Sato Wakiro, Aranami Toshimasa, Yamamura Takashi
Department of Immunology, National Institute of Neuroscience, National Center of Neurology and Psychiatry, 4-1-1 Ogawahigashi, Kodaira, Tokyo 187-8502, Japan.
J Immunol. 2007 Jun 15;178(12):7525-9. doi: 10.4049/jimmunol.178.12.7525.
Recent reports have shown that IL-17-producing CD4+ T cells (Th17 cells) belong to a distinct helper T cell lineage and are critically involved in the pathogenesis of autoimmune diseases and allergies. However, the chemokine receptor profile of Th17 cells remains to be clarified. In this study, we report that human Th17 cells are identified as CCR2+CCR5- memory CD4+ T cells. Analysis of PBMC from healthy donors showed that CCR2+ cells produce much larger amounts of IL-17 than CCR2- cells, indicating the preferential expression of CCR2 on Th17 cells. Notably, CCR2+CCR5- memory CD4+ T cells produced a large amount of IL-17 and little IFN-gamma, whereas CCR2+CCR5+ cells reciprocally produced an enormous amount of IFN-gamma but little IL-17. Moreover, a higher expression of T-bet was seen in the CCR5+ memory T cells. These results indicate that absence of CCR5 distinguishes human Th17 cells from Th1 cells.
最近的报告显示,产生白细胞介素-17的CD4+ T细胞(Th17细胞)属于一种独特的辅助性T细胞谱系,并且在自身免疫性疾病和过敏症的发病机制中起关键作用。然而,Th17细胞的趋化因子受体谱仍有待阐明。在本研究中,我们报告人类Th17细胞被鉴定为CCR2+CCR5-记忆性CD4+ T细胞。对健康供体的外周血单个核细胞分析显示,CCR2+细胞比CCR2-细胞产生的白细胞介素-17量要多得多,这表明CCR2在Th17细胞上优先表达。值得注意的是,CCR2+CCR5-记忆性CD4+ T细胞产生大量白细胞介素-17且很少产生干扰素-γ,而CCR2+CCR5+细胞则相反,产生大量干扰素-γ但很少产生白细胞介素-17。此外,在CCR5+记忆性T细胞中观察到T-bet的表达更高。这些结果表明,CCR5的缺失将人类Th17细胞与Th1细胞区分开来。