Centre International de Recherche en Infectiologie, INSERM, U1111, Université Claude Bernard Lyon 1, CNRS, UMR5308, École Normale Supérieure de Lyon, Université de Lyon, F-69007 Lyon, France; and.
Altrabio, F-69007 Lyon, France.
J Immunol. 2018 May 15;200(10):3635-3646. doi: 10.4049/jimmunol.1701698. Epub 2018 Apr 9.
The pool of memory-phenotype CD8 T cells is composed of Ag-induced (AI) and cytokine-induced innate (IN) cells. IN cells have been described as having properties similar to those of AI memory cells. However, we found that pathogen-induced AI memory cells can be distinguished in mice from naturally generated IN memory cells by surface expression of NKG2D. Using this marker, we described the increased functionalities of AI and IN memory CD8 T cells compared with naive cells, as shown by comprehensive analysis of cytokine secretion and gene expression. However, AI differed from IN memory CD8 T cells by their capacity to migrate to the lung parenchyma upon inflammation or infection, a process dependent on their expression of ITGA1/CD49a and ITGA4/CD49d integrins.
记忆表型 CD8 T 细胞库由抗原诱导(AI)和细胞因子诱导的固有(IN)细胞组成。IN 细胞被描述为具有类似于 AI 记忆细胞的特性。然而,我们发现,病原体诱导的 AI 记忆细胞可以通过表面表达 NKG2D 在小鼠中与天然产生的 IN 记忆细胞区分开来。使用这个标记物,我们通过对细胞因子分泌和基因表达的综合分析,描述了 AI 和 IN 记忆 CD8 T 细胞与幼稚细胞相比的增强功能。然而,AI 记忆 CD8 T 细胞与 IN 记忆 CD8 T 细胞的不同之处在于,它们在炎症或感染时向肺实质迁移的能力,这一过程依赖于它们表达 ITGA1/CD49a 和 ITGA4/CD49d 整合素。