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肺树突状细胞通过趋化因子受体 CCR4 给 T 细胞打上肺归巢的“烙印”并促进肺部免疫。

Lung dendritic cells imprint T cell lung homing and promote lung immunity through the chemokine receptor CCR4.

机构信息

Center for Immunology and Inflammatory Diseases, Division of Rheumatology, Allergy, and Immunology, Massachusetts General Hospital, Harvard Medical School, Charlestown, MA 02129, USA.

出版信息

J Exp Med. 2013 Aug 26;210(9):1855-69. doi: 10.1084/jem.20130091. Epub 2013 Aug 19.

Abstract

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.

摘要

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。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e56f/3754856/d0486dfdec01/JEM_20130091_Fig1.jpg

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