Mucida Daniel, Salek-Ardakani Shahram
Division of Developmental Immunology, La Jolla Institute for Allergy and Immunology, La Jolla, Calif 92037, USA.
J Allergy Clin Immunol. 2009 May;123(5):997-1003. doi: 10.1016/j.jaci.2009.03.016. Epub 2009 Apr 11.
The mucosal surfaces represent the main intersection between jawed vertebrates and the environment. The mucosal surface of the intestine alone forms the largest surface that is exposed to exogenous antigens as well as the largest collection of lymphoid tissue in the body. Therefore, a protective immune activity must coexist with efficient regulatory mechanisms to maintain a health status of these organisms. The discovery of a new lineage of T(H) cells that produce IL-17 has provided valuable new insight into host defense and the pathogenesis of inflammatory diseases at the mucosal surfaces. Of particular interest for these surfaces, it has been reported that peripherally-induced regulatory T cells and T(H)17 effector cells arise in a mutually exclusive fashion, depending on whether they are activated in the presence of TGF-beta or TGF-beta plus inflammatory cytokines such as IL-6. This review addresses the protective and pathogenic roles of T(H)17 cells in the mucosal surfaces and potential regulatory mechanisms that control their development.
粘膜表面是有颌脊椎动物与外界环境的主要交汇点。仅肠道的粘膜表面就构成了暴露于外源性抗原的最大表面积,同时也是体内最大的淋巴组织集合。因此,保护性免疫活动必须与有效的调节机制共存,以维持这些生物体的健康状态。产生白细胞介素-17的新型辅助性T细胞系的发现,为宿主防御以及粘膜表面炎症性疾病的发病机制提供了宝贵的新见解。对于这些表面而言,特别值得关注的是,据报道外周诱导的调节性T细胞和辅助性T17效应细胞以相互排斥的方式产生,这取决于它们是否在转化生长因子-β(TGF-β)或TGF-β加炎性细胞因子(如白细胞介素-6)存在的情况下被激活。本综述阐述了辅助性T17细胞在粘膜表面的保护和致病作用,以及控制其发育的潜在调节机制。