Department of Life Science, College of Natural Sciences, Hanyang University, Seoul, Republic of Korea.
Research Institute for Natural Sciences, Hanyang University, Seoul, Republic of Korea.
Exp Mol Med. 2017 Aug 4;49(8):e364. doi: 10.1038/emm.2017.102.
The prevalence of autoimmune, infectious and metabolic diseases is different for men and women owing to the respective ability of their immune systems to respond to self and foreign antigens. Although several factors, including hormones and the X-chromosome, have been suggested to contribute to such sex-specific immune responses, the underlying factors remain poorly defined. Recent studies using peroxisome proliferator-activated receptor (PPAR) ligands and knockout mice have identified sex-dimorphic expression of PPARs, and have shown that the inhibitory functions of PPAR in T cells are substantially affected by the sex hormones. In this review, we consider the sex-specific differences in PPARs and summarize the diverse PPAR-mediated, sex-specific properties of effector T-cell responses, such as T-cell activation, survival and differentiation, as well as their involvement in T-cell-related autoimmune diseases, including colitis, graft-versus-host disease and experimental autoimmune encephalomyelitis. Understanding PPAR-mediated sex differences in immune responses will provide more precise insights into the roles of PPARs in effector T cells.
由于免疫系统对自身和外来抗原的反应能力不同,男性和女性患自身免疫性、感染性和代谢性疾病的流行率也不同。尽管有几种因素,包括激素和 X 染色体,被认为有助于这种性别特异性免疫反应,但潜在的因素仍未得到很好的定义。最近使用过氧化物酶体增殖物激活受体 (PPAR) 配体和敲除小鼠的研究已经确定了 PPAR 的性别二态性表达,并表明 PPAR 在 T 细胞中的抑制功能受到性激素的显著影响。在这篇综述中,我们考虑了 PPAR 的性别特异性差异,并总结了 PPAR 介导的效应 T 细胞反应的多种性别特异性特性,如 T 细胞激活、存活和分化,以及它们在与 T 细胞相关的自身免疫性疾病中的作用,包括结肠炎、移植物抗宿主病和实验性自身免疫性脑脊髓炎。了解 PPAR 介导的免疫反应中的性别差异将为 PPAR 在效应 T 细胞中的作用提供更精确的见解。