Luo Annie, Leach Steven T, Barres Romain, Hesson Luke B, Grimm Michael C, Simar David
St George and Sutherland Clinical School, University of New South Wales, Sydney, NSW, Australia.
School of Women and Children's Health, University of New South Wales, Sydney, NSW, Australia.
Front Immunol. 2017 Apr 10;8:417. doi: 10.3389/fimmu.2017.00417. eCollection 2017.
Immune cells not only affect tissue homeostasis at the site of inflammation but also exert systemic effects contributing to multiple chronic conditions. Recent evidence clearly supports an altered T helper 17/regulatory T cell (Th17/Treg) balance leading to the development and progression of inflammatory diseases that not only affect the gastrointestinal tract but also have whole-body manifestations, including insulin resistance. Epigenetic mechanisms are amenable to both environmental and circulating factors and contribute to determining the T cell landscape. The recently identified participation of the gut microbiota in the remodeling of the epigenome of immune cells has triggered a paradigm shift in our understanding of the etiology of various inflammatory diseases and opened new paths toward therapeutic strategies. In this review, we provide an overview of the contribution of the Th17/Treg balance in the development and progression of inflammatory bowel diseases and metabolic diseases. We discuss the involvement of epigenetic mechanisms in the regulation of T cell function in the particular context of dysbiosis. Finally, we examine the potential for nutritional interventions affecting the gut microbiota to reshape the T cell epigenome and address the inflammatory component of various diseases.
免疫细胞不仅影响炎症部位的组织稳态,还会产生全身性影响,引发多种慢性疾病。最近的证据明确支持辅助性T细胞17/调节性T细胞(Th17/Treg)平衡的改变会导致炎症性疾病的发生和发展,这些疾病不仅影响胃肠道,还会出现包括胰岛素抵抗在内的全身表现。表观遗传机制受环境和循环因子的影响,并有助于确定T细胞格局。最近发现肠道微生物群参与免疫细胞表观基因组的重塑,这引发了我们对各种炎症性疾病病因理解的范式转变,并为治疗策略开辟了新途径。在这篇综述中,我们概述了Th17/Treg平衡在炎症性肠病和代谢性疾病发生发展中的作用。我们讨论了在生态失调的特定背景下,表观遗传机制在调节T细胞功能中的作用。最后,我们研究了影响肠道微生物群的营养干预措施重塑T细胞表观基因组并解决各种疾病炎症成分的潜力。