ArticleVirulence2026
Immunogenicity evaluation of recombinant rabies virus-vectored multivalent vaccines expressing feline calicivirus VP1 and feline herpesvirus 1 gB/gD genes.
Article in Virulence, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.
What it found
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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
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Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.
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Who cites it
1 citing paper in PubMed.
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Authors and funding
13 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Feline calicivirus (FCV) and feline herpesvirus 1 (FHV-1) are major pathogens threatening feline health, and prophylactic immunity remains the primary preventive approach. To develop a safe and effective multivalent vaccine against the two viruses, two recombinant rabies virus (RABV) vaccines expressing the FCV VP1 and FHV-1 gB/gD genes were constructed. The exogenous genes showed stable inheritance following serial viral passages, and the recombinant RABVs exhibited growth kinetics comparable to the parental strain, with a delayed peak titer. After verifying the viral pathogenicity, the recombinant RABV vaccines elicited specific IgG antibodies against VP1, gB, and gD, as well as neutralizing antibodies against FCV, FHV-1, and RABV in mice. Immunized mice were also protected against lethal RABV challenge. In cats, the vaccines induced neutralizing antibodies against the three pathogens, and immunized cats showed milder clinical signs and less severe histopathological lesions following FHV-1 and FCV challenge. Collectively, these findings indicate that the two recombinant vaccines induce robust humoral immune responses against FCV, FHV-1, and RABV in both mice and cats and confer protection against viral challenges.
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