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
{"title":"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","authors":"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","doi":"10.1016/j.vetimm.2024.110871","DOIUrl":null,"url":null,"abstract":"<div><div>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 <em>Bovine viral diarrhea virus 2</em> (BVDV2) and <em>Bovine herpes virus 1</em> (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<sup>+</sup>, CD8<sup>+</sup>, WC1<sup>+</sup> and CD25<sup>+</sup>). Unvaccinated calves had a significant leukopenia, compared to the vaccinated calves. There was a significant decrease of CD4<sup>+</sup> CD8<sup>+</sup> T cells over time after BVDV2 challenge, being more pronounced in the UNVAC calves. Calves receiving SC vaccination appeared to have greater CD4<sup>+</sup> T cell number compared to the UNVAC calves. Calves treated with ITM had greater CD8<sup>+</sup> T cells count than the other groups. Calves in the ITM-IN group had the greatest CD8<sup>+</sup> T cell count on days 6 and 7 (P < 0.01). All vaccinated groups had steady response of CD4<sup>+</sup>CD25<sup>+</sup> T cells and a slight increase of CD8<sup>+</sup>CD25<sup>+</sup> T cells. In contrast, UNVAC calves had a significant increase of CD4<sup>+</sup>CD25<sup>+</sup>, CD8<sup>+</sup>CD25<sup>+</sup> and WC1<sup>+</sup>CD25<sup>+</sup> T cells on day 14. In conclusion, vaccine administration route and use of injectable trace minerals concurrent with vaccination affected the number CD4<sup>+</sup> and CD8<sup>+</sup> 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.</div></div>","PeriodicalId":23511,"journal":{"name":"Veterinary immunology and immunopathology","volume":"280 ","pages":"Article 110871"},"PeriodicalIF":1.4000,"publicationDate":"2025-02-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"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\",\"authors\":\"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\",\"doi\":\"10.1016/j.vetimm.2024.110871\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><div>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 <em>Bovine viral diarrhea virus 2</em> (BVDV2) and <em>Bovine herpes virus 1</em> (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<sup>+</sup>, CD8<sup>+</sup>, WC1<sup>+</sup> and CD25<sup>+</sup>). Unvaccinated calves had a significant leukopenia, compared to the vaccinated calves. There was a significant decrease of CD4<sup>+</sup> CD8<sup>+</sup> T cells over time after BVDV2 challenge, being more pronounced in the UNVAC calves. Calves receiving SC vaccination appeared to have greater CD4<sup>+</sup> T cell number compared to the UNVAC calves. Calves treated with ITM had greater CD8<sup>+</sup> T cells count than the other groups. Calves in the ITM-IN group had the greatest CD8<sup>+</sup> T cell count on days 6 and 7 (P < 0.01). All vaccinated groups had steady response of CD4<sup>+</sup>CD25<sup>+</sup> T cells and a slight increase of CD8<sup>+</sup>CD25<sup>+</sup> T cells. In contrast, UNVAC calves had a significant increase of CD4<sup>+</sup>CD25<sup>+</sup>, CD8<sup>+</sup>CD25<sup>+</sup> and WC1<sup>+</sup>CD25<sup>+</sup> T cells on day 14. In conclusion, vaccine administration route and use of injectable trace minerals concurrent with vaccination affected the number CD4<sup>+</sup> and CD8<sup>+</sup> 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.</div></div>\",\"PeriodicalId\":23511,\"journal\":{\"name\":\"Veterinary immunology and immunopathology\",\"volume\":\"280 \",\"pages\":\"Article 110871\"},\"PeriodicalIF\":1.4000,\"publicationDate\":\"2025-02-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Veterinary immunology and immunopathology\",\"FirstCategoryId\":\"97\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S0165242724001570\",\"RegionNum\":3,\"RegionCategory\":\"农林科学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q4\",\"JCRName\":\"IMMUNOLOGY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Veterinary immunology and immunopathology","FirstCategoryId":"97","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S0165242724001570","RegionNum":3,"RegionCategory":"农林科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q4","JCRName":"IMMUNOLOGY","Score":null,"Total":0}
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
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.
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.