US2008220018A1PendingUtilityA1
Vaccine composition for vaccinating dogs against canine infectious respiratory disease(cird)
Est. expiryJul 1, 2023(expired)· nominal 20-yr term from priority
A61P 31/12A61P 37/04A61P 31/04A61P 11/00A61K 39/118A61K 39/0241G01N 2800/12A61K 2039/552G01N 33/6854A61K 2039/505G01N 2333/295G01N 2333/30A61K 39/092G01N 2333/315A61K 39/09
51
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Claims
Abstract
A vaccine composition for vaccinating dogs comprising any one or more of (a) an agent capable of raising an immune response against Streptococcus equi sub species zooepidemicus in a dog, (b) an agent capable of raising an immune response against Mycoplasma cynos in a dog, and (c) an agent capable of raising an immune response against a Chlamydophila in a dog.
Claims
exact text as granted — not AI-modified1 . A method of vaccinating a dog against canine infectious respiratory disease (CIRD), the method comprising administering to the dog a vaccine composition comprising an agent capable of raising an immune response against Streptococcus equi sub species zooepidemicus ( S. zooepidemicus ) in a dog.
2 . A method of treating CIRD in a dog, the method comprising administering to the dog a vaccine composition comprising an agent capable of raising an immune response against S. zooepidemicus in a dog.
3 . A method of stimulating an immune response against S. zooepidemicus in a dog, the method comprising administering to the dog an agent capable of raising an immune response against S. zooepidemicus in a dog.
4 . A method according to any of claims 1 to 3 wherein the agent capable of raising an immune response against Streptococcus equi sub species zooepidemicus ( S. zooepidemicus ) in a dog comprises an agent selected from the group consisting of inactivated or attenuated S. zooepidemicus , an immunogenic fragment of S. zooepidemicus or a derivative thereof, and a nucleic acid molecule encoding said fragment or said derivative.
5 . The method according to claim 1 or 2 further comprising administering to the dog an agent capable of raising an immune response against Mycoplasma cynos ( M. cynos ) in a dog.
6 . The method according to claim 5 wherein the agent capable of raising an immune response against M. cynos in a dog comprises an agent selected from the group consisting of inactivated or attenuated M. cynos, an immunogenic fragment of M. cynos or a derivative thereof, and a nucleic acid molecule encoding said fraction or said derivative.
7 . The method according to claim 1 or 2 further comprising administering to the dog an agent capable of raising an immune response against a Chlamydophila in a dog.
8 . The method according to claim 7 wherein the agent capable of raising an immune response in a dog against a Chlamydophila comprises an agent selected from the group consisting of inactivated or attenuated Chlamydophila abortus, Chlamydophila psittaci, Chlamydophila felis, Chlamydia muridarum, Chlamydia pecorum, Chlamydia pneumoniae, Chlamydia suis and Chlamydia trachomatis , an immunogenic fragment thereof or a derivative thereof, and a nucleic acid molecule encoding said fraction or said derivative.
9 . The method according to claim 1 or 2 further comprising administering to the dog any one or more of:
an agent capable of raising an immune response in a dog against canine respiratory coronavirus (CRCV); an agent capable of raising an immune response in a dog against canine parainfluenzavirus (CPIV); an agent capable of raising an immune response in a dog against canine adenovirus type 2 (CAV-2); an agent capable of raising an immune response in a dog against canine herpesvirus (CHV); and an agent capable of raising an immune response in a dog against Bordetella bronchiseptica ( B. bronchiseptica ).
10 . The method according to claim 9 wherein the agent capable of raising an immune response in a dog against CRCV comprises an agent selected from the group consisting of inactivated or attenuated CRCV, an immunogenic fragment thereof, and a nucleic acid molecule encoding said immunogenic fraction.
11 . The method according to claim 10 wherein the immunogenic fragment of CRCV comprises the Spike protein or the hemagglutinin-esterase (HE) protein, or an immunogenic portion of the Spike or HE protein.
12 . The method according to claim 9 wherein the agent capable of raising an immune response in a dog against CPIV comprises an agent selected from the group consisting of inactivated or attenuated CPIV, an immunogenic fragment thereof, and a nucleic acid molecule encoding said immunogenic fraction.
13 . The method according to claim 9 wherein the agent capable of raising an immune response in a dog against CAV-2 comprises an agent selected from the group consisting of inactivated or attenuated CAV-2, an immunogenic fragment thereof, and a nucleic acid encoding said immunogenic fraction.
14 . The method according to claim 9 wherein the agent capable of raising an immune response in a dog against CHV comprises an agent selected from the group consisting of inactivated or attenuated CHV, an immunogenic fragment thereof, and a nucleic acid molecule encoding said immunogenic fraction.
15 . The method according to claim 9 wherein the agent capable of raising an immune response in a dog against B. bronchiseptica comprises an agent selected from the group consisting of inactivated or attenuated B. bronchiseptica , an immunogenic fragment thereof, and a nucleic acid molecule encoding said immunogenic fraction.
16 . A method of determining whether a dog has or is susceptible to CIRD, the method comprising:
(a) obtaining a suitable sample from the dog; and (b) identifying S. zooepidemicus , or an antibody to S. zooepidemicus , in the sample.
17 . The method according to claim 16 wherein the S. zooepidemicus is identified using an antibody.
18 . The method according to claim 16 wherein the S. zooepidemicus is identified using a nucleic acid molecule.
19 . The method according to claim 16 wherein the anti-S. zooepidemicus antibody is identified using S. zooepidemicus or an antigenic portion thereof.
20 . The method according to claim 16 wherein the sample is an antibody-containing sample such as serum, saliva, tracheal wash or branchiolar lavage.Cited by (0)
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