Institute of Microbiology, ETH Zürich, 8093 Zürich, Switzerland.
Institute of Microbiology, ETH Zürich, 8093 Zürich, Switzerland.
Cell Rep. 2015 Nov 10;13(6):1125-1136. doi: 10.1016/j.celrep.2015.09.082. Epub 2015 Oct 29.
Tissue-resident memory T cells (TRM) reside in barrier tissues and provide local immediate protective immunity. Here, we show that the salivary gland (SG) most-effectively induces CD8(+) and CD4(+) TRM cells against murine cytomegalovirus (MCMV), which persists in and spreads from this organ. TRM generation depended on local antigen for CD4(+), but not CD8(+), TRM cells, highlighting major differences in T cell subset-specific demands for TRM development. CMV-specific CD8(+) T cells fail to control virus replication upon primary infection in the SG due to CMV-induced MHC I downregulation in glandular epithelial cells. Using intraglandular infection, we challenge this notion and demonstrate that memory CD8(+) T cells confer immediate protection against locally introduced MCMV despite active viral immune evasion, owing to early viral tropism to cells that largely withstand MHC I downregulation. Thus, we unravel a yet-unappreciated role for memory CD8(+) T cells in protecting mucosal tissues against CMV infection.
组织驻留记忆 T 细胞(TRM)存在于屏障组织中,提供局部即刻保护免疫。在这里,我们表明唾液腺(SG)最有效地诱导针对小鼠巨细胞病毒(MCMV)的 CD8(+)和 CD4(+)TRM 细胞,该病毒存在于并从该器官传播。TRM 的产生取决于局部抗原,用于 CD4(+),但不是 CD8(+),TRM 细胞,突出了 T 细胞亚群特异性对 TRM 发育的需求的主要差异。由于 CMV 诱导的 SG 上皮细胞中 MHC I 下调,CMV 特异性 CD8(+)T 细胞在 SG 中的初次感染中无法控制病毒复制。通过腺内感染,我们挑战了这一观点,并证明记忆 CD8(+)T 细胞尽管存在病毒免疫逃逸,但仍能立即提供针对局部引入的 MCMV 的保护,这是由于早期病毒对细胞的嗜性,这些细胞在很大程度上抵抗 MHC I 下调。因此,我们揭示了记忆 CD8(+)T 细胞在保护粘膜组织免受 CMV 感染方面的尚未被充分认识的作用。