Boggiatto Paola M, Sterle Haley, Falkenberg Shollie, Sarlo-Davila Kaitlyn, Putz Ellie J, Olsen Steven C
Infectious Bacterial Diseases Research Unit, National Animal Disease Center, Ames, IA, United States.
Immunobiology Interdepartmental Program, Iowa State University, Ames, IA, United States.
Front Vet Sci. 2024 Jul 26;11:1367498. doi: 10.3389/fvets.2024.1367498. eCollection 2024.
strain RB51 is the commercial cattle vaccine used in the United States (US) and many parts of the world against bovine brucellosis. RB51 was licensed for use in 1996, and it has been shown to be safe and efficacious in cattle, eliciting humoral and cellular responses in calves and adult animals. In 2017, an epidemiological trace-back investigation performed by the Centers for Disease Control and Prevention (CDC) identified human cases of brucellosis caused by infection with RB51. These infections resulted from the consumption of unpasteurized dairy products, which were traced back to otherwise healthy animals that were shedding RB51 in their milk. At the current time, six adult Jersey cows have been identified in the U.S. that are shedding RB51 in milk. One of the RB51 shedding cattle was obtained and housed at the National Animal Disease Center (NADC) for further study. Improved understanding of host cellular and humoral immune responses to RB51 in persistently colonized cattle may be achieved by the characterization of responses in shedding animals. We hypothesized, based on the lack of RB51 clearance, that the RB51 shedder animal has a diminished adaptive cellular immune response to RB51. Our data demonstrate that in the presence of persistent RB51 infection, there is a lack of peripheral anti-RB51 CD4 T cell responses and a concurrently high anti-RB51 IgG humoral response. By understanding the mechanisms that result in RB51 persistence, the development of improved interventions or vaccinations for brucellosis may be facilitated, which would provide public health benefits, including reducing the risks associated with the consumption of non-pasteurized milk products.
RB51菌株是美国及世界许多地区用于预防牛布鲁氏菌病的商用牛疫苗。RB51于1996年获得使用许可,已证明其在牛身上安全有效,能在犊牛和成年动物中引发体液免疫和细胞免疫反应。2017年,美国疾病控制与预防中心(CDC)进行的一项流行病学追溯调查发现了由RB51感染引起的人类布鲁氏菌病病例。这些感染是由于食用了未经过巴氏杀菌的乳制品,这些乳制品可追溯到在牛奶中排出RB51的健康动物。目前,在美国已确定有6头成年泽西奶牛在牛奶中排出RB51。其中一头排出RB51的奶牛被带到国家动物疾病中心(NADC)饲养以进行进一步研究。通过对排菌动物的反应进行表征,可能会更好地了解持续定植牛对RB51的宿主细胞免疫和体液免疫反应。基于RB51未被清除,我们推测排菌动物对RB51的适应性细胞免疫反应减弱。我们的数据表明,在持续存在RB51感染的情况下,外周血中缺乏抗RB51 CD4 T细胞反应,同时抗RB51 IgG体液反应较高。通过了解导致RB51持续存在的机制,可能会促进开发改进的布鲁氏菌病干预措施或疫苗,这将带来公共卫生益处,包括降低与食用未巴氏杀菌奶制品相关的风险。