Center for Immunology and Inflammatory Diseases, Division of Rheumatology, Allergy, and Immunology, Massachusetts General Hospital, Harvard Medical School, Charlestown, MA 02129, USA.
J Exp Med. 2013 Aug 26;210(9):1855-69. doi: 10.1084/jem.20130091. Epub 2013 Aug 19.
T cell trafficking into the lung is critical for lung immunity, but the mechanisms that mediate T cell lung homing are not well understood. Here, we show that lung dendritic cells (DCs) imprint T cell lung homing, as lung DC-activated T cells traffic more efficiently into the lung in response to inhaled antigen and at homeostasis compared with T cells activated by DCs from other tissues. Consequently, lung DC-imprinted T cells protect against influenza more effectively than do gut and skin DC-imprinted T cells. Lung DCs imprint the expression of CCR4 on T cells, and CCR4 contributes to T cell lung imprinting. Lung DC-activated, CCR4-deficient T cells fail to traffic into the lung as efficiently and to protect against influenza as effectively as lung DC-activated, CCR4-sufficient T cells. Thus, lung DCs imprint T cell lung homing and promote lung immunity in part through CCR4.
T 细胞向肺部的迁移对于肺部免疫至关重要,但介导 T 细胞向肺部归巢的机制尚不清楚。在这里,我们表明,肺部树突状细胞 (DC) 可对 T 细胞向肺部的归巢进行“印记”,因为与由其他组织的 DC 激活的 T 细胞相比,肺部 DC 激活的 T 细胞在响应吸入的抗原和在体内平衡时更有效地向肺部迁移。因此,肺部 DC 印记的 T 细胞比肠道和皮肤 DC 印记的 T 细胞更有效地预防流感。肺部 DC 在 T 细胞上“印记”CCR4 的表达,而 CCR4 有助于 T 细胞向肺部的“印记”。与肺部 DC 激活的 CCR4 充足的 T 细胞相比,肺部 DC 激活的、CCR4 缺陷的 T 细胞不能有效地向肺部迁移,也不能像肺部 DC 激活的、CCR4 充足的 T 细胞那样有效地预防流感。因此,肺部 DC 通过 CCR4 对 T 细胞向肺部的归巢进行“印记”并促进肺部免疫。