Kristen P Hayman, Cody Sacquitne, Angela D Rowson, Doug T Burkhardt, Mark P Peterson, Darren E Straub, Jodi L McGill, Patrick J Gorden
{"title":"Randomized controlled trial comparing the immunogenicity of experimental Salmonella Dublin siderophore receptor vaccines in calves.","authors":"Kristen P Hayman, Cody Sacquitne, Angela D Rowson, Doug T Burkhardt, Mark P Peterson, Darren E Straub, Jodi L McGill, Patrick J Gorden","doi":"10.2460/ajvr.24.08.0215","DOIUrl":null,"url":null,"abstract":"<p><strong>Objective: </strong>To describe immune responses following administration of experimental Salmonella Dublin siderophore receptor protein (SRP) vaccines in Holstein heifer calves with adequate passive antibody transfer.</p><p><strong>Methods: </strong>Calves were randomly assigned to receive placebo, vaccination with S Dublin SRP in adjuvant A, or vaccination with S Dublin SRP in adjuvant B at 7 ± 3 days of age and 3 weeks later. Before each vaccination, 4 and 8 days after the second vaccination (postvaccination), and 61 to 91 days postvaccination, S Dublin antibody titers were measured. Blood mononuclear cells isolated from blood collected 4 and 8 days postvaccination were stimulated with S Dublin SRP antigen (1 or 5 µg/mL) or positive or negative controls, then analyzed to quantify S Dublin SRP-responsive cells. Cultures of blood mononuclear cells were similarly stimulated to quantify interferon-γ (IFN-γ)-producing and IL-17-producing cells. The trial spanned September 4, 2022, through January 15, 2023.</p><p><strong>Results: </strong>78 calves were enrolled. Vaccinates had significantly higher IFN-γ-producing cells and IFN-γ and IL-17 concentrations at 4 and 8 days postvaccination, except IFN-γ concentration at day 4 after stimulation with 1 µg/mL. Vaccinates also had higher S Dublin titers at 8 and 61 to 90 days postvaccination. No differences in health events were noted.</p><p><strong>Conclusions: </strong>Vaccination can induce S Dublin SRP-specific humoral and cellular immune responses in Holstein heifer calves.</p><p><strong>Clinical relevance: </strong>Vaccination with SRP vaccines resulted in immune responses that may help mitigate S Dublin infection. Further research is needed to determine whether vaccination will be protective against S Dublin challenge.</p>","PeriodicalId":7754,"journal":{"name":"American journal of veterinary research","volume":" ","pages":"1-8"},"PeriodicalIF":1.3000,"publicationDate":"2025-01-07","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"American journal of veterinary research","FirstCategoryId":"97","ListUrlMain":"https://doi.org/10.2460/ajvr.24.08.0215","RegionNum":3,"RegionCategory":"农林科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"VETERINARY SCIENCES","Score":null,"Total":0}
引用次数: 0
Abstract
Objective: To describe immune responses following administration of experimental Salmonella Dublin siderophore receptor protein (SRP) vaccines in Holstein heifer calves with adequate passive antibody transfer.
Methods: Calves were randomly assigned to receive placebo, vaccination with S Dublin SRP in adjuvant A, or vaccination with S Dublin SRP in adjuvant B at 7 ± 3 days of age and 3 weeks later. Before each vaccination, 4 and 8 days after the second vaccination (postvaccination), and 61 to 91 days postvaccination, S Dublin antibody titers were measured. Blood mononuclear cells isolated from blood collected 4 and 8 days postvaccination were stimulated with S Dublin SRP antigen (1 or 5 µg/mL) or positive or negative controls, then analyzed to quantify S Dublin SRP-responsive cells. Cultures of blood mononuclear cells were similarly stimulated to quantify interferon-γ (IFN-γ)-producing and IL-17-producing cells. The trial spanned September 4, 2022, through January 15, 2023.
Results: 78 calves were enrolled. Vaccinates had significantly higher IFN-γ-producing cells and IFN-γ and IL-17 concentrations at 4 and 8 days postvaccination, except IFN-γ concentration at day 4 after stimulation with 1 µg/mL. Vaccinates also had higher S Dublin titers at 8 and 61 to 90 days postvaccination. No differences in health events were noted.
Conclusions: Vaccination can induce S Dublin SRP-specific humoral and cellular immune responses in Holstein heifer calves.
Clinical relevance: Vaccination with SRP vaccines resulted in immune responses that may help mitigate S Dublin infection. Further research is needed to determine whether vaccination will be protective against S Dublin challenge.
期刊介绍:
The American Journal of Veterinary Research supports the collaborative exchange of information between researchers and clinicians by publishing novel research findings that bridge the gulf between basic research and clinical practice or that help to translate laboratory research and preclinical studies to the development of clinical trials and clinical practice. The journal welcomes submission of high-quality original studies and review articles in a wide range of scientific fields, including anatomy, anesthesiology, animal welfare, behavior, epidemiology, genetics, heredity, infectious disease, molecular biology, oncology, pharmacology, pathogenic mechanisms, physiology, surgery, theriogenology, toxicology, and vaccinology. Species of interest include production animals, companion animals, equids, exotic animals, birds, reptiles, and wild and marine animals. Reports of laboratory animal studies and studies involving the use of animals as experimental models of human diseases are considered only when the study results are of demonstrable benefit to the species used in the research or to another species of veterinary interest. Other fields of interest or animals species are not necessarily excluded from consideration, but such reports must focus on novel research findings. Submitted papers must make an original and substantial contribution to the veterinary medicine knowledge base; preliminary studies are not appropriate.