Division of Developmental Immunology, La Jolla Institute for Immunology, La Jolla, CA 92037.
Division of Vaccine Discovery, La Jolla Institute for Immunology, La Jolla, CA 92037.
Proc Natl Acad Sci U S A. 2022 Mar 8;119(10):e2113329119. doi: 10.1073/pnas.2113329119. Epub 2022 Mar 3.
SignificanceThe CD4 T response following acute infection is heterogeneous and deploys two distinct modes of suppression coinciding with initial pathogen exposure and resolution of infection. This bimodal suppression of CD8 T cells during priming and contraction is mediated by separate T lineages. These findings make a significant contribution to our understanding of the functional plasticity inherent within T, which allows these cells to serve as a sensitive and dynamic cellular rheostat for the immune system to prevent autoimmune pathology in the face of inflammation attendant to acute infection, enable expansion of the pathogen-specific response needed to control the infection, and reestablish immune homeostasis after the threat has been contained.
急性感染后 CD4 T 反应具有异质性,并采用两种不同的抑制模式,与初始病原体暴露和感染消退同时发生。这种在启动和收缩过程中对 CD8 T 细胞的双峰抑制是由不同的 T 细胞谱系介导的。这些发现为我们理解 T 细胞内在的功能可塑性做出了重要贡献,这使得这些细胞能够作为免疫系统的敏感和动态细胞变阻器,在急性感染伴随的炎症面前防止自身免疫病理学,使病原体特异性反应得以扩张以控制感染,并在威胁得到控制后重新建立免疫稳态。