Department of Veterinary Microbiology and Preventative Medicine, Iowa State University, Ames, Iowa, United States of America.
Interdepartmental Microbiology Program, Iowa State University, Ames, Iowa, United States of America.
PLoS One. 2019 Feb 22;14(2):e0212751. doi: 10.1371/journal.pone.0212751. eCollection 2019.
Mycobacterium bovis Bacillus Calmette-Guérin (BCG) is a live attenuated vaccine for use against tuberculosis (TB); however, it is known to reduce childhood mortality from infections other than TB. The unspecific protection induced by BCG vaccination has been associated with the induction of memory-like traits of the innate immune system identified as 'trained' immunity. In humans and mouse models, in vitro and in vivo BCG training leads to enhanced production of monocyte-derived proinflammatory cytokines in response to secondary unrelated bacterial and fungal pathogens. While BCG has been studied extensively for its ability to induce innate training in humans and mouse models, BCG's nonspecific protective effects have not been defined in agricultural species. Here, we show that in vitro BCG training induces a functional change in bovine monocytes, characterized by increased transcription of proinflammatory cytokines upon restimulation with the toll-like receptor agonists. Importantly, in vivo, aerosol BCG vaccination in young calves also induced a 'trained' phenotype in circulating peripheral blood mononuclear cells (PBMCs), that lead to a significantly enhanced TLR-induced proinflammatory cytokine response and changes in cellular metabolism compared to PBMCs from unvaccinated control calves. Similar to the long-term training effects of BCG reported in humans, our results suggest that in young calves, the effects of BCG induced innate training can last for at least 3 months in circulating immune populations. Interestingly, however, aerosol BCG vaccination did not 'train' the innate immune response at the mucosal level, as alveolar macrophages from aerosol BCG vaccinated calves did not mount an enhanced inflammatory response to secondary stimulation, compared to cells isolated from control calves. Together, our results suggest that, like mice and humans, the innate immune system of calves can be 'trained'; and that BCG vaccination could be used as an immunomodulatory strategy to reduce disease burden in juvenile food animals before the adaptive immune system has fully matured.
牛分枝杆菌卡介苗(BCG)是一种用于预防结核病(TB)的减毒活疫苗;然而,它已知可降低除结核病以外的其他感染导致的儿童死亡率。BCG 疫苗接种诱导的非特异性保护与先天免疫系统记忆样特征的诱导有关,这些特征被认为是“训练”的免疫。在人类和小鼠模型中,体外和体内 BCG 训练导致单核细胞衍生的促炎细胞因子的产生增加,以响应二次非相关细菌和真菌病原体。虽然已经在人类和小鼠模型中广泛研究了 BCG 诱导先天训练的能力,但 BCG 在农业物种中的非特异性保护作用尚未确定。在这里,我们表明,体外 BCG 训练诱导牛单核细胞的功能变化,其特征是在重新刺激 Toll 样受体激动剂时促炎细胞因子的转录增加。重要的是,在体内,年轻牛犊的气溶胶 BCG 疫苗接种也在循环外周血单核细胞(PBMC)中诱导出“训练”表型,与未接种疫苗的对照牛犊的 PBMC 相比,这导致 TLR 诱导的促炎细胞因子反应和细胞代谢的显著增强。与在人类中报道的 BCG 的长期训练效应相似,我们的结果表明,在年轻牛犊中,BCG 诱导的先天训练的作用至少可以在循环免疫群体中持续 3 个月。然而,有趣的是,气溶胶 BCG 疫苗接种并没有在黏膜水平上“训练”先天免疫反应,因为与来自对照牛犊的细胞相比,来自气溶胶 BCG 接种牛犊的肺泡巨噬细胞对二次刺激不会产生增强的炎症反应。总之,我们的结果表明,与小鼠和人类一样,牛犊的先天免疫系统可以“训练”;并且 BCG 疫苗接种可以作为一种免疫调节策略,在适应性免疫系统尚未完全成熟之前,减少幼年食用动物的疾病负担。