Peer-reviewed veterinary case report
Dog vaccine for parvovirus type 2b also protects against types 2a
By Wilson, Stephen et al.·Published in Vaccine·2014·Zoetis·View original on PubMed →
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Original publication title: Vaccination of dogs with canine parvovirus type 2b (CPV-2b) induces neutralising antibody responses to CPV-2a and CPV-2c.
- Species:
- dog
Plain-English summary
A group of puppies was vaccinated with a new vaccine that protects against canine parvovirus type 2b (CPV-2b) to see if it would also help against other variants of the virus, CPV-2a and CPV-2c. The puppies received two vaccinations three weeks apart and showed strong antibody responses to all three variants, indicating good protection. Even after a year, their immune response remained robust, suggesting that this vaccine could effectively protect against currently circulating strains of parvovirus. This means that vaccinating your puppy with this vaccine can help keep them safe from serious illness caused by these parvovirus strains.
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Abstract
Since the identification of canine parvovirus type 2, three variants have subsequently been observed differing from the historical CPV-2 and each other by 1-2 amino acids only. As a result there has been considerable research into differential diagnostics, with some researchers indicating there is a need for new vaccines containing different strains of CPV-2. In this study we investigated whether vaccination with a CPV-2b containing vaccine would induce cross-reactive antibody responses to the other CPV-2 variants. Two studies where dogs were vaccinated with a multivalent vaccine, subsequently challenged with CPV-2b and sera samples analysed are presented. Six week old pups with defined serological status were vaccinated twice, three weeks apart and challenged either 5 weeks (MDA override study) or one year after vaccination (duration of immunity study). Sera samples were collected before each vaccination and at periods throughout each study. In each study the antibody profiles were very similar; serological responses against CPV-2a, CPV-2b and CPV-2c were higher than those for CPV-2. Nevertheless, responses against CPV-2 were well above levels considered clinically protective. In each study dogs also showed a rapid increase in antibody titres following vaccination, reached a plateau following second vaccination with a slight decline to challenge after which rapid anamnestic responses were seen. Evaluation of the serological responses suggests vaccination with CPV-2b would cross-protect against CPV-2a and CPV-2c, as well as against CPV-2 which is now extinct in the field. In conclusion we have demonstrated that vaccination of minimum aged dogs with a multivalent vaccine containing the CPV-2b variant strain will induce serological responses which are cross-reactive against all currently circulating field strains, CPV-2a and CPV-2c, and the now extinct field strain CPV-2.
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Search related cases →Original publication on PubMed: https://pubmed.ncbi.nlm.nih.gov/25148778/