Circulating T cell subpopulations in dairy calves infected with Bovine viral diarrhea virus 2 and Bovine herpes virus 1 following modified-live virus booster vaccination: Effects of the administration route and trace mineral supplementation

IF 1.4 3区 农林科学 Q4 IMMUNOLOGY Veterinary immunology and immunopathology Pub Date : 2025-02-01 DOI:10.1016/j.vetimm.2024.110871
A. Hoyos-Jaramillo , R.A. Palomares , J.H.J. Bittar , D.J. Hurley , A. Rodríguez , E.A. González-Altamiranda , S. Kirks , A. Gutierrez , S. Wall , K. Miller , J. Urdaneta , K. Skrada , D. Lopez , M. Fenley
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Abstract

The objective of this study was to evaluate the effects of the vaccine administration route and the concurrent use of injectable trace minerals (ITM) with booster vaccination on the circulating leukocyte counts and T cell subpopulations in dairy calves challenged with Bovine viral diarrhea virus 2 (BVDV2) and Bovine herpes virus 1 (BHV1). A total of 60 Holstein male calves were used in this study. Forty-eight calves were administered a MLV intranasal (IN) vaccine containing BHV1, BRSV, BPI3V (Inforce 3®), and randomly assigned to subcutaneous (SC) administration of injectable trace minerals (ITM, n = 24) or saline (SAL, n = 24). Ten weeks later, the calves received booster vaccination using either SC or IN route and a second dose of ITM, or saline, according to previous groups [ITM-SC (n = 12), ITM-IN (n = 12), SAL-SC (n = 12), and SAL-IN (n = 12)]. Additionally, 12 calves did not receive vaccine or treatment (UNVAC, n = 12). Seven weeks after booster all calves were challenged with BVDV2 and seven days later with BHV1. Blood samples were collected on days −7, 0, 3, 6, 7, 10, 12 and 14 for determination of leukocyte counts and T cell subpopulations (CD4+, CD8+, WC1+ and CD25+). Unvaccinated calves had a significant leukopenia, compared to the vaccinated calves. There was a significant decrease of CD4+ CD8+ T cells over time after BVDV2 challenge, being more pronounced in the UNVAC calves. Calves receiving SC vaccination appeared to have greater CD4+ T cell number compared to the UNVAC calves. Calves treated with ITM had greater CD8+ T cells count than the other groups. Calves in the ITM-IN group had the greatest CD8+ T cell count on days 6 and 7 (P < 0.01). All vaccinated groups had steady response of CD4+CD25+ T cells and a slight increase of CD8+CD25+ T cells. In contrast, UNVAC calves had a significant increase of CD4+CD25+, CD8+CD25+ and WC1+CD25+ T cells on day 14. In conclusion, vaccine administration route and use of injectable trace minerals concurrent with vaccination affected the number CD4+ and CD8+ T cells in response to BVDV2 +BHV1 infection. Trace minerals supplementation concurrent with MLV vaccination might generate an improved cellular immunity against viral infections involved in respiratory disease.
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改良活病毒增强疫苗接种后感染牛病毒性腹泻病毒2型和牛疱疹病毒1型的犊牛循环T细胞亚群:给药途径和微量矿物质补充的影响
本研究的目的是评估疫苗接种途径和同时使用可注射微量矿物质(ITM)与加强疫苗接种对牛病毒性腹泻病毒2 (BVDV2)和牛疱疹病毒1 (BHV1)攻毒的奶牛循环白细胞计数和T细胞亚群的影响。本研究共选用60头荷斯坦公犊牛。48头小牛接种了含有BHV1、BRSV、BPI3V (Inforce 3®)的MLV鼻内疫苗(IN),并随机分配到皮下注射微量矿物质(ITM, n = 24)或生理盐水(SAL, n = 24)。十周后,根据先前的组[ITM-SC (n = 12),ITM-IN (n = 12),SAL-SC (n = 12)和SAL-IN (n = 12)],小牛接受SC或IN途径的加强疫苗接种和第二剂ITM或生理盐水。此外,12头小牛没有接受疫苗或治疗(UNVAC, n = 12)。增强后7周,所有犊牛接种BVDV2, 7天后接种BHV1。于第-7、0、3、6、7、10、12和14天采集血样,测定白细胞计数和T细胞亚群(CD4+、CD8+、WC1+和CD25+)。与接种疫苗的小牛相比,未接种疫苗的小牛有明显的白细胞减少。在BVDV2攻击后,CD4+ CD8+ T细胞随着时间的推移显着减少,在UNVAC小牛中更为明显。与UNVAC小牛相比,接受SC疫苗接种的小牛似乎有更多的CD4+ T细胞数量。与其他组相比,经ITM处理的小牛CD8+ T细胞计数更高。ITM-IN组犊牛在第6天和第7天CD8+ T细胞计数最高(P +CD25+ T细胞),CD8+CD25+ T细胞计数略有增加。相比之下,UNVAC犊牛在第14天CD4+CD25+、CD8+CD25+和WC1+CD25+ T细胞显著增加。综上所述,疫苗给药途径和注射微量矿物质同时接种影响了BVDV2 +BHV1感染后CD4+和CD8+ T细胞的数量。微量矿物质补充与MLV疫苗接种可能产生改善的细胞免疫系统,以对抗呼吸道疾病的病毒感染。
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来源期刊
CiteScore
3.40
自引率
5.60%
发文量
79
审稿时长
70 days
期刊介绍: The journal reports basic, comparative and clinical immunology as they pertain to the animal species designated here: livestock, poultry, and fish species that are major food animals and companion animals such as cats, dogs, horses and camels, and wildlife species that act as reservoirs for food, companion or human infectious diseases, or as models for human disease. Rodent models of infectious diseases that are of importance in the animal species indicated above,when the disease requires a level of containment that is not readily available for larger animal experimentation (ABSL3), will be considered. Papers on rabbits, lizards, guinea pigs, badgers, armadillos, elephants, antelope, and buffalo will be reviewed if the research advances our fundamental understanding of immunology, or if they act as a reservoir of infectious disease for the primary animal species designated above, or for humans. Manuscripts employing other species will be reviewed if justified as fitting into the categories above. The following topics are appropriate: biology of cells and mechanisms of the immune system, immunochemistry, immunodeficiencies, immunodiagnosis, immunogenetics, immunopathology, immunology of infectious disease and tumors, immunoprophylaxis including vaccine development and delivery, immunological aspects of pregnancy including passive immunity, autoimmuity, neuroimmunology, and transplanatation immunology. Manuscripts that describe new genes and development of tools such as monoclonal antibodies are also of interest when part of a larger biological study. Studies employing extracts or constituents (plant extracts, feed additives or microbiome) must be sufficiently defined to be reproduced in other laboratories and also provide evidence for possible mechanisms and not simply show an effect on the immune system.
期刊最新文献
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