Liang Dongchun, Shao Hui, Born Willi K, O'Brien Rebecca L, Kaplan Henry J, Sun Deming
Doheny Eye Institute and Department of Ophthalmology, David Geffen School of Medicine at UCLA, Los Angeles, California.
Department of Ophthalmology and Visual Sciences, Kentucky Lions Eye Center, University of Louisville, Louisville, Kentucky.
Crit Rev Immunol. 2018;38(3):233-243. doi: 10.1615/CritRevImmunol.2018026150.
Regulatory effects of γδ T-cells on immune responses have been studied for years. We have investigated the regulatory effect of γδ T-cells on Th1 and Th17 autoimmune responses, and have studied molecular and cellular mechanisms by which γδ T-cells enhance or inhibit immune responses, exploiting a well-characterized murine model of experimental autoimmune uveitis (EAU). Our results show that (1) aberrant γδ T-cell activation is an important pathogenic event in EAU; (2) γδ T-cells have a unique regulatory effect on Th17 autoimmune responses, which is shaped by the activation status of γδ T-cells; and (3) γδ-mediated immunoregulation is closely linked with the extracellular adenosine metabolism. Reciprocal interactions between γδ T-cells and extracellular adenosine partially determine the development of EAU.
多年来,γδ T细胞对免疫反应的调节作用一直是研究热点。我们研究了γδ T细胞对Th1和Th17自身免疫反应的调节作用,并利用特征明确的实验性自身免疫性葡萄膜炎(EAU)小鼠模型,研究了γδ T细胞增强或抑制免疫反应的分子和细胞机制。我们的研究结果表明:(1)γδ T细胞异常激活是EAU的一个重要致病事件;(2)γδ T细胞对Th17自身免疫反应具有独特的调节作用,这种作用由γδ T细胞的激活状态决定;(3)γδ介导的免疫调节与细胞外腺苷代谢密切相关。γδ T细胞与细胞外腺苷之间的相互作用部分决定了EAU的发展。