ile Phe Gly Phe Thr Asp Ser 260 265 270Asp Cys Ile Gly Lys
Ile Ser Phe Pro Ala Ile Gln Ala Ala Pro Ser 275 280 285Phe Ser Asn
Ser Phe Pro Gln Ile Phe Arg Asp Arg Thr Asp Ile Gln 290 295 300Cys
Leu Ile Pro Cys Ala Ile Asp Gln Asp Pro Tyr Phe Arg Met Thr305 310
315 320Arg Asp Val Ala Pro Arg Ile Gly Tyr Pro Lys Pro Ala Leu Leu
His 325 330 335Ser Thr Phe Phe Pro Ala Leu Gln Gly Ala Gln Thr Lys
Met Ser Ala 340 345 350Ser Asp Pro Asn Ser Ser Ile Phe Leu Thr Asp
Thr Ala Lys Gln Ile 355 360 365Lys Thr Lys Val Asn Lys His Ala Phe
Ser Gly Gly Arg Asp Thr Ile 370 375 380Glu Glu His Arg Gln Phe Gly
Gly Asn Cys Asp Val Asp Val Ser Phe385 390 395 400Met Tyr Leu Thr
Phe Phe Leu Glu Asp Asp Asp Lys Leu Glu Gln Ile 405 410 415Arg Lys
Asp Tyr Thr Ser Gly Ala Met Leu Thr Gly Glu Leu Lys Lys 420 425
430Ala Leu Ile Glu Val Leu Gln Pro Leu Ile Ala Glu His Gln Ala Arg
435 440 445Arg Lys Glu Val Thr Asp Glu Ile Val Lys Glu Phe Met Thr
Pro Arg 450 455 460Lys Leu Ser Phe Asp Phe Gln465 4702481PRTRattus
norvegicusQ6P7B0.2, NCBI Gene Database 2Met Ala Asp Met Pro Ser Gly
Glu Ser Cys Thr Ser Pro Leu Glu Leu1 5 10 15Phe Asn Ser Ile Ala Ala
Gln Gly Glu Leu Val Arg Ser Leu Lys Ala 20 25 30Gly Asn Ala Pro Lys
Asp Glu Ile Glu Ser Ala Val Lys Met Leu Leu 35 40 45Ser Leu Lys Met
Asn Tyr Lys Thr Ala Met Gly Glu Glu Tyr Lys Ala 50 55 60Gly Cys Pro
Pro Gly Asn Ser Thr Ala Gly Ser Asn Gly Asp Pro Asp65 70 75 80Ala
Thr Lys Ala Ser Glu Asp Phe Val Asp Pro Trp Thr Val Arg Thr 85 90
95Ser Ser Ala Lys Gly Ile Asp Tyr Asp Lys Leu Ile Val Gln Phe Gly
100 105 110Ser Ser Lys Ile Asp Lys Glu Leu Ile Asn Arg Ile Glu Arg
Ala Thr 115 120 125Gly Gln Arg Pro His Arg Phe Leu Arg Arg Gly Ile
Phe Phe Ser His 130 135 140Arg Asp Met Asn Gln Ile Leu Asp Ala Tyr
Glu Asn Lys Lys Pro Phe145 150 155 160Tyr Leu Tyr Thr Gly Arg Gly
Pro Ser Ser Glu Ala Met His Leu Gly 165 170 175His Leu Val Pro Phe
Ile Phe Thr Lys Trp Leu Gln Asp Val Phe Asp 180 185 190Val Pro Leu
Val Ile Gln Met Ser Asp Asp Glu Lys Tyr Leu Trp Lys 195 200 205Asp
Leu Thr Leu Glu Gln Ala Tyr Ser Tyr Thr Val Glu Asn Ala Lys 210 215
220Asp Ile Ile Ala Cys Gly Phe Asp Val Asn Lys Thr Phe Ile Phe
Ser225 230 235 240Asp Leu Glu Tyr Met Gly Gln Ser Pro Gly Phe Tyr
Lys Asn Val Val 245 250 255Lys Ile Gln Lys His Val Thr Phe Asn Gln
Val Lys Gly Ile Phe Gly 260 265 270Phe Thr Asp Ser Asp Cys Ile Gly
Lys Ile Ser Phe Pro Ala Val Gln 275 280 285Ala Ala Pro Ser Phe Ser
Asn Ser Phe Pro Lys Ile Phe Arg Asp Arg 290 295 300Thr Asp Ile Gln
Cys Leu Ile Pro Cys Ala Ile Asp Gln Asp Pro Tyr305 310 315 320Phe
Arg Met Thr Arg Asp Val Ala Pro Arg Ile Gly His Pro Lys Pro 325 330
335Ala Leu Leu His Ser Thr Phe Phe Pro Ala Leu Gln Gly Ala Gln Thr
340 345 350Lys Met Ser Ala Ser Asp Pro Asn Ser Ser Ile Phe Leu Thr
Asp Thr 355 360 365Ala Lys Gln Ile Lys Ser Lys Val Asn Lys His Ala
Phe Ser Gly Gly 370 375 380Arg Asp Thr Val Glu Glu His Arg Gln Phe
Gly Gly Asn Cys Glu Val385 390 395 400Asp Val Ser Phe Met Tyr Leu
Thr Phe Phe Leu Glu Asp Asp Asp Ser 405 410 415Leu Glu Gln Ile Arg
Lys Asp Tyr Thr Ser Gly Ala Met Leu Thr Gly 420 425 430Glu Leu Lys
Lys Thr Leu Ile Asp Val Leu Gln Pro Leu Ile Ala Glu 435 440 445His
Gln Ala Arg Arg Lys Ala Val Thr Glu Glu Thr Val Lys Glu Phe 450 455
460Met Ala Pro Arg Gln Leu Ser Phe His Phe Gln Cys Phe Cys Phe
Asp465 470 475 480Thr3481PRTMus musculusP32921.2, NCBI Gene
Database 3Met Ala Asp Met Pro Ser Gly Glu Ser Cys Thr Ser Pro Leu
Glu Leu1 5 10 15Phe Asn Ser Ile Ala Thr Gln Gly Glu Leu Val Arg Ser
Leu Lys Ala 20 25 30Gly Asn Ala Pro Lys Asp Glu Ile Asp Ser Ala Val
Lys Met Leu Leu 35 40 45Ser Leu Lys Met Ser Tyr Lys Ala Ala Met Gly
Glu Glu Tyr Lys Ala 50 55 60Gly Cys Pro Pro Gly Asn Pro Thr Ala Gly
Arg Asn Cys Asp Ser Asp65 70 75 80Ala Thr Lys Ala Ser Glu Asp Phe
Val Asp Pro Trp Thr Val Arg Thr 85 90 95Ser Ser Ala Lys Gly Ile Asp
Tyr Asp Lys Leu Ile Val Gln Phe Gly 100 105 110Ser Ser Lys Ile Asp
Lys Glu Leu Ile Asn Arg Ile Glu Arg Ala Thr 115 120 125Gly Gln Arg
Pro His Arg Phe Leu Arg Arg Gly Ile Phe Phe Ser His 130 135 140Arg
Asp Met Asn Gln Ile Leu Asp Ala Tyr Glu Asn Lys Lys Pro Phe145 150
155 160Tyr Leu Tyr Thr Gly Arg Gly Pro Ser Ser Glu Ala Met His Leu
Gly 165 170 175His Leu Val Pro Phe Ile Phe Thr Lys Trp Leu Gln Asp
Val Phe Asn 180 185 190Val Pro Leu Val Ile Gln Met Ser Asp Asp Glu
Lys Tyr Leu Trp Lys 195 200 205Asp Leu Thr Leu Glu Gln Ala Tyr Ser
Tyr Thr Val Glu Asn Ala Lys 210 215 220Asp Ile Ile Ala Cys Gly Phe
Asp Ile Asn Lys Thr Phe Ile Phe Ser225 230 235 240Asp Leu Glu Tyr
Met Gly Gln Ser Pro Gly Phe Tyr Arg Asn Val Val 245 250 255Lys Ile
Gln Lys His Val Thr Phe Asn Gln Val Lys Gly Ile Phe Gly 260 265
270Phe Thr Asp Ser Asp Cys Ile Gly Lys Ile Ser Phe Pro Ala Val Gln
275 280 285Ala Ala Pro Ser Phe Ser Asn Ser Phe Pro Lys Ile Phe Arg
Asp Arg 290 295 300Thr Asp Ile Gln Cys Leu Ile Pro Cys Ala Ile Asp
Gln Asp Pro Tyr305 310 315 320Phe Arg Met Thr Arg Asp Val Ala Pro
Arg Ile Gly His Pro Lys Pro 325 330 335Ala Leu Leu His Ser Thr Phe
Phe Pro Ala Leu Gln Gly Ala Gln Thr 340 345 350Lys Met Ser Ala Ser
Asp Pro Asn Ser Ser Ile Phe Leu Thr Asp Thr 355 360 365Ala Lys Gln
Ile Lys Ser Lys Val Asn Lys His Ala Phe Ser Gly Gly 370 375 380Arg
Asp Thr Val Glu Glu His Arg Gln Phe Gly Gly Asn Cys Glu Val385 390
395 400Asp Val Ser Phe Met Tyr Leu Thr Phe Phe Leu Glu Asp Asp Asp
Arg 405 410 415Leu Glu Gln Ile Arg Lys Asp Tyr Thr Ser Gly Ala Met
Leu Thr Gly 420 425 430Glu Leu Lys Lys Thr Leu Ile Asp Val Leu Gln
Pro Leu Ile Ala Glu 435 440 445His Gln Ala Arg Arg Lys Ala Val Thr
Glu Glu Thr Val Lys Glu Phe 450 455 460Met Thr Pro Arg Gln Leu Ser
Phe His Phe Gln Cys Phe Cys Phe Asp465 470 475 480Thr4476PRTBos
taurusP17248.3, NCBI Gene Database 4Met Ala Asp Met Ser Asn Gly Glu
Gln Gly Cys Gly Ser Pro Leu Glu1 5 10 15Leu Phe His Ser Ile Ala Ala
Gln Gly Glu Leu Val Arg Asp Leu Lys 20 25 30Ala Arg Asn Ala Ala Lys
Asp Glu Ile Asp Ser Ala Val Lys Met Leu 35 40 45Leu Ser Leu Lys Thr
Ser Tyr Lys Ala Ala Thr Gly Glu Asp Tyr Lys 50 55 60Val Asp Cys Pro
Pro Gly Asp Pro Ala Pro Glu Ser Gly Glu Gly Leu65 70 75 80Asp Ala
Thr Glu Ala Asp Glu Asp Phe Val Asp Pro Trp Thr Val Gln 85 90 95Thr
Ser Ser Ala Lys Gly Ile Asp Tyr Asp Lys Leu Ile Val Arg Phe 100 105
110Gly Ser Ser Lys Ile Asp Lys Glu Leu Val Asn Arg Ile Glu Arg Ala
115 120 125Thr Gly Gln Arg Pro His Arg Phe Leu Arg Arg Gly Ile Phe
Phe Ser 130 135 140His Arg Asp Met His Gln Ile Leu Asp Ala Tyr Glu
Asn Lys Lys Pro145 150 155 160Phe Tyr Leu Tyr Thr Gly Arg Gly Pro
Ser Ser Glu Ala Met His Val 165 170 175Gly His Leu Ile Pro Phe Ile
Phe Thr Lys Trp Leu Gln Asp Val Phe 180 185 190Asn Val Pro Leu Val
Ile Gln Met Thr Asp Asp Glu Lys Tyr Leu Trp 195 200 205Lys Asp Leu
Thr Leu Asp Gln Ala Tyr Gly Tyr Ala Val Glu Asn Ala 210 215 220Lys
Asp Ile Ile Ala Cys Gly Phe Asp Ile Asn Lys Thr Phe Ile Phe225 230
235 240Ser Asp Leu Asp Tyr Met Gly Met Ser Pro Gly Phe Tyr Lys Asn
Val 245 250 255Val Lys Ile Gln Lys His Val Thr Phe Asn Gln Val Lys
Gly Ile Phe 260 265 270Gly Phe Thr Asp Ser Asp Cys Ile Gly Lys Ile
Ser Phe Pro Ala Ile 275 280 285Gln Ala Ala Pro Ser Phe Ser Asn Ser
Phe Pro Gln Ile Phe Arg Asp 290 295 300Arg Thr Asp Val Gln Cys Leu
Ile Pro Cys Ala Ile Asp Gln Asp Pro305 310 315 320Tyr Phe Arg Met
Thr Arg Asp Val Ala Pro Arg Ile Gly Tyr Pro Lys 325 330 335Pro Ala
Leu Leu His Ser Thr Phe Phe Pro Ala Leu Gln Gly Ala Gln 340 345
350Thr Lys Met Ser Ala Ser Asp Pro Asn Ser Ser Ile Phe Leu Thr Asp
355 360 365Thr Ala Lys Gln Ile Lys Thr Lys Val Asn Lys His Ala Phe
Ser Gly 370 375 380Gly Arg Asp Thr Val Glu Glu His Arg Gln Phe Gly
Gly Asn Cys Asp385 390 395 400Val Asp Val Ser Phe Met Tyr Leu Thr
Phe Phe Leu Glu Asp Asp Asp 405 410 415Lys Leu Glu Gln Ile Arg Arg
Asp Tyr Thr Ser Gly Ala Met Leu Thr 420 425 430Gly Glu Leu Lys Lys
Glu Leu Ile Glu Val Leu Gln Pro Leu Ile Ala 435 440 445Glu His Gln
Ala Arg Arg Lys Glu Val Thr Asp Glu Ile Val Lys Glu 450 455 460Phe
Met Thr Pro Arg Lys Leu Ser Tyr Asp Phe Gln465 470 4755476PRTSus
scrofaJAA53775.1, NCBI Gene Database 5Met Ala Asp Val Pro Asn Gly
Glu Gln Gly Cys Ser Ser Pro Leu Glu1 5 10 15Leu Phe Asn Ser Ile Ala
Ala Gln Gly Glu Leu Val Arg Ser Leu Lys 20 25 30Ala Arg His Ala Ala
Lys Asp Glu Ile Asp Ser Ala Val Lys Met Leu 35 40 45Leu Ser Leu Lys
Met Ser Tyr Lys Ala Ala Met Gly Glu Asp Tyr Lys 50 55 60Ala Asp Cys
Pro Pro Gly Asn Arg Ala Pro Gly Ile Asp Ser Gly Leu65 70 75 80Asp
Ala Thr Glu Ala Gly Asp Asp Phe Val Asp Pro Trp Thr Val Gln 85 90
95Thr Ser Ser Ala Lys Gly Ile Asp Tyr Asp Lys Leu Ile Val Arg Phe
100 105 110Gly Ser Ser Lys Ile Asp Lys Glu Leu Ile Asp Arg Ile Glu
Arg Ala 115 120 125Thr Gly Gln Arg Pro His Arg Phe Leu Arg Arg Gly
Ile Phe Phe Ser 130 135 140His Arg Asp Met Asn Gln Val Leu Asp Ala
Tyr Glu Asn Lys Lys Pro145 150 155 160Phe Tyr Leu Tyr Thr Gly Arg
Gly Pro Ser Ser Glu Ala Met His Val 165 170 175Gly His Leu Ile Pro
Phe Ile Phe Thr Lys Trp Leu Gln Asp Val Phe 180 185 190Asn Val Pro
Leu Val Ile Gln Met Thr Asp Asp Glu Lys Tyr Leu Trp 195 200 205Lys
Glu Leu Thr Leu Glu Gln Ala His Gly Tyr Ala Val Glu Asn Ala 210 215
220Lys Asp Ile Ile Ala Cys Gly Phe Asp Val Asn Lys Thr Phe Ile
Phe225 230 235 240Ser Asp Leu Asp Tyr Met Gly Met Ser Pro Gly Phe
Tyr Lys Asn Val 245 250 255Val Lys Ile Gln Lys His Val Thr Phe Asn
Gln Val Lys Gly Ile Phe 260 265 270Gly Phe Thr Asp Ser Asp Cys Ile
Gly Lys Ile Ser Phe Pro Ala Ile 275 280 285Gln Ala Ala Pro Ser Phe
Ser Ser Ser Phe Pro Gln Ile Phe Arg Asp 290 295 300Arg Thr Asp Ile
Gln Cys Leu Ile Pro Cys Ala Ile Asp Gln Asp Pro305 310 315 320Tyr
Phe Arg Met Thr Arg Asp Val Ala Pro Arg Ile Gly Tyr Pro Lys 325 330
335Pro Ala Leu Leu His Ser Thr Phe Phe Pro Ala Leu Gln Gly Ala Gln
340 345 350Thr Lys Met Ser Ala Ser Asp Pro Asn Ser Ser Ile Phe Leu
Thr Asp 355 360 365Thr Ala Lys Gln Ile Lys Thr Lys Val Asn Lys His
Ala Phe Ser Gly 370 375 380Gly Arg Asp Thr Ile Glu Glu His Arg Gln
Phe Gly Gly Asn Cys Asp385 390 395 400Val Asp Val Ser Phe Met Tyr
Leu Thr Phe Phe Leu Glu Asp Asp Asp 405 410 415Arg Leu Glu Gln Ile
Arg Lys Asp Tyr Ser Ser Gly Ala Met Leu Thr 420 425 430Gly Glu Leu
Lys Lys Val Leu Ile Glu Val Leu Gln Pro Leu Ile Ala 435 440 445Glu
His Gln Ala Arg Arg Lys Glu Val Thr Asp Glu Val Val Lys Glu 450 455
460Phe Met Thr Pro Arg Lys Leu Ser Tyr Asp Phe Glu465 470
4756476PRTOvis ariesXP_004018038.1, NCBI Gene Database 6Met Ala Asp
Met Pro Asn Gly Glu Gln Gly Tyr Gly Ser Pro Leu Glu1 5 10 15Leu Phe
His Ser Ile Ala Ala Gln Gly Glu Leu Val Arg Gly Leu Lys 20 25 30Ala
Arg Asn Ala Ala Lys Asp Glu Ile Asp Ser Ala Val Lys Met Leu 35 40
45Leu Ser Leu Lys Thr Ser Tyr Lys Ala Ala Thr
Gly Glu Asp Tyr Lys 50 55 60Gly Asp His Pro Pro Glu Asp Pro Ala Pro
Glu Ser Gly Glu Gly Leu65 70 75 80Asp Ala Thr Gly Ala Asp Glu Asp
Phe Val Asp Pro Trp Thr Val Gln 85 90 95Thr Ser Ser Ala Lys Gly Ile
Asp Tyr Asp Lys Leu Ile Val Arg Phe 100 105 110Gly Ser Ser Lys Ile
Asp Lys Glu Leu Val Asn Arg Ile Glu Arg Ala 115 120 125Thr Gly Gln
Arg Pro His Arg Phe Leu Arg Arg Gly Ile Phe Phe Ser 130 135 140His
Arg Asp Met His Gln Ile Leu Asp Ala Tyr Glu Asn Lys Lys Pro145 150
155 160Phe Tyr Leu Tyr Thr Gly Arg Gly Pro Ser Ser Glu Ala Met His
Val 165 170 175Gly His Leu Ile Pro Phe Ile Phe Thr Lys Trp Leu Gln
Asp Val Phe 180 185 190Asn Val Pro Leu Val Ile Gln Met Thr Asp Asp
Glu Lys Tyr Leu Trp 195 200 205Lys Asp Leu Thr Leu Asp Gln Ala Tyr
Gly Tyr Ala Val Glu Asn Ala 210 215 220Lys Asp Ile Ile Ala Cys Gly
Phe Asp Ile Asn Lys Thr Phe Ile Phe225 230 235 240Ser Asp Leu Asp
Tyr Met Gly Met Ser Pro Gly Phe Tyr Lys Asn Val 245 250 255Val Lys
Ile Gln Lys His Val Thr Phe Asn Gln Val Lys Gly Ile Phe 260 265
270Gly Phe Thr Asp Ser Asp Cys Ile Gly Lys Ile Ser Phe Pro Ala Ile
275 280 285Gln Ala Ala Pro Ser Phe Ser Asn Ser Phe Pro Gln Ile Phe
Arg Asp 290 295 300Arg Thr Asp Val Gln Cys Leu Ile Pro Cys Ala Ile
Asp Gln Asp Pro305 310 315 320Tyr Phe Arg Met Thr Arg Asp Val Ala
Pro Arg Ile Gly Tyr Pro Lys 325 330 335Pro Ala Leu Leu His Ser Thr
Phe Phe Pro Ala Leu Gln Gly Ala Gln 340 345 350Thr Lys Met Ser Ala
Ser Asp Pro Asn Ser Ser Ile Phe Leu Thr Asp 355 360 365Thr Ala Lys
Gln Ile Lys Thr Lys Val Asn Lys His Ala Phe Ser Gly 370 375 380Gly
Arg Asp Thr Ile Glu Glu His Arg Gln Leu Gly Gly Asn Cys Asp385 390
395 400Val Asp Val Ser Phe Met Tyr Leu Thr Phe Phe Leu Glu Asp Asp
Asp 405 410 415Arg Leu Glu Gln Ile Arg Lys Asp Tyr Thr Ser Gly Ala
Met Leu Thr 420 425 430Gly Glu Leu Lys Lys Glu Leu Ile Glu Val Leu
Gln Pro Leu Ile Ala 435 440 445Glu His Gln Ala Arg Arg Lys Glu Val
Thr Asp Glu Ile Val Lys Glu 450 455 460Phe Met Thr Pro Arg Lys Leu
Ser Tyr Asp Phe Gln465 470 4757476PRTCanis lupusXP_537554.1, NCBI
Gene Database 7Met Ala Asp Met Pro Asn Gly Glu Gln Gly Phe Ala Ser
Pro Leu Glu1 5 10 15Leu Phe Asn Ser Ile Ala Ala Gln Gly Glu Leu Val
Arg Ser Leu Lys 20 25 30Ala Gly Lys Ala Ser Lys Asp Glu Ile Asp Ser
Ala Val Lys Leu Leu 35 40 45Leu Ser Leu Lys Met Ser Tyr Lys Ala Thr
Val Gly Glu Glu Tyr Lys 50 55 60Ala Asp Cys Pro Pro Ala Arg Pro Ala
Pro Glu Asn Ser Arg Gly Leu65 70 75 80Asn Ala Ala Glu Ala Glu Glu
Asp Phe Val Asp Pro Trp Thr Val Gln 85 90 95Thr Ser Ser Ala Lys Gly
Ile Asp Tyr Asp Lys Leu Ile Val Arg Phe 100 105 110Gly Ser Ser Lys
Ile Asp Lys Glu Leu Val Asn Arg Ile Glu Arg Ala 115 120 125Thr Gly
Gln Lys Pro His Arg Phe Leu Arg Arg Gly Ile Phe Phe Ser 130 135
140His Arg Asp Met Asn Gln Ile Leu Asp Ala Tyr Glu Asn Lys Lys
Pro145 150 155 160Phe Tyr Leu Tyr Thr Gly Arg Gly Pro Ser Ser Glu
Ala Met His Val 165 170 175Gly His Leu Ile Pro Phe Ile Phe Thr Lys
Trp Leu Gln Asp Val Phe 180 185 190Asn Val Pro Leu Val Ile Gln Met
Thr Asp Asp Glu Lys Tyr Leu Trp 195 200 205Lys Asp Leu Thr Leu Asp
Gln Ala Tyr Gly Tyr Ala Val Glu Asn Ala 210 215 220Lys Asp Ile Ile
Ala Cys Gly Phe Asp Ile Lys Lys Thr Phe Ile Phe225 230 235 240Ser
Asp Leu Asp Tyr Met Gly Met Ser Pro Gly Phe Tyr Lys Asn Val 245 250
255Val Lys Ile Gln Lys His Val Thr Phe Asn Gln Val Lys Gly Ile Phe
260 265 270Gly Phe Thr Asp Ser Asp Ser Ile Gly Lys Ile Ser Phe Pro
Ala Ile 275 280 285Gln Ala Ala Pro Ser Phe Ser Asn Ser Phe Pro Gln
Ile Phe Arg Asp 290 295 300Arg Thr Asp Ile Gln Cys Leu Ile Pro Cys
Ala Ile Asp Gln Asp Pro305 310 315 320Tyr Phe Arg Met Thr Arg Asp
Val Ala Pro Arg Ile Gly Tyr Pro Lys 325 330 335Pro Ala Leu Leu His
Ser Thr Phe Phe Pro Ala Leu Gln Gly Ala Gln 340 345 350Thr Lys Met
Ser Ala Ser Asp Pro Asn Ser Ser Ile Phe Leu Thr Asp 355 360 365Thr
Ala Lys Gln Ile Lys Thr Lys Val Asn Lys His Ala Phe Ser Gly 370 375
380Gly Arg Asp Thr Ile Glu Glu His Arg Gln Phe Gly Gly Asn Cys
Asp385 390 395 400Val Asp Val Ser Phe Met Tyr Leu Thr Phe Phe Leu
Glu Asp Asp Asp 405 410 415Lys Leu Glu Gln Ile Arg Lys Asp Tyr Thr
Ser Gly Asp Met Leu Thr 420 425 430Gly Glu Leu Lys Lys Thr Leu Ile
Glu Val Leu Gln Pro Leu Ile Ala 435 440 445Glu His Gln Ala Arg Arg
Lys Glu Val Thr Asp Glu Ile Val Lys Glu 450 455 460Phe Met Thr Pro
Arg Lys Leu Ser Tyr Asp Phe Gln465 470 4758476PRTFelis
catusXP_003988038.1, NCBI Gene Database 8Met Ala Asp Val Pro Asn
Gly Glu Gln Gly Cys Ala Ser Pro Leu Glu1 5 10 15Leu Phe Asn Arg Ile
Ala Ala Gln Gly Glu Leu Val Arg Ser Leu Lys 20 25 30Ala Gly Lys Ala
Pro Gln Asp Glu Ile Asp Ser Ala Val Gln Met Leu 35 40 45Leu Ser Leu
Lys Met Ser Tyr Lys Ala Ala Met Gly Glu Asp Tyr Lys 50 55 60Ala Asp
Cys Pro Pro Gly Asn Pro Ala Pro Gly Asn Asn Ser Gly Leu65 70 75
80Gly Ala Thr Glu Ala Glu Glu Asp Phe Val Asp Pro Trp Thr Val Gln
85 90 95Thr Ser Ser Ala Lys Gly Ile Asp Tyr Asp Lys Leu Ile Val Arg
Phe 100 105 110Gly Ser Ser Lys Ile Asp Lys Glu Leu Val Asn Arg Ile
Glu Arg Ala 115 120 125Ile Gly Gln Lys Pro His Arg Phe Leu Arg Arg
Gly Ile Phe Phe Ser 130 135 140His Arg Asp Met Asn Gln Ile Leu Asp
Ala Tyr Glu Asn Lys Lys Pro145 150 155 160Phe Tyr Leu Tyr Thr Gly
Arg Gly Pro Ser Ser Glu Ala Met His Val 165 170 175Gly His Leu Ile
Pro Phe Ile Phe Thr Lys Trp Leu Gln Asp Val Phe 180 185 190Asn Val
Pro Leu Val Ile Gln Met Thr Asp Asp Glu Lys Tyr Leu Trp 195 200
205Lys Asp Leu Thr Leu Asp Gln Ala Tyr Gly Tyr Ala Val Glu Asn Ala
210 215 220Lys Asp Ile Ile Ala Cys Gly Phe Asp Ile Asn Lys Thr Phe
Ile Phe225 230 235 240Ser Asp Leu Asp Tyr Met Gly Ala Ser Pro Gly
Phe Tyr Lys Asn Val 245 250 255Val Lys Ile Gln Lys His Val Thr Phe
Asn Gln Val Lys Gly Ile Phe 260 265 270Gly Phe Thr Asp Ser Asp Ser
Ile Gly Lys Ile Ser Phe Pro Ala Ile 275 280 285Gln Ala Ala Pro Ser
Phe Ser Asn Ser Phe Pro Gln Ile Phe Gly Asp 290 295 300Lys Thr Asp
Val Gln Cys Leu Ile Pro Cys Ala Ile Asp Gln Asp Pro305 310 315
320Tyr Phe Arg Met Thr Arg Asp Val Ala Pro Arg Ile Gly Tyr Pro Lys
325 330 335Pro Ala Leu Leu His Ser Thr Phe Phe Pro Ala Leu Gln Gly
Ala Gln 340 345 350Thr Lys Met Ser Ala Ser Asp Pro Asn Ser Ser Ile
Phe Leu Thr Asp 355 360 365Thr Ala Lys Gln Ile Lys Thr Lys Val Asn
Lys His Ala Phe Ser Gly 370 375 380Gly Arg Asp Thr Val Glu Glu His
Arg Glu Phe Gly Gly Asn Cys Asp385 390 395 400Val Asp Val Ser Phe
Met Tyr Leu Thr Phe Phe Leu Glu Asp Asp Asp 405 410 415Arg Leu Glu
Gln Ile Arg Lys Asp Tyr Thr Ser Gly Ala Met Leu Thr 420 425 430Gly
Glu Leu Lys Lys Ile Leu Ile Glu Val Leu Gln Pro Leu Ile Ala 435 440
445Glu His Gln Ala Arg Arg Lys Glu Val Thr Asp Glu Ile Val Lys Glu
450 455 460Phe Met Thr Pro Arg Lys Leu Ser Tyr Asp Phe Gln465 470
475920DNAArtificial SequenceDescription of Artificial Sequence
Synthetic hTNF-alpha Forward primer 9ggagaagggt gaccgactca
201017DNAArtificial SequenceDescription of Artificial Sequence
Synthetic hTNF-alpha Reverse primer 10ctgcccagac tcggcaa
171126DNAArtificial SequenceDescription of Artificial Sequence
Synthetic hTrpRS Forward primer 11aagaattcat gcccaacagt gagccc
261232DNAArtificial SequenceDescription of Artificial Sequence
Synthetic hTrpRS Reverse primer 12aactcgagct accctggagg acagtcagcc
tt 321321DNAArtificial SequenceDescription of Artificial Sequence
Synthetic GAPDH forward primer 13cgctctctgc tcctcctgtt c
211422DNAArtificial SequenceDescription of Artificial Sequence
Synthetic GAPDH reverse primer 14ttgactccga ccttcacctt cc
221520DNAArtificial SequenceDescription of Artificial Sequence
Synthetic hMIP-1 alpha Forward primer 15accatggctc tctgcaacca
201620DNAArtificial SequenceDescription of Artificial Sequence
Synthetic hMIP-1 alpha Reverse primer 16ttaagaagag tcccacagtg
201721DNAArtificial SequenceDescription of Artificial Sequence
Synthetic hMIP-1 beta Forward primer 17agcctcacct ctgagaaaac c
211822DNAArtificial SequenceDescription of Artificial Sequence
Synthetic hMIP-1 beta Reverse primer 18gcaacagcag agaaacagtg ac
22
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