Department of Microbiology and Immunology, Cornell University, Ithaca, NY 14853.
Department of Molecular Biology and Genetics, Cornell University, Ithaca, NY 14853.
Proc Natl Acad Sci U S A. 2022 Dec 6;119(49):e2212548119. doi: 10.1073/pnas.2212548119. Epub 2022 Nov 28.
Microbial exposure during development can elicit long-lasting effects on the health of an individual. However, how microbial exposure in early life leads to permanent changes in the immune system is unknown. Here, we show that the microbial environment alters the set point for immune susceptibility by altering the developmental architecture of the CD8+ T cell compartment. In particular, early microbial exposure results in the preferential expansion of highly responsive fetal-derived CD8+ T cells that persist into adulthood and provide the host with enhanced immune protection against intracellular pathogens. Interestingly, microbial education of fetal-derived CD8+ T cells occurs during thymic development rather than in the periphery and involves the acquisition of a more effector-like epigenetic program. Collectively, our results provide a conceptual framework for understanding how microbial colonization in early life leads to lifelong changes in the immune system.
在发育过程中接触微生物会对个体健康产生持久影响。然而,早期生活中的微生物暴露如何导致免疫系统发生永久性变化尚不清楚。在这里,我们表明微生物环境通过改变 CD8+T 细胞区室的发育结构来改变免疫易感性的设定点。具体而言,早期的微生物暴露导致高反应性胎儿衍生的 CD8+T 细胞的优先扩增,这些细胞持续存在于成年期,并为宿主提供针对细胞内病原体的增强免疫保护。有趣的是,胎儿衍生的 CD8+T 细胞的微生物教育发生在胸腺发育过程中,而不是在外周组织中,并且涉及获得更具效应器样的表观遗传程序。总的来说,我们的结果为理解早期生活中的微生物定植如何导致免疫系统终生变化提供了一个概念框架。