Randomized controlled trial comparing the immunogenicity of experimental Salmonella Dublin siderophore receptor vaccines in calves.

IF 1.3 3区 农林科学 Q2 VETERINARY SCIENCES American journal of veterinary research Pub Date : 2025-01-07 DOI:10.2460/ajvr.24.08.0215
Kristen P Hayman, Cody Sacquitne, Angela D Rowson, Doug T Burkhardt, Mark P Peterson, Darren E Straub, Jodi L McGill, Patrick J Gorden
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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.

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比较实验性都柏林铁载体沙门氏菌受体疫苗对犊牛免疫原性的随机对照试验。
目的:描述实验性都柏林铁载体受体蛋白(SRP)疫苗对荷斯坦小母牛犊牛的免疫反应,并进行充分的被动抗体转移。方法:犊牛在7±3日龄和3周后随机分为安慰剂组,接种S都柏林SRP佐剂A组,或接种S都柏林SRP佐剂B组。分别在每次接种前、第二次接种后第4天和第8天(接种后)以及接种后61 ~ 91天测定S Dublin抗体滴度。接种疫苗后4和8天采集的血液中分离的血单个核细胞,分别用S Dublin SRP抗原(1或5µg/mL)或阳性或阴性对照刺激,然后定量分析S Dublin SRP应答细胞。同样刺激血单核细胞培养以量化产生干扰素-γ (IFN-γ)和产生il -17的细胞。试验时间为2022年9月4日至2023年1月15日。结果:78头小牛入组。除1 μ g/mL刺激后第4天IFN-γ浓度升高外,接种疫苗后第4天产生IFN-γ的细胞和IFN-γ和IL-17浓度均显著升高。接种者在接种后8天和61至90天也有较高的S都柏林滴度。没有注意到健康事件的差异。结论:接种疫苗可诱导荷斯坦小母牛犊牛产生S Dublin srp特异性体液和细胞免疫反应。临床相关性:接种SRP疫苗可产生免疫反应,可能有助于减轻都柏林S感染。需要进一步的研究来确定疫苗接种是否能够预防都柏林病毒的挑战。
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来源期刊
CiteScore
1.70
自引率
10.00%
发文量
186
审稿时长
3 months
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.
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