Oral Respiratory Vaccines

Abstract

The present invention relates to new oral live canine parainfluenza virus vaccines and related multivalent vaccines. Methods of using the vaccines alone or in combination with one or more protective immunogens in a multivalent vaccine are also provided.

Description

[Technical Field]

[0001] CROSS-REFERENCE TO RELATED APPLICATIONS This application claims priority under 35 U.S.C. § 119(e) to provisional application U.S. 62 / 949,928, filed December 18, 2019, the contents of which are incorporated herein by reference in their entirety.

[0002] The present invention relates to new oral live canine parainfluenza virus vaccines and related multivalent vaccines. Methods for producing the vaccines and methods for using the vaccines, either alone or in combination with one or more other protective antigens in multivalent vaccines, are also provided. [Background technology]

[0003] Canine parainfluenza (CPI) virus is a highly contagious virus that causes respiratory disease contributing to upper respiratory tract disease and infectious bronchitis (also known as kennel cough). While respiratory signs may resemble those of canine influenza, they are unrelated viruses and require different vaccines for protection. CPI virus is shed from the respiratory tract of infected animals for up to two weeks after infection and is typically transmitted through the air. CPI virus spreads rapidly in barns and shelters where many dogs are housed together. Clinical signs include a dry or productive cough, mild fever, runny nose, lethargy, and loss of appetite.

[0004] Currently, there are several commercially available canine vaccines containing modified live CPI viruses that can be administered subcutaneously or intramuscularly, including Nobivac® Canine 1-DAPPv, a modified live virus vaccine for vaccinating healthy dogs to prevent diseases caused by canine parainfluenza virus, canine distemper virus, canine adenovirus, and canine parvovirus. Additionally, there are commercially available intranasal vaccines, such as Nobivac® Intra-Trac3, which provides triple protection against pathogens implicated in the cause of tracheobronchitis, including canine parainfluenza virus, canine adenovirus type 2, and Bordetella bronchiseptica (B. bronchiseptica). Summary of the Invention [Problem to be solved by the invention]

[0005] However, despite the advantages of oral vaccination, such as ease of use and minimal discomfort to the animal during and after vaccination, to date there have been no commercially available oral vaccines containing CPI viruses. Thus, there is a long-felt need for an oral vaccine for canine parainfluenza virus that will help protect dogs from upper respiratory tract disease and / or infectious tracheobronchitis.

[0006] The citation of any reference herein should not be construed as an admission that such reference is available as "Prior Art" to the instant application. [Means for solving the problem]

[0007] The present invention provides a vaccine composition for oral administration to an animal subject, such as a dog, comprising an immunologically effective amount of a modified live canine parainfluenza (CPI) virus useful for inducing (and / or providing effective protection against) protective immunity in the vaccinated animal subject. In certain embodiments, the titer of the modified live CPI virus in the vaccine is greater than or equal to 6.0 log 10 HAID 50 In another embodiment, the titer of the modified live CPI virus in the vaccine is 6.3 log / mL or greater. 10 HAID 50 In yet another embodiment, the titer of the modified live CPI virus in the vaccine is 6.5 log / mL or greater. 10 HAID 50 In yet another embodiment, the titer of the modified live CPI virus in the vaccine is 6.7 log / mL or greater. 10 HAID 50 In yet another embodiment, the titer of the modified live CPI virus in the vaccine is 6.9 log / mL or greater. 10 HAID 50 In yet another embodiment, the titer of the modified live CPI virus in the vaccine is 7.1 log / mL or greater. 10 HAID 50 In yet another embodiment, the titer of the modified live CPI virus in the vaccine is 7.3 log / mL or greater. 10 HAID 50 In yet another embodiment, the titer of the modified live CPI virus in the vaccine is 7.6 log / mL or greater. 10 HAID 50 In yet another embodiment, the titer of the modified live CPI virus in the vaccine is 7.8 log 10 HAID 50 In yet another embodiment, the titer of the modified live CPI virus in the vaccine is 8.0 log / mL or greater. 10 HAID 50 In yet another embodiment, the titer of the modified live CPI virus in the vaccine is 8.3 log / mL or greater. 10 HAID50 In yet another embodiment, the titer of the modified live CPI virus in the vaccine is 8.6 log / mL or greater. 10 HAID 50 In yet another embodiment, the titer of the modified live CPI virus in the vaccine is 8.8 log / mL or greater. 10 HAID 50 / mL or more.

[0008] In related embodiments of the oral vaccine, the titer of the modified live CPI virus in the vaccine is 6.0 log 10 HAID 50 / mL~9.5 log 10 HAID 50 In another embodiment of the oral vaccine, the titer of the modified live CPI virus in the vaccine is 6.5 log 10 HAID 50 / mL~9.5 log 10 HAID 50 In yet another embodiment, the titer of the modified live CPI virus in the vaccine is 6.8 log 10 HAID 50 / mL~9.5 log 10 HAID 50 In yet other embodiments, the titer of the modified live CPI virus in the vaccine is 7.0 log 10 HAID 50 / mL~9.5 log 10 HAID 50 In yet another embodiment, the titer of the modified live CPI virus in the vaccine is 7.3 log 10 HAID 50 / mL~9.5 log 10 HAID 50 In yet another embodiment, the titer of the modified live CPI virus in the vaccine is 7.3 log 10 HAID 50 / mL~8.6 log 10 HAID 50 / mL.

[0009] In certain embodiments of a vaccine comprising a modified live CPI virus, the CPI virus shares unique / identifying characteristics of the modified live CPI virus having ATCC accession number PTA-126273. In more specific embodiments, the modified live CPI virus in the vaccine has ATCC accession number PTA-126273.

[0010] The present invention further provides a vaccine for oral administration to an animal subject, which comprises a modified live canine parainfluenza (CPI) virus and further comprises avirulent live B. bronchiseptica, which aids in eliciting (and / or induces) protective immunity (and / or provides effective protection) in the vaccinated animal subject. In certain embodiments, in addition to comprising one of the above amounts of modified live CPI viruses, the vaccine further comprises 1 x 10 7 cfu / mL ~ 1 × 10 12 In another embodiment, the vaccine comprises a titer of live avirulent B. bronchiseptica equivalent to 1 x 10 cfu / mL. 8 cfu / mL ~ 1 × 10 12 In yet another embodiment, the vaccine comprises a titer of live avirulent B. bronchiseptica equivalent to 5 x 10 cfu / mL. 8 cfu / mL ~ 1 × 10 12 In yet another embodiment, the vaccine comprises a titer of live avirulent B. bronchiseptica equivalent to 1 x 10 cfu / mL. 9 cfu / mL ~5×10 11 Contains avirulent live B. bronchiseptica at a titer of cfu / mL.

[0011] The oral vaccines of the present invention may comprise a modified live canine parainfluenza virus with or without avirulent live B. bronchiseptica, along with one or more additional immunogens. In certain embodiments, the vaccine further comprises a live attenuated canine influenza virus. In other embodiments, the vaccine further comprises a live attenuated canine parvovirus. In yet other embodiments, the vaccine further comprises a live attenuated canine distemper virus. In yet other embodiments, the vaccine further comprises a live attenuated canine adenovirus type 2. In yet other embodiments, the vaccine further comprises a live attenuated canine respiratory coronavirus. In yet other embodiments, the vaccine further comprises a live attenuated canine pneumonia virus. In yet another embodiment, the vaccine further comprises a viral vector encoding one or more protein immunogens from canine influenza virus, canine parvovirus, canine distemper virus, canine adenovirus (type 1 or type 2), respiratory canine coronavirus, canine pneumonia virus, Streptococcus equi subsp. zooepidemicus, and / or Mycoplasma cynos. In yet another embodiment, the vaccine further comprises live attenuated Streptococcus equi subsp. zooepidemicus. In yet another embodiment, the vaccine further comprises live attenuated Mycoplasma cynos. Furthermore, vaccines comprising modified live canine parainfluenza virus or modified live canine parainfluenza virus along with avirulent live B. bronchiseptica further comprise two or more of these other immunogens. The vaccines of the present invention may be adjuvanted or unadjuvanted.

[0012] The present invention further provides a method for helping protect (and / or providing effective protection to) dogs against upper respiratory tract disease and infectious tracheobronchitis, comprising orally administering to the dog a vaccine comprising a modified live canine parainfluenza virus. In certain embodiments of this method, the titer of the administered modified live canine parainfluenza virus is greater than or equal to 6.0 log 10 HAID 50 In another embodiment of this method, the titer of the administered modified live CPI virus is 6.3 log 10 HAID 50 In yet another embodiment of this method, the titer of the administered modified live CPI virus is 6.5 log 10 HAID 50 In yet another embodiment of this method, the titer of the administered modified live CPI virus is 6.7 log 10 HAID 50 In yet another embodiment of this method, the potency of the modified live CPI administered is 7.0 log / dose or greater. 10 HAID 50 In yet another embodiment of this method, the titer of the administered modified live CPI virus is 7.3 log 10 HAID 50 In yet another embodiment of this method, the titer of the modified live CPI administered is 7.6 log / dose or greater. 10 HAID 50 In yet another embodiment of this method, the titer of the administered modified live CPI virus is 7.8 log 10 HAID 50 In yet another embodiment of this method, the titer of the modified live CPI administered is 8.0 log / dose or greater. 10 HAID 50 In yet another embodiment of this method, the titer of the administered modified live CPI virus is 8.3 log 10 HAID 50In yet another embodiment of this method, the titer of the modified live CPI administered is 8.6 log / dose or greater. 10 HAID 50 In yet another embodiment of this method, the titer of the administered modified live CPI virus is 8.8 log 10 HAID 50 / dose or more.

[0013] In a related embodiment of this method, the titer of the administered modified live CPI virus is 6.0 log 10 HAID 50 / dose~9.5 log 10 HAID 50 In another embodiment of this method, the titer of the administered modified live CPI virus is 6.3 log 10 HAID 50 / dose~9.5 log 10 HAID 50 In yet another embodiment of this method, the titer of the administered modified live CPI virus is 6.5 log 10 HAID 50 / dose~9.5 log 10 HAID 50 In yet another embodiment of this method, the titer of the administered modified live CPI virus is 6.8 log 10 HAID 50 / dose~9.5 log 10 HAID 50 In yet another embodiment of this method, the titer of the administered modified live CPI virus is 7.0 log 10 HAID 50 / dose~9.5 log 10 HAID 50 In yet another embodiment of this method, the titer of the administered modified live CPI virus is 7.3 log 10 HAID 50 / dose~9.5 log 10 HAID 50In yet another embodiment of this method, the titer of the administered modified live CPI virus is 7.3 log 10 HAID 50 / dose~9.0 log 10 HAID 50 In certain embodiments of the method of orally administering a vaccine comprising a modified live CPI virus, the CPI virus shares unique / identifying characteristics of the modified live CPI virus having ATCC accession number PTA-126273. In more specific embodiments of the method of the present invention, the modified live CPI virus has ATCC accession number PTA-126273.

[0014] In one aspect of the present invention, the method for helping to protect dogs (and / or provide effective protection to dogs) from upper respiratory tract disease and infectious tracheobronchitis comprises orally administering to an animal subject, such as a dog, a vaccine comprising a modified live CPI virus that further comprises live avirulent B. bronchiseptica (i.e., a vaccine comprising both a modified live CPI virus and live avirulent B. bronchiseptica).

[0015] In certain embodiments of this method, in addition to containing one of the amounts of modified live CPI viruses, the vaccine comprises 1 x 10 7 cfu / dose. In certain embodiments of this method, the titer of the avirulent live B. bronchiseptica is 5×10 7 In a more particular embodiment of this method, the titer of said avirulent live B. bronchiseptica is 1 x 10 cfu / dose or greater. 8 In an even more particular embodiment of this method, the titer of said avirulent live B. bronchiseptica is 5 x 10 cfu / dose or greater. 8In certain embodiments, the titer of the avirulent live B. bronchiseptica is 1 x 10 cfu / dose or greater. 9 In a related embodiment of this method, the titer of the avirulent live B. bronchiseptica is 1 x 10 cfu / dose or greater. 7 cfu / dose~1×10 12 In yet another embodiment of this method, the titer of the avirulent live B. bronchiseptica is 1 x 10 cfu / dose. 9 cfu / dose~1×10 12 In yet another embodiment of this method, the titer of the avirulent live B. bronchiseptica is 1 x 10 cfu / dose. 8 cfu / dose~5×10 11 In yet another embodiment of this method, the titer of the avirulent live B. bronchiseptica is 5 x 10 cfu / dose. 8 cfu / dose~5×10 11 In yet another embodiment of this method, the titer of the avirulent live B. bronchiseptica is 1 x 10 cfu / dose. 9 cfu / dose~5×10 11 In yet another embodiment of this method, the titer of the avirulent live B. bronchiseptica is 5 x 10 cfu / dose. 9 cfu / dose~5×10 11 cfu / dose.

[0016] In a more particular embodiment of the method, the titer of the modified live CPI virus is 6.0 log 10 HAID 50 / dose or more, and the titer of the avirulent live B. bronchiseptica is 1 x 10 7 In an even more particular embodiment of the method, the titer of the modified live CPI virus is 6.5 log 10 HAID50 / dose or more, and the titer of the avirulent live B. bronchiseptica is 1 x 10 7 In an even more particular embodiment of the method, the titer of the modified live CPI virus is 6.5 log 10 HAID 50 / dose or more, and the titer of the avirulent live B. bronchiseptica is 5 x 10 8 cfu / dose or more.

[0017] In certain embodiments of the method, the titer of the modified live CPI virus is 6.0 log 10 HAID 50 / dose or more ~9.5 log 10 HAID 50 / dose, and the titer of the avirulent live B. bronchiseptica is 1 x 10 7 In another embodiment of the method, the titer of the modified live CPI virus is 6.5 log cfu / dose or greater. 10 HAID 50 / dose or more ~9.5 log 10 HAID 50 / dose, and the titer of the avirulent live B. bronchiseptica is 1 x 10 7 In yet another embodiment of this method, the titer of the modified live CPI virus is 6.8 log cfu / dose or greater. 10 HAID 50 / dose~9.5 log 10 HAID 50 / dose, and the titer of the avirulent live B. bronchiseptica is 1 x 10 7 In yet another embodiment of this method, the titer of the modified live CPI virus is 6.8 log cfu / dose or greater. 10 HAID 50 / dose~9.5 log 10 HAID 50 / dose, and the titer of the avirulent live B. bronchiseptica is 1 x 10 9 In yet other embodiments, the titer of the modified live CPI virus is 7.0 log 10 HAID 50 / dose~9.0 log 10 HAID 50 / dose, and the titer of the avirulent live B. bronchiseptica is 1 x 10 7 In yet other embodiments, the titer of the modified live CPI virus is 7.0 log 10 HAID 50 / dose~9.0 log 10 HAID 50 / dose, and the titer of the avirulent live B. bronchiseptica is 1 x 10 9 cfu / dose or more.

[0018] In yet another embodiment of this method, the titer of the modified live CPI virus is 6.0 log 10 HAID 50 / dose or more, and the titer of the avirulent live B. bronchiseptica is 5 x 10 8 cfu / dose~5×10 11 cfu / dose. In yet another embodiment of this method, the titer of the modified live CPI virus is 6.5 log 10 HAID 50 / dose or more, and the titer of the avirulent live B. bronchiseptica is 5 x 10 8 cfu / dose~5×10 11 cfu / dose. In yet another embodiment of this method, the titer of the modified live CPI virus is 6.5 log 10 HAID 50 / dose or more, and the titer of the avirulent live B. bronchiseptica is 5 x 10 9 cfu / dose~5×10 11 cfu / dose.

[0019] In another embodiment of this method, the titer of the modified live CPI virus is 6.0 log 10 HAID 50 / dose~9.5 log 10 HAID 50 / dose, and the titer of the avirulent live B. bronchiseptica is 5 x 10 8 cfu / dose~5×10 11 cfu / dose. In yet another embodiment of this method, the titer of the modified live CPI virus is 6.5 log 10 HAID 50 / dose~9.5 log 10 HAID 50 / dose, and the titer of the avirulent live B. bronchiseptica is 5 x 10 8 cfu / dose~5×10 11 cfu / dose. In yet other embodiments, the titer of the modified live CPI virus is 6.5 log 10 HAID 50 / dose~9.5 log 10 HAID 50 / dose, and the titer of the avirulent live B. bronchiseptica is 5 x 10 9 cfu / dose~5×10 11 cfu / dose. In yet another embodiment of this method, the titer of the modified live CPI virus is 6.8 log 10 HAID 50 / dose~9.0 log 10 HAID 50 / dose, and the titer of the avirulent live B. bronchiseptica is 5 x 10 8 cfu / dose~5×10 11 cfu / dose. In yet another embodiment of this method, the titer of the modified live CPI virus is 6.8 log 10 HAID 50 / dose~9.5 log 10 HAID 50 / dose, and the titer of the avirulent live B. bronchiseptica is 5 x 10 9 cfu / dose~5×10 11 cfu / dose. In yet other embodiments, the titer of the modified live CPI virus is 7.0 log 10 HAID 50 / dose~9.0 log 10 HAID 50 / dose, and the titer of the avirulent live B. bronchiseptica is 5 x 10 8 cfu / dose~5×10 11 cfu / dose. In yet other embodiments, the titer of the modified live CPI virus is 7.0 log 10 HAID 50 / dose~9.0 log 10 HAID 50 / dose, and the titer of the avirulent live B. bronchiseptica is 5 x 10 9 cfu / dose~5×10 11 cfu / dose.

[0020] In a particular embodiment of the method for orally administering a vaccine comprising a modified live CPI virus and avirulent live B. bronchiseptica, the avirulent live B. bronchiseptica virus shares unique / identifying characteristics with the avirulent live B. bronchiseptica having ATCC accession number PTA-126272. In a more particular embodiment of the method, the avirulent live B. bronchiseptica has ATCC accession number PTA-126272. In an even more particular embodiment, the modified live CPI virus has ATCC accession number PTA-126273 and the avirulent live B. bronchiseptica has ATCC accession number PTA-126272.

[0021] In another embodiment, a method for assisting in the protection of dogs (and / or providing effective protection to dogs) from upper respiratory tract disease and infectious tracheobronchitis comprises orally administering a vaccine comprising a modified live canine parainfluenza virus and one or more additional immunogens. In certain embodiments of the method, the vaccine further comprises a live attenuated canine influenza virus. In other species of embodiments of the method, the vaccine further comprises a live attenuated canine parvovirus. In yet other species of embodiments of the method, the vaccine further comprises a live attenuated canine distemper virus. In yet other species of embodiments of the method, the vaccine further comprises a live attenuated canine adenovirus type 2. In yet other species of embodiments of the method, the vaccine further comprises a live attenuated canine respiratory coronavirus. In yet other species of embodiments of the method, the vaccine further comprises a live attenuated canine pneumonia virus. In yet another species of the method, the vaccine further comprises one or more viral vectors encoding one or more protein immunogens from canine influenza virus, canine parvovirus, canine distemper virus, canine adenovirus (type 1 or type 2), respiratory canine coronavirus, canine pneumonia virus, Streptococcus equi subsp. zooepidemicus, and / or Mycoplasma cynos. In yet another species of the method, the vaccine further comprises live attenuated Streptococcus equi subsp. zooepidemicus. In yet another species of the method, the vaccine further comprises live attenuated Mycoplasma cynos. Additionally, methods of assisting in the protection of dogs from upper respiratory tract disease and infectious tracheobronchitis (and / or methods of providing effective protection to dogs) can include orally administering a vaccine comprising a modified live canine parainfluenza virus in combination with two or more of these immunogens.

[0022] In related embodiments, a method for assisting in the protection of dogs (and / or providing effective protection to dogs) from upper respiratory tract disease and infectious tracheobronchitis comprises orally administering to the dog a vaccine comprising a modified live canine parainfluenza virus, avirulent live B. bronchiseptica, and one or more additional live attenuated immunogens. In certain embodiments of the method, the vaccine further comprises a live attenuated canine influenza virus. In other species of the method, the vaccine further comprises a live attenuated canine parvovirus. In yet other species of the method, the vaccine further comprises a live attenuated canine distemper virus. In yet other species of the method, the vaccine further comprises a live attenuated canine adenovirus type 2. In yet other species of the method, the vaccine further comprises a live attenuated canine respiratory coronavirus. In yet other species of the method, the vaccine further comprises a live attenuated canine pneumonia virus. In yet another species of the method, the oral vaccine further comprises a viral vector encoding one or more protein immunogens from canine influenza virus, canine parvovirus, canine distemper virus, canine adenovirus (type 1 or type 2), respiratory canine coronavirus, canine pneumonia virus, Streptococcus equi subsp. zooepidemicus, and / or Mycoplasma cynos. In yet another species of the method, the vaccine further comprises live attenuated Streptococcus equi subsp. zooepidemicus. In yet another species of the method, the vaccine further comprises live attenuated Mycoplasma cynos.Additionally, methods of assisting in the protection of dogs from the above-mentioned upper respiratory tract diseases and infectious tracheobronchitis (and / or methods of providing effective protection to dogs) can include orally administering a vaccine comprising a modified live canine parainfluenza virus and avirulent B. bronchiseptica in combination with two or more of these immunogens.

[0023] In certain embodiments, a method for assisting in the protection of dogs (and / or providing effective protection to dogs) from upper respiratory tract disease and infectious tracheobronchitis comprises orally administering a vaccine comprising a modified live canine parainfluenza virus, a live attenuated canine parvovirus, a live attenuated canine distemper virus, a live attenuated canine adenovirus type 2, and avirulent live B. bronchiseptica.

[0024] In certain embodiments, the methods of the present invention for assisting in the protection of dogs from upper respiratory tract disease and infectious tracheobronchitis (and / or providing effective protection to dogs) can comprise orally administering a single dose of a vaccine to the dog. Thus, in particular embodiments, the methods comprise orally administering to the dog a single dose of a vaccine comprising a modified live canine parainfluenza virus. In related embodiments, the methods comprise orally administering to the dog a single dose of a vaccine comprising both a modified live canine parainfluenza virus and avirulent live B. bronchiseptica.

[0025] In another embodiment, a method of assisting in the protection of dogs from upper respiratory tract disease and infectious tracheobronchitis (and / or providing effective protection to dogs) of the present invention can comprise orally administering to the dog two or more doses of a vaccine. Thus, in certain embodiments, the method comprises orally administering to the dog two or more doses of a vaccine comprising a modified live canine parainfluenza virus. In a related embodiment, the method comprises orally administering to the dog two or more doses of a vaccine comprising both a modified live canine parainfluenza virus and avirulent live B. bronchiseptica.

[0026] In certain embodiments, methods of assisting in the protection of dogs from upper respiratory tract disease and infectious tracheobronchitis (and / or methods of providing effective protection to dogs) comprise orally administering to the dog an unadjuvanted vaccine. Particular embodiments of these methods comprise orally administering to the dog a vaccine comprising a modified live canine parainfluenza virus, wherein the vaccine is an unadjuvanted vaccine. More particular embodiments of these methods comprise orally administering to the dog a vaccine comprising a modified live canine parainfluenza virus and avirulent live B. bronchiseptica, wherein the vaccine is an unadjuvanted vaccine. In certain embodiments of this type, the vaccine is administered as a single dose vaccine.

[0027] Another embodiment of a method for assisting in the protection of dogs from upper respiratory tract disease and infectious tracheobronchitis (and / or providing effective protection to dogs) comprises orally administering to the dog an adjuvanted vaccine. Particular embodiments of these methods comprise orally administering to the dog a vaccine comprising a modified live canine parainfluenza virus, the vaccine comprising an adjuvant. A related embodiment of these methods comprises orally administering to the dog a vaccine comprising both a modified live canine parainfluenza virus and avirulent live B. bronchiseptica, the vaccine comprising an adjuvant. In particular embodiments of this type, the vaccine is administered as a single-dose vaccine.

[0028] In certain embodiments of the methods of assisting in the protection of dogs from upper respiratory tract disease and infectious tracheobronchitis (and / or providing effective protection to dogs), the vaccines of the invention are orally administered in a dose of 0.2 mL to 5 mL. In related embodiments, the vaccines of the invention are orally administered in a dose of 0.2 mL to 4 mL. In certain other embodiments, the vaccines of the invention are orally administered in a dose of 0.3 to 1.5 mL. In still other embodiments, the vaccines of the invention are orally administered in a dose of 0.2 mL to 3.0 mL. In still other embodiments, the vaccines of the invention are orally administered in a dose of 0.2 mL to 2.5 mL. In still other embodiments, the vaccines of the invention are orally administered in a dose of 0.2 mL to 2.0 mL. In still other embodiments, the vaccines of the invention are orally administered in a dose of 0.5 to 2.5 mL. In still other embodiments, the vaccines of the invention are orally administered in a dose of 0.75 mL to 2.0 mL. In still other embodiments, the vaccines of the invention are orally administered in a dose of 0.5 mL to 2.0 mL. In yet another embodiment, the vaccine of the present invention is orally administered in a dose of 0.5 mL to 1.5 mL. In yet another embodiment, the vaccine of the present invention is orally administered in a dose of 0.75 mL to 1.5 mL. In a specific embodiment, the vaccine of the present invention is orally administered in a dose of 1.0 mL.

[0029] These and other aspects of the present invention will be better understood by reference to the following detailed description, including the examples that follow. DETAILED DESCRIPTION OF THE INVENTION

[0030] Thus, the present invention provides modified live canine parainfluenza virus vaccines, including multivalent vaccines useful as oral vaccines. The present invention also provides methods for orally immunizing dogs against canine parainfluenza virus, comprising orally administering to the dog a vaccine comprising a modified live canine parainfluenza (CPI) virus. The present invention further provides single-dose vaccines comprising the modified live canine parainfluenza virus. Such vaccines support protection of vaccinated dogs (and / or provide effective protection to dogs) against upper respiratory tract disease and infectious tracheobronchitis for at least six months without the need for booster vaccines. In certain embodiments, the single-dose vaccine is administered to dogs in a 1 mL dose.

[0031] The present invention further provides vaccines comprising a modified live canine parainfluenza virus in combination with one or more other canine pathogens and / or immunogens that further elicit immunity against canine influenza virus (e.g., H3N2 and / or H3N8), canine parvovirus, canine distemper virus, canine adenovirus, canine respiratory coronavirus, canine pneumonia virus, Mycoplasma spp. (e.g., Mycoplasma cynos), and Streptococcus equi subsp. zooepidemicus.

[0032] More specifically, the present invention also includes a multivalent oral vaccine comprising a modified live canine parainfluenza virus in combination with live avirulent B. bronchiseptica. The present invention further provides a method of immunizing a dog against canine parainfluenza virus and B. bronchiseptica, comprising orally administering to the dog a vaccine comprising the modified live canine parainfluenza virus and live avirulent B. bronchiseptica. In certain embodiments of the present invention, dogs receiving only one dose of a single-dose vaccine (or multivalent vaccine) comprising a modified live canine parainfluenza virus and live avirulent B. bronchiseptica are protected against upper respiratory tract disease and infectious tracheobronchitis caused by wild-type CPI virus and live wild-type avirulent B. bronchiseptica for at least six months without the need for a booster vaccine. In a more particular embodiment, said single dose vaccine is administered to a dog in a 1 mL dose.

[0033] In certain embodiments, the vaccine comprises an immunologically effective amount of modified live CPI virus and avirulent live B. bronchiseptica, as determined by the amount of CPI virus serum neutralizing antibodies and B. bronchiseptica agglutination and / or IgA antibodies elicited in vaccinated dogs. In a related aspect, the invention provides a vaccine comprising a specific minimal amount of each antigen that is effective against virulent CPI virus and virulent B. bronchiseptica. In yet another aspect, the vaccine of the invention is safe and effective and helps protect (and / or provides effective protection to) dogs from upper respiratory tract disease and infectious tracheobronchitis due to CPI virus and B. bronchiseptica infection in dogs.

[0034] The present invention also provides a multivalent vaccine comprising a live attenuated CPI virus and avirulent live B. bronchiseptica in further combination with one or more other canine pathogens and / or immunogens that further elicit immunity against canine influenza virus (e.g., H3N2 and H3N8), canine parvovirus, canine adenovirus, canine distemper virus, canine adenovirus, canine respiratory coronavirus, canine pneumonia virus, Mycoplasma spp. (e.g., Mycoplasma cynos), and Streptococcus equi subsp. zooepidemicus.

[0035] As used herein, the term "approximately" is used interchangeably with the term "about" and means that a numerical value is within 25% of the specified value, i.e., a dose of vaccine containing "approximately" 4.0 mL can contain between 3.0 and 5.0 mL.

[0036] As used herein, the term "canine" is used interchangeably with the term "dog" and includes all domestic dogs, i.e., Canis lupus familiaris or Canis familiaris, unless otherwise specified.

[0037] As used herein, the term "cat" refers to any member of the Felidae family. Domestic cats, purebred and / or mixed breed pet cats, and wild or feral cats are all cats.

[0038] As used herein, a "vaccine" is a vaccine suitable for administration to animals, e.g., dogs, that contains one or more antigens, i.e., one or more immunogens, in combination with a pharmaceutically acceptable carrier, typically a liquid comprising sterile water, and that, upon administration to an animal, induces an immune response that is sufficiently strong to at least support protection (and / or provide effective protection) from disease resulting from infection with a wild-type microorganism (e.g., a virus or bacterium), i.e., sufficiently strong to support prevention of disease, provide effective protection, or prevent or ameliorate disease. In a preferred embodiment, the vaccine is sufficiently strong to provide effective protection from disease resulting from infection with a wild-type microorganism (e.g., a virus or bacterium). Herein, the use of the term "vaccine" encompasses both monovalent and polyvalent vaccines. Vaccines for oral administration to animal subjects may also be referred to as "oral vaccines."

[0039] As used herein, a "multivalent vaccine" is a vaccine that contains two or more different antigens. In certain embodiments of this type, the multivalent vaccine stimulates the recipient's immune system against two or more different pathogens.

[0040] As used herein, the terms "protect," "protecting," "provides effective protection," "providing effective protection," "aids in the protection," "aiding in the protection," and "aids in eliciting protective immunity" do not require complete protection from any manifestation of infection. For example, "aiding in the protection" can mean that protection is sufficient such that, after challenge, the underlying symptoms of infection are at least alleviated and / or one or more of the underlying cellular, physiological, or biochemical causes or mechanisms that cause the symptoms are alleviated and / or eliminated. "Alleviation," as used in this context, is understood to refer to the state of infection, including the molecular state of infection, rather than simply the physiological state of infection.

[0041] As used herein, the terms "providing effective protection" and "providing effective protection" are used interchangeably. With respect to the modified live canine parainfluenza virus comprised by the vaccines of the present invention, "providing effective protection" in dogs from upper respiratory tract disease and infectious tracheobronchitis is determined by finding a statistically significant reduction in the duration of CPI virus shedding and / or clinical signs of disease between vaccinated and placebo-vaccinated control dogs following challenge with live wild-type CPI virus. With respect to the live avirulent B. bronchiseptica comprised by the vaccines of the present invention, "providing effective protection" in dogs from upper respiratory tract disease and infectious tracheobronchitis is determined by finding a statistically significant reduction in the number of diseased dogs between vaccinated and placebo-vaccinated dogs following challenge with live wild-type B. bronchiseptica. Affected dogs are defined as having spontaneous cough or spontaneous cough with retching for 2 or more consecutive days during the post-challenge observation period.

[0042] As used herein, "duration of viral shedding" is the number of days from the first to last occurrence of virus shedding from a dog's nasal passages, as measured by viral titration from a nasal swab. In certain embodiments of the invention, the duration of viral shedding is measured for CPI viruses.

[0043] As used herein, "duration of bacterial shedding" is the number of days from the first to last occurrence of bacteria shedding from a dog's nasal passages, as measured by bacterial titration from a nasal swab. In certain embodiments of the invention, the duration of bacterial shedding is measured for B. bronchiseptica.

[0044] As used herein, a dog that "seroconverts" means that the dog's antibody titer to a particular antigen (e.g., CPI virus or B. bronchiseptica) is at least two-fold greater than the baseline value for that particular antigen.

[0045] As used herein, the terms "live attenuated virus" and "modified live virus" are used interchangeably and refer to an attenuated live virus immunogen that is immunogenic but not pathogenic.

[0046] As used herein, the terms "attenuated bacteria," "live avirulent culture of bacteria," and "live avirulent bacteria" are used interchangeably and refer to live attenuated bacterial immunogens (e.g., live avirulent B. bronchiseptica) that are immunogenic but not pathogenic.

[0047] As used herein, when a "dose" of vaccine administered to an animal subject is defined as containing a particular amount or range of amounts of antigen, e.g., by weight, such as 4 μg / dose or 2-6 μg / dose, or by titer, such as 7.3 loglOHAID50 / dose or 7.3-8.6 loglOHAID50 / dose, administration of the entire dose can be carried out in a single administration or can be carried out in multiple administrations spaced 3 hours or less apart. In certain embodiments, the vaccine doses are orally administered to the animal subject all at once in a single administration.

[0048] As used herein, a "single-dose vaccine" is a vaccine (or multivalent vaccine) that includes at least one immunogen from a pathogen, which vaccine (or multivalent vaccine) is administered to an animal in a single dose or in multiple doses over a short period of time, i.e., spaced apart by no more than three hours, and which aids in the protection of the animal (and / or provides effective protection to the animal) from the pathogen for at least six months, again without the need for a second dose of vaccine (e.g., a booster vaccine). In certain embodiments of this type, the single-dose vaccine is administered orally to an animal subject, e.g., a dog, as a single aliquot of vaccine, all in a single administration. In certain embodiments, the single-dose vaccine is administered orally to an animal subject in a 1 mL dose. Thus, it is contemplated that the vaccine of the present invention can be administered orally to an animal subject, e.g., a dog, as a single-dose vaccine with a duration of immunity of at least six months. In certain embodiments, the duration of immunity is at least nine months. In other embodiments, the duration of immunity is at least twelve months. In still other embodiments, the duration of immunity is at least eighteen months.

[0049] In another aspect, a second dose of the vaccine (or multivalent vaccine) is administered one week, multiple weeks, or several months after the first dose, over a period of 6 to 18 months after the initial oral administration. Booster vaccines can be administered by injection (e.g., intramuscularly, subcutaneously), intranasally, or orally. Thus, in some embodiments, at least two doses of the vaccine are administered orally. In some such embodiments, for example, the vaccine is administered twice, with the second dose (e.g., a booster vaccine) being administered at least about two weeks after the initial vaccine. In some embodiments, the vaccine is administered twice, with the second dose being administered up to eight weeks after the first dose. In other embodiments, the second dose is administered about two weeks to about four months after the first dose, about two weeks to about eight weeks after the first dose, or about three weeks to about four weeks after the first dose. In some embodiments, the second dose is administered about four weeks after the first dose. The first and subsequent doses may vary, for example, in amount and / or form. However, in many cases, the dosage will be the same in terms of amount and form. It should be understood that whether the administration is as a single dose vaccine or multiple doses (i.e., booster vaccine(s)), subsequent administrations of vaccine may need to be provided to a given animal subject after a 6-18 month duration of immunity (or even longer), such as an annual or biennial administration regimen.

[0050] Where a single dose of an oral vaccine of the invention is sufficient to support protection of an animal from a pathogen (and / or provide effective protection to an animal) for at least six months, the amount of antigen in that dose generally comprises a therapeutically effective amount of vaccine for a duration of six months or more. On the other hand, where a booster vaccine dose is required to supplement the primary dose, the combined amount of primary vaccine and booster vaccine may constitute a therapeutically effective amount.

[0051] The terms "adjuvant" and "immunostimulant" are used interchangeably herein and are defined as one or more substances that cause stimulation of the immune system.

[0052] As used herein, a "non-adjuvanted vaccine" is a vaccine or multivalent vaccine that does not contain an adjuvant.

[0053] As used herein, the term "pharmaceutically acceptable" is used adjectively to mean that the modified noun is appropriate for use in a pharmaceutical product. For example, when used to describe an excipient in a pharmaceutical vaccine, it characterizes the excipient as being compatible with the other components of the composition and not adversely harmful to the intended recipient animal, e.g., a dog.

[0054] In certain embodiments, the vaccines of the present invention can also be administered with a pharmaceutically acceptable immunostimulant and / or adjuvant and / or bioadhesive polymer. In this context, an adjuvant is used to enhance the immune response to one or more vaccine antigens / isolates. Thus, an "adjuvant" is an agent that nonspecifically increases the immune response to a particular antigen, thereby reducing the amount of antigen required in a given vaccine and / or the number of injections required to generate a sufficient immune response to the antigen of interest. Suitable adjuvants for animal vaccination include, but are not limited to, mineral gels such as aluminum hydroxide, aluminum phosphate, and alum; surfactants such as pluronic polyols; and oil emulsions. One adjuvant exemplified below, CARBIGEN™, is a terminally sterilized carbomer-based (CARBOPOL® 934P) adjuvant suspension containing emulsifying components, free of animal-derived components, available from MVP Adjuvants, 4805 "G" Street, Omaha, NE. CARBOPOL® 934P is an acrylic acid homopolymer crosslinked with allyl sucrose or allyl pentaerythritol.

[0055] The bioadhesive polymer PVP-K60 is a hygroscopic, amorphous, linear nonionic polyvinylpyrrolidone polymer that is soluble in water and organic solvents and is pH stable (K60 refers to its molecular weight).

[0056] Information regarding adjuvants and various aspects of immunoassays is disclosed, for example, in the series by P. Tijssen, "Practice and Theory of Enzyme Immunoassays," 3rd Edition, 1987, Elsevier, New York, which is incorporated herein by reference. Pharmaceutically acceptable immunostimulating agents include bacterial and / or fungal cell wall components (e.g., lipopolysaccharides, lipoproteins, glycoproteins, muramyl peptides), mucoadhesive polymers, various complex carbohydrates of plant origin (e.g., glycans, acemannan), various proteins and peptides of animal origin (e.g., hormones, cytokines, costimulatory factors), and novel nucleic acids (e.g., double-stranded RNA, CpG) derived from viruses and / or other sources.

[0057] Live attenuated CPI viruses for use in the vaccines of the present invention can be prepared by conventional means, including, for example, modifying virulent strains by in vitro passaging, cold adaptation, modifying the virulence of organisms by genetic engineering, selecting nonpathogenic wild-type strains, and other methods well known to those of skill in the art. Such attenuated CPI viruses can then be tested to determine whether they are suitable for oral administration, as detailed in the Examples below.

[0058] Modified live CPI virus strains can be derived by serial passage of wild-type virus through cell culture. In another embodiment, modified live CPI virus strains are derived by serial passage of wild-type virus through laboratory and / or non-host animals. The accumulation of genetic mutations during such passages typically results in a gradual loss of pathogenicity of the organism against the original host. In some embodiments, attenuated live virus strains are prepared by cold adaptation. Cold-adapted viruses have the advantage of replicating only at temperatures found in the upper respiratory tract. Methods for generating cold-adapted equine influenza viruses are described in U.S. Pat. No. 6,177,082, which is incorporated herein by reference in its entirety. The resulting desired cold-adapted virus confers one or more of the following phenotypes: cold adaptation, temperature sensitivity, dominant interference, and / or attenuation. Furthermore, both modified live canine parainfluenza viruses and avirulent live B. bronchiseptica have previously been disclosed and are included in commercially available canine vaccines.

[0059] biological deposit Cultures of the following biological material have been deposited under conditions satisfying the requirements of the Budapest Treaty with the following international depository: American Type Culture Collection (ATCC), 10801 University Boulevard, Manassas, Va. 20110-2209, USA. All restrictions imposed by the depositor on making the deposit available to the public will be irrevocably removed upon the granting of a patent. [Table 1]

[0060] The following examples serve to provide further understanding of the present invention, but are not meant to limit the effective scope of the invention in any way. [Example]

[0061] Example 1 Efficacy of oral canine parainfluenza virus and B. bronchiseptica vaccines administered with or without bioadhesive polymers or bioadhesive adjuvants Materials and Methods vaccine: The experimental vaccine contained avirulent live B. bronchiseptica antigen B-C2, ATCC accession number PTA-126272, and modified live CPI virus, strain Cornell, antigen ATCC accession number PTA-126273, mixed with a stabilizer solution [hydrolyzed gelatin, NZ amine AS (enzymatic hydrolyzate of casein obtained from Millipore Sigma, Burlington, MA), sorbitol-d, and dibasic sodium phosphate] and then lyophilized. The vaccine administered to dogs in treatment groups A, C, and D contained 10-15% CARBIGEN™ as an adjuvant. The vaccine administered to dogs in treatment group C also contained PVP-K60, a bioadhesive polymer.

[0062] The vaccine CPI virus titer was 7.5–8.5 log 10 HAID 50 / mL, while the B. bronchiseptica titer of the vaccine was 9.2 × 10 9 ~1.4×10 10 All vaccines were freeze-dried in vials, and on the day of vaccination, each vial of freeze-dried vaccine was rehydrated with 1 mL of sterile water, and similar preparations were pooled. CPI virus titers were measured using a log 10 HAID 50 The values ​​are given in units of / mL, which is a commonly used unit to estimate the concentration of virus in a sample calculated by the Spearman-Koerber method.

[0063] animal: Seven 10-week-old beagles (Marshall Bioresources) were housed together in a BSL-2 facility on a concrete floor covered with wood shavings, with food and water available ad libitum.

[0064] Vaccination and serum collection: On Study Day 0, dogs in Treatment Group D were inoculated orally with a 1 mL dose of vaccine consisting of CPI virus, B. bronchiseptica (Bb), and 15% CARBIGEN™. A spray device was attached to the syringe to deliver the vaccine to the back of the throat. On Study Day 14, all dogs were inoculated orally with the respective pooled vaccines (see Table 1 below). On Study Day 27, whole blood was collected by venipuncture of the jugular vein. Serum was separated by centrifugation and stored at or below -10°C until testing.

[0065] Detection of CPI virus neutralizing antibodies: A standard serum neutralization (SN) assay was used to detect CPI virus-neutralizing antibodies. Serum dilutions were incubated with the CPI virus vaccine strain and inoculated into canine kidney cells. After 5–7 days, monolayers were fixed and stained with fluorescein-conjugated CPI virus antiserum, and SN antibody titers were calculated as the reciprocal of the serum dilution that caused 50% inhibition of virus infection.

[0066] Table 1 Test Design [Table 2]

[0067] Challenge: On study day 28, dogs were challenged with virulent CPI virus.

[0068] Post-challenge observations and samples: Clinical observations were recorded for 11 days after challenge, and nasal swabs were collected daily for 11 days after challenge.

[0069] result Serology: Prior to vaccination, all dogs had CPI virus serum neutralizing titers of less than 2, indicating that the dogs were virus-free at the time of vaccination. Placebo-vaccinated control dogs remained seronegative (SN<2) until immediately prior to vaccination. Nearly all dogs in each treatment group seroconverted (titers >4) after vaccination [see Table 2 below].

[0070] Table 2 Serum antibody titers against CPI virus [Table 3]

[0071] CPI viral shedding: Duration of CPI virus shedding was the primary variable for assessing vaccine efficacy. For each animal, the duration of virus shedding was calculated in days from the first to the last dose, and the mean duration of shedding was determined for each treatment group. The placebo-vaccinated control group had a mean duration of virus shedding of 7 days. In contrast, treatment groups A and C had a mean duration of shedding of 0 days, while treatment groups B and D had a mean duration of shedding of 1 day (see Table 3 below).

[0072] Table 3 Emission period [Table 4]

[0073] These results indicate that CARBIGEN™ and PVP-K60 had little effect on the duration of CPI virus shedding in vaccinated dogs.

[0074] Example 2 CPI virus dose response of multivalent oral CPI virus and B. bronchiseptica vaccines with and without adjuvant Materials and Methods vaccine: The experimental vaccine contained avirulent live B. bronchiseptica antigen B-C2, ATCC Accession Number PTA-126272, mixed with stabilizers [hydrolyzed gelatin, NZ Amine AS, sorbitol-d, dibasic sodium phosphate] and then lyophilized, and modified live CPI virus, strain Cornell, antigen ATCC Accession Number PTA-126273. The vaccine administered to dogs in treatment groups C and D contained 15% CARBIGEN™ as an adjuvant. On the day of vaccination, each vial of lyophilized vaccine was rehydrated with 1 mL of sterile water, and similar preparations were pooled. The titers of CPI virus in the vaccines used in treatment groups A through D were 8.6, 7.3, 7.6, and 6.3 log , respectively, as shown in Table 5. 10 HAID 50 / mL.

[0075] animal: Fifteen 17-week-old beagles (Marshall Bioresources) were housed together in a BSL-2 facility on a concrete floor covered with wood shavings, with food and water available ad libitum.

[0076] Vaccination and serum collection: On study day 0, dogs were vaccinated with their individual pooled vaccine 1 mL doses by the oral route [see Table 4 below]. A spray device was attached to the syringe to deliver the vaccine to the back of the throat. On study day 27, whole blood was collected by venipuncture of the jugular vein. Serum was separated by centrifugation and stored at -10°C or below until testing.

[0077] Detection of CPI virus neutralizing antibodies: A standard SN assay was used to detect CPI virus-neutralizing antibodies. Serum dilutions were incubated with the CPI virus vaccine strain and inoculated into canine kidney cells. After 5–7 days, monolayers were fixed and stained with fluorescein-conjugated CPI virus antiserum, and SN antibody titers were calculated as the reciprocal of the serum dilution that caused 50% inhibition of virus infection.

[0078] Challenge: On study day 28, dogs were challenged with virulent CPI virus.

[0079] Post-challenge observations and samples: Clinical observations were recorded for 14 consecutive days, and nasal swabs were collected for 10 consecutive days after challenge.

[0080] Table 4 Test Design [Table 5]

[0081] result Serology: Prior to vaccination, all dogs had CPI virus serum neutralizing titers of less than 2, indicating that the dogs were virus-free at the time of vaccination. Placebo-vaccinated control dogs remained seronegative (SN<2) until immediately prior to vaccination. Nearly all dogs in each treatment group seroconverted (titers >4) after vaccination [see Table 5 below].

[0082] Table 5 Serum antibody titers against CPI virus [Table 6]

[0083] CPI viral shedding: Duration of CPI virus shedding was the primary variable for assessing vaccine efficacy. For each animal, the duration of virus shedding was calculated in days from the first to the last dose, and the mean duration of shedding was determined for each treatment group. All placebo-vaccinated control dogs (treatment group E) shed virus, with a mean duration of shedding of 6 days. In contrast, the mean durations of shedding for treatment groups A through D were 1, 0, 1, and 5, respectively (see Table 6 below).

[0084] Table 6 Emission period [Table 7]

[0085] These results, evaluated as a function of the duration of viral shedding, showed a ≥ 6.3 log 10 HAID 50 This suggests that 100% of the modified live CPI virus / mL is required for an oral modified live CPI virus vaccine to be effective.

[0086] Example 3 Immunogenicity study in dogs to demonstrate efficacy of the CPI fraction of an oral canine parainfluenza and Bordetella bronchiseptica combination vaccine Materials and Methods vaccine: The test vaccine consisted of the modified live CPI virus strain Cornell (ATCC accession number PTA-126273) and avirulent B. bronchiseptica antigen B-C2 (ATCC accession number PTA-126272), mixed with stabilizers (hydrolyzed gelatin, NZ amine AS, sorbitol-d, and dibasic sodium phosphate), and lyophilized. The placebo vaccine consisted of all components of the test vaccine except the CPI antigen. On the day of vaccination, each vial of lyophilized vaccine was rehydrated with 1 mL of sterile water, and similar preparations were pooled.

[0087] animal: Twenty 7-week-old beagles (Marshall Bioresources) were housed together in a BSL-2 facility on a concrete floor covered with wood shavings, and 19 7-week-old beagles (Marshall Bioresources) were housed similarly in a separate room with free access to food and water.

[0088] Vaccination and serum collection: On Study Day 0, dogs were vaccinated with their individual pooled vaccine 1 mL doses by the oral route [see Table 7 below]. A spray device was attached to the syringe to deliver the vaccine to the back of the oral cavity (oropharynx). On Study Day 21, whole blood was collected by venipuncture of the jugular vein. Serum was separated by centrifugation and stored at -10°C or below until testing.

[0089] Detection of CPI virus neutralizing antibodies: A standard SN assay was used to detect CPI virus-neutralizing antibodies. Serum dilutions were incubated with the CPI virus vaccine strain and inoculated into canine kidney cells. After 5–7 days, monolayers were fixed and stained with fluorescein-conjugated CPI virus antiserum, and SN antibody titers were calculated as the reciprocal of the serum dilution that caused 50% inhibition of virus infection.

[0090] Challenge: On study day 21, dogs were challenged with virulent CPI virus.

[0091] Post-challenge observations and samples: Clinical observations were recorded for 14 consecutive days, and nasal swabs were collected for 10 consecutive days after challenge.

[0092] Table 7 Test Design [Table 8]

[0093] result Serology: Prior to vaccination, all dogs had CPI virus serum neutralizing titers of less than 2, indicating that the dogs had not been infected with the virus at the time of vaccination. While vaccination with the placebo vaccine did not induce CPI-specific antibodies, vaccination with the test vaccine induced CPI serum neutralizing titers of 4 or greater in 15 of 20 vaccinated animals (75%), with titers ranging from 6 to 861 (GMT=31) 3 weeks after vaccination [see Table 8 below].

[0094] Table 8 CPI serum antibody titers [Table 9]

[0095] CPI viral shedding: Duration of CPI virus shedding was the primary variable for assessing vaccine efficacy.

[0096] The duration of virus shedding in days from the first to the last dose was calculated for each animal, and the mean duration of shedding for each treatment group was determined. All but one of the placebo-vaccinated control dogs (treatment group B) shed CPI virus (i.e., 95%), while only 11 of the vaccinated animals shed virus (i.e., 55%). The median duration of CPI virus shedding was 6 days for placebo-vaccinated control dogs, compared with only 1.5 days for vaccinated dogs (see Table 9 below).

[0097] Table 9 Emission period [Table 10]

[0098] These results, evaluated as a function of the duration of viral shedding, showed a 7.1 log 10 HAID 50 / mL of CPI virus is sufficient for an oral modified live CPI virus vaccine to be effective.

[0099] Example 4 Immunogenicity study to demonstrate efficacy of the Bordetella bronchiseptica fraction of an oral canine parainfluenza and Bordetella bronchiseptica combination vaccine Materials and Methods vaccine: The test vaccine consisted of modified live CPI virus strain Cornell (ATCC accession number PTA-126273) and avirulent B. bronchiseptica antigen B-C2 (ATCC accession number PTA-126272), mixed with stabilizers (hydrolyzed gelatin, NZ amine AS, sorbitol-d, and dibasic sodium phosphate), and lyophilized. The placebo vaccine consisted of all components of the test vaccine except the B. bronchiseptica antigen. On the day of vaccination, each vial of lyophilized vaccine was rehydrated with sterile water, and similar preparations were pooled.

[0100] animal: Twenty-one 7-week-old beagles were housed together in a BSL-2 facility on a concrete floor covered with wood shavings, and 21 7-week-old beagles were similarly housed in a separate room with free access to food and water.

[0101] Vaccination: On Study Day 0, dogs were vaccinated with their individual 1 mL doses of pooled vaccine by the oral route [see Table 10 below]. A spray device was attached to the syringe to deliver the vaccine to the back of the oral cavity (oropharynx).

[0102] Sample Collection: Whole blood was collected by venipuncture of the jugular vein on study day 34. Serum was separated by centrifugation and stored at or below -10°C until testing. Nasal swabs were also collected on study day 34 to test for the presence of B. bronchiseptica. After collection, swabs were placed in wheel pack bags and tested immediately.

[0103] Detection of B. bronchiseptica agglutinating antibodies: A standard microagglutination test was used to detect B. bronchiseptica antibodies. Two-fold serial dilutions of test serum, known positive serum, and known negative serum were performed in U-bottom microtiter plates using normal saline containing 0.1% gelatin as the diluent. B. bronchiseptica antigen (100 μL) was added to each well and mixed for 15–30 seconds on a microtiter plate mixer. Plates were incubated at 36 ± 2°C for 1–3 hours, followed by incubation at 2–7°C for 36–72 hours. Plates were read visually for agglutination, and titers were expressed as the reciprocal of the highest dilution showing complete agglutination.

[0104] Challenge: On study day 35, dogs were inoculated with virulent B. bronchiseptica.

[0105] Post-challenge observations and samples: Dogs were observed for at least 30 minutes twice daily for 28 days post-challenge for clinical signs, including but not limited to nasal discharge, dyspnea, depression, and coughing. Nasal swabs were collected on study days 42, 45, 49, 52, 58, and 63 to measure shedding of the challenged organism.

[0106] Table 10 Test Design [Table 11]

[0107] result Serology: Prior to vaccination, all dogs had low antibody titers (≤4) to B. bronchiseptica, indicating that the dogs had not been infected with the virus at the time of vaccination. Administration of the study vaccine induced B. bronchiseptica agglutination titers in 20 of 21 dogs, ranging from 16 to 128 on study day 34; GMT = <39. In contrast, antibody titers in placebo-vaccinated control dogs remained low, ranging from <2 to 8, with GMT = <1 [see Table 11 below].

[0108] Table 11 B. bronchiseptica serum antibody titers [Table 12]

[0109] Clinical signs after challenge: After challenge, all placebo-vaccinated control dogs developed clinical signs associated with B. bronchiseptica infection, particularly spontaneous coughing. Affected dogs were defined as having spontaneous coughing or spontaneous coughing accompanied by vomiting on two or more consecutive days during the post-challenge observation period. All 20 placebo-vaccinated control dogs were affected, whereas only 9 of 21 vaccinated control dogs (43%) were affected; p < 0.0001 [see Table 12 below]. Furthermore, while no vaccinated dogs coughed more than once on two consecutive days during the post-challenge observation period, 18 of 20 placebo-vaccinated control dogs (90%) coughed 2 to 13 times on two consecutive days.

[0110] Table 12 Summary of affected dogs [Table 13]

[0111] The number of days the dogs spontaneously coughed during the 28-day post-treatment observation period was also analyzed. Dogs in treatment group B had a mean of 16.6 days with spontaneous coughing, compared with only 3.5 days for dogs in treatment group A; p-value <0.0001 [see Table 13 below].

[0112] Table 13 Summary of coughs [Table 14]

[0113] B. bronchiseptica shedding: Nasal swabs were collected twice weekly for 4 weeks after administration to measure shedding of the administered microorganism. There was no difference in shedding between the placebo-vaccinated and vaccine groups on study day 42. However, by study day 45, the placebo-vaccinated control group shed 38,141 cfu / mL of B. bronchiseptica, while the vaccine group shed only 1,523 cfu / mL. Shedding in the placebo-vaccinated control group peaked at 75,293 cfu / mL on day 16 after inoculation (study day 52). In contrast, shedding in the vaccine group peaked at 4,173 cfu / mL on day 6 after inoculation (study day 42). Bacterial counts continued to decrease in the vaccine group until the end of the study. By study day 63, bacterial shedding in the vaccinated group was only 6 cfu / mL, while within the placebo control group, shedding remained high at 35,400 cfu / mL.

[0114] These data demonstrate a significant reduction in the ability of B. bronchiseptica to colonize the nasal mucosa in the vaccinated group. Overall mean bacterial shedding for the placebo-vaccinated control and vaccinated groups was 37,035 cfu / mL and 849 cfu / mL, respectively (see Table 14 below), and the amount of B. bronchiseptica shed on each collection day was statistically lower in the vaccinated group than in the placebo-vaccinated control group (p-value ≦0.0001).

[0115] Table 14 Bronchiseptica isolates from post-administration nasal swabs (cfu / mL) [Table 15]

[0116] These results were assessed by the number of dogs that had spontaneous cough or spontaneous cough with retching for 2 or more consecutive days during the post-dose observation period, with a mean of 3.9 × 10 per 1 mL dose. 8 cfu / mL of the avirulent B. bronchiseptica strain B-C2, ATCC Accession Number PTA-126272, is sufficient for the oral vaccine to be effective.

[0117] The present invention is not limited in scope by the specific embodiments described herein. Indeed, various modifications of the invention in addition to those described herein will become apparent to those skilled in the art from the foregoing description. Such modifications are intended to fall within the scope of the appended claims.

Claims

1. 1. A method for providing effective protection against upper respiratory tract disease and infectious tracheobronchitis to a dog, comprising orally administering to the dog a single dose of a bivalent vaccine comprising a modified live canine parainfluenza (CPI) virus and a live avirulent Bordetella bronchiseptica (B. bronchiseptica), wherein: The method wherein the modified live CPI virus is administered at a titer of 6.0 log 10 HAID 50 / dose or greater, and wherein administration protects the dog from upper respiratory tract disease and infectious tracheobronchitis.

2. The titer of the administered non-toxic live B. bronchiseptica is 1 x 10 ７ 10. The method of claim 1, wherein the immunization dose is greater than or equal to 1000 cfu / dose.

3. (i) the titer of the administered modified live CPI virus is 6.8 log １０ H.A.I.D. ５０ / dose~9.5 log １０ H.A.I.D. ５０ / dose, (ii) the titer of the administered non-toxic live B. bronchiseptica is 1 x 10 ８ cfu / dose~1×10 １２ cfu / dose, or (iii) the titer of the administered modified live CPI virus is 6.8 log １０ H.A.I.D. ５０ / dose~9.5 log １０ H.A.I.D. ５０ / dose, and the titer of the administered non-toxic live B. bronchiseptica is 1 x 10 ８ cfu / dose~1×10 １２ cfu / dose, The method of claim 1.

4. 4. The method of any one of claims 1 to 3, wherein the modified live CPI virus has ATCC accession number PTA-126273.

5. 5. The method of any one of claims 1 to 4, wherein the live avirulent B. bronchiseptica has ATCC Accession No. PTA-126272.

6. The method of any one of claims 1 to 5, wherein the bivalent vaccine is a non-adjuvanted vaccine.

7. The method of any one of claims 1 to 5, wherein the bivalent vaccine further comprises an adjuvant.

8. 1. An oral vaccine for providing effective protection against upper respiratory tract disease and infectious tracheobronchitis to dogs by oral administration, comprising: Here, the oral vaccine has a 6.0 log １０ H.A.I.D. ５０ 1. A bivalent oral vaccine comprising a titer of modified live canine parainfluenza (CPI) virus of 1 x 10 cfu / mL or greater and a titer of avirulent live Bordetella bronchiseptica (B. bronchiseptica) of 1 x 10 cfu / dose or greater, and wherein said oral vaccine is for single dose administration.

9. The titer of the avirulent live B. bronchiseptica in the vaccine is 1 x 10 ７ cfu / mL~1×10 １２ The oral vaccine of claim 8, wherein the IgG antibody concentration is 1000 mg / mL.

10. The titer of the modified live CPI virus in the vaccine is 6.0 log １０ H.A.I.D. ５０ / mL ~ 9.5 log １０ H.A.I.D. ５０ The oral vaccine of claim 8 or 9, wherein the oral vaccine is administered in an amount of 1000 mg / mL.

11. The oral vaccine of any one of claims 8 to 10, wherein the modified live CPI virus has ATCC accession number PTA-126273.

12. 12. The oral vaccine of any one of claims 8 to 11, wherein the live avirulent B. bronchiseptica has ATCC accession number PTA-126272.

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