Department of Microbiology, University of Georgia, Athens, GA 30602.
Center for Tropical and Emerging Global Diseases, University of Georgia, Athens, GA 30602; and.
J Immunol. 2020 Aug 1;205(3):573-578. doi: 10.4049/jimmunol.2000218. Epub 2020 Jun 26.
Myocytes express low levels of MHC class I (MHC I), perhaps influencing the ability of CD8 T cells to efficiently detect and destroy pathogens that invade muscle. infects many cell types but preferentially persists in muscle, and we asked if this tissue-dependent persistence was linked to MHC expression. Inducible enhancement of skeletal muscle MHC I in mice during the first 20 d of infection resulted in enhanced CD8-dependent reduction of parasite load. However, continued overexpression of MHC I beyond 30 d ultimately led to a collapse of systemic parasite control associated with immune exhaustion, which was reversible in part by blocking PD-1:PD-L1 interactions. These studies demonstrate a surprisingly strong and systemically dominant effect of skeletal muscle MHC expression on maintaining T cell function and pathogen control and argue that the normally low MHC I expression in skeletal muscle is host protective by allowing for pathogen control while preventing immune exhaustion.
肌细胞表达低水平的 MHC Ⅰ类分子(MHC I),这可能影响 CD8 T 细胞有效检测和破坏入侵肌肉的病原体的能力。寄生虫感染许多细胞类型,但优先在肌肉中持续存在,我们想知道这种组织依赖性的持续存在是否与 MHC 表达有关。在寄生虫感染的前 20 天,诱导小鼠骨骼肌 MHC I 的增强导致 CD8 依赖性寄生虫负荷的减少增强。然而,MHC I 的持续过度表达超过 30 天最终导致与免疫衰竭相关的系统性寄生虫控制崩溃,部分通过阻断 PD-1:PD-L1 相互作用而部分逆转。这些研究表明,骨骼肌 MHC 表达对维持 T 细胞功能和病原体控制具有惊人的强大和系统优势,并表明骨骼肌中通常较低的 MHC I 表达通过允许控制病原体而防止免疫衰竭,从而对宿主具有保护作用。