牛传染性副结核病口服活疫苗的免疫原性和效力。
Immunogenicity and efficacy of an oral live-attenuated vaccine for bovine Johne's disease.
机构信息
Faculty of Veterinary Medicine, University of Calgary, Calgary, AB, Canada.
Vaccine and Infectious Disease Organization (VIDO), University of Saskatchewan, Saskatoon, SK, Canada.
出版信息
Front Immunol. 2024 Jan 12;14:1307621. doi: 10.3389/fimmu.2023.1307621. eCollection 2023.
subsp. (MAP), the etiological agent of Johne's disease (JD) in ruminants, establishes a prolonged and often lifelong enteric infection. The implementation of control measures for bovine JD has faced obstacles due to the considerable expenses involved in disease surveillance and hindered by unreliable and inadequate diagnostic tests, emphasizing the need for an effective vaccine that can stimulate mucosal immunity in the gastrointestinal tract. Previous investigations have demonstrated that deletion of the gene in MAP produces an attenuated strain that can transiently colonize the calf small intestine while retaining its capacity to stimulate systemic immune responses similar to wildtype MAP strains. This study assessed the efficacy of the gene deletion MAP strain, referred to as the vaccine, when administered orally to young calves. The research aimed to evaluate its effectiveness in controlling MAP intestinal infection and to investigate the immune responses elicited by mucosal vaccination. The study represents the first evaluation of an enteric modified live MAP vaccine in the context of an oral MAP challenge in young calves. Oral immunization with reduced MAP colonization specifically in the ileum and ileocecal valve. This partially protective immune response was associated with an increased frequency of CD4+ and CD8+ T cells with a pro-inflammatory phenotype (IFNγ+/TNFα+) in vaccinated animals. Moreover, re-stimulated PBMCs from vaccinated animals showed increased expression of , , , and at 10- and 12-weeks post challenge. Furthermore, immunophenotyping of blood leukocytes revealed that vaccinated calves had increased levels of T cells expressing cell-surface markers consistent with long-term central memory. Overall, our findings provide new insights into the development and immunogenicity of a modified live MAP vaccine against bovine JD, demonstrating oral vaccination can stimulate host immune responses that can be protective against enteric MAP infection.
亚种。(MAP),反刍动物的约翰氏病(JD)的病原体,建立了一个长期的,往往终身肠感染。由于疾病监测涉及相当大的费用以及不可靠和不充分的诊断测试的阻碍,牛 JD 的控制措施的实施面临障碍,强调需要一种有效的疫苗,可以刺激胃肠道的粘膜免疫。先前的研究表明,在 MAP 中删除基因会产生一种减毒菌株,该菌株可以短暂地定植小牛小肠,同时保留其刺激类似于野生型 MAP 菌株的全身免疫反应的能力。本研究评估了经口给予幼小牛的基因缺失 MAP 菌株,称为疫苗的功效。该研究旨在评估其控制 MAP 肠道感染的效果,并研究粘膜接种引起的免疫反应。该研究代表了在幼小牛口服 MAP 挑战的背景下对肠道改良活 MAP 疫苗的首次评估。口服免疫接种减少了 MAP 在回肠和回盲瓣中的定植。这种部分保护的免疫反应与接种动物中具有促炎表型(IFNγ+/TNFα+)的 CD4+和 CD8+T 细胞的频率增加有关。此外,从接种动物的再刺激 PBMC 显示出在挑战后 10-12 周时表达增加。此外,免疫表型分析血液白细胞表明,接种的小牛具有更高水平的表达细胞表面标志物的 T 细胞,这些标志物与长期中枢记忆一致。总体而言,我们的研究结果为针对牛 JD 的改良活 MAP 疫苗的开发和免疫原性提供了新的见解,证明口服疫苗可以刺激宿主免疫反应,从而对肠道 MAP 感染具有保护作用。
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