Peer-reviewed veterinary case report
Safety and effectiveness of new feline herpesvirus vaccines in cats
By Lee, Yao et al.·Published in Viruses·2021·Department of Pathobiology and Diagnostic Investigation, United States·View original on PubMed →
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Original publication title: Safety and Efficacy of Felid Herpesvirus-1 Deletion Mutants in Cats.
- Species:
- cat
Plain-English summary
A group of cats was vaccinated with a new type of herpesvirus vaccine designed to improve protection against felid herpesvirus-1 (FeHV-1), which can cause serious respiratory and eye problems. After receiving the vaccine, these cats showed fewer signs of illness and less viral shedding compared to those given a standard vaccine. The new vaccine also helped the cats produce antibodies and other immune responses that could better fight off the virus. Overall, the study suggests that these new vaccines could be a safer and more effective option for preventing FeHV-1 infections in cats.
People also search for: cat herpesvirus vaccine · cat respiratory infection treatment · feline herpes symptoms and treatment
Abstract
Felid herpesvirus-1 (FeHV-1) is an important respiratory and ocular pathogen of cats and current vaccines are limited in duration and efficacy because they do not prevent infection, viral nasal shedding and latency. To address these shortcomings, we have constructed FeHV-1 gE-TK- and FeHV-1 PK- deletion mutants (gE-TK- and PK-) using bacterial artificial chromosome (BAC) mutagenesis and shown safety and immunogenicity in vitro. Here, we compare the safety and efficacy of a prime boost FeHV-1 gE-TK- and FeHV-1 PK- vaccination regimen with commercial vaccination in cats. Cats in the vaccination groups were vaccinated at 3-week intervals and all cats were challenge infected 3 weeks after the last vaccination. Evaluations included clinical signs, nasal shedding, virus neutralizing antibodies (VN), cytokine mRNA gene expression, post-mortem histology and detection of latency establishment. Vaccination with gE-TK- and PK- mutants was safe and resulted in significantly reduced clinical disease scores, pathological changes, viral nasal shedding, and viral DNA in the trigeminal ganglia (the site of latency) following infection. Both mutants induced VN antibodies and interferons after immunization. In addition, after challenge infection, we observed a reduction of IL-1β expression, and modulation of TNFα, TGFβ and IL10 expression. In conclusion, this study shows the merits of using FeHV-1 deletion mutants for prevention of FeHV-1 infection in cats.
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Search related cases →Original publication on PubMed: https://pubmed.ncbi.nlm.nih.gov/33499363/