ArticleJournal of immunology research2026
Attenuated Infectious Bronchitis Virus (IBV) Vaccination Induces Protective Humoral and Cellular Immunity Against SARS-CoV-2 in Mammals.
Article in Journal of immunology research, 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
Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.
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.
The trial behind it
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.
- Attenuated Infectious Bronchitis Virus (IBV) Vaccination Induces Protective Humoral and Cellular Immunity Against SARS-CoV-2 in Mammals.Journal of immunology research · 2026Article
Corrections and comments
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Authors and funding
20 authors.
Funding
Abstract
Occupational exposure to infectious bronchitis virus (IBV) has been associated with cross-reactivity to other coronaviruses such as SARS-CoV-2. In this study, we investigated the immune response of IBV using reconstituted samples of the commercial H120 Mass-I vaccine (Zoetis) against SARS-CoV-2 infection. Bioinformatics analyses, serological assays, and neutralization tests were conducted to evaluate the neutralizing capacity of anti-IBV antibodies against SARS-CoV-2 in serum samples from poultry farm workers exposed to the IBV-H120 vaccine. Mouse immunization assays and flow cytometry analysis were conducted to characterize the immune response triggered by IBV-H120. Finally, a histological analysis of the lungs of Syrian hamsters vaccinated with IBV and challenged with SARS-CoV-2 (Wuhan and Delta strains) was conducted to evaluate the protective potential of the vaccine. Neutralizing antibodies against IBV-H120 were detected in the serum of poultry farm workers, indicating cross-reactivity with SARS-CoV-2. The immune response in mice immunized with IBV-H120 demonstrated that only the intranasal and oral routes were effective against SARS-CoV-2. An increase in the percentage of CD19
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Registered trials
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