Division of Immunology, Netherlands Cancer Institute, 1066 CX Amsterdam, Netherlands.
Division of Biological Stress Response, Netherlands Cancer Institute, 1066 CX Amsterdam, Netherlands.
Science. 2014 Oct 3;346(6205):101-5. doi: 10.1126/science.1254803. Epub 2014 Aug 28.
After an infection, pathogen-specific tissue-resident memory T cells (T(RM) cells) persist in nonlymphoid tissues to provide rapid control upon reinfection, and vaccination strategies that create T(RM) cell pools at sites of pathogen entry are therefore attractive. However, it is not well understood how T(RM) cells provide such pathogen protection. Here, we demonstrate that activated T(RM) cells in mouse skin profoundly alter the local tissue environment by inducing a number of broadly active antiviral and antibacterial genes. This "pathogen alert" allows skin T(RM) cells to protect against an antigenically unrelated virus. These data describe a mechanism by which tissue-resident memory CD8(+) T cells protect previously infected sites that is rapid, amplifies the activation of a small number of cells into an organ-wide response, and has the capacity to control escape variants.
感染后,病原体特异性组织驻留记忆 T 细胞(T(RM) 细胞)在非淋巴组织中持续存在,以便在再次感染时提供快速控制,因此,在病原体进入部位产生 T(RM) 细胞池的疫苗接种策略具有吸引力。然而,人们尚不清楚 T(RM) 细胞如何提供这种病原体保护。在这里,我们证明激活的 T(RM) 细胞在小鼠皮肤中通过诱导多种广泛有效的抗病毒和抗细菌基因来深刻改变局部组织环境。这种“病原体警报”使皮肤 T(RM) 细胞能够抵御抗原上无关的病毒。这些数据描述了组织驻留记忆 CD8(+) T 细胞保护先前感染部位的机制,该机制快速、将少数细胞的激活放大为器官范围的反应,并且具有控制逃逸变体的能力。