Department of Immunology, University of Toronto, Toronto, ON, Canada.
Biological Sciences, Sunnybrook Research Institute, Toronto, ON, Canada.
Clin Exp Immunol. 2023 Jul 5;213(1):13-22. doi: 10.1093/cei/uxad048.
The Forkhead Box P3 (FOXP3) protein is an essential transcription factor for the development and function of regulatory T cells (Tregs), involved in the maintenance of immunological tolerance. Although extensive research over the last decade has investigated the critical role of FOXP3+ cells in preserving immune homeostasis, our understanding of their specific functions remains limited. Therefore, unveiling the molecular mechanisms underpinning the up- and downstream transcriptional regulation of and by FOXP3 is crucial for developing Treg-targeted therapeutics. Dysfunctions in FOXP3+ Tregs have also been found to be inherent drivers of autoimmune disorders and have been shown to exhibit multifaceted functions in the context of cancer. Recent research suggests that these cells may also be involved in tissue-specific repair and regeneration. Herein, we summarize current understanding of the thymic-transcriptional regulatory landscape of FOXP3+ Tregs, their epigenetic modulators, and associated signaling pathways. Finally, we highlight the contributions of FOXP3 on the functional development of Tregs and reflect on the clinical implications in the context of pathological and physiological immune responses.
叉头框蛋白 P3(FOXP3)蛋白是调节性 T 细胞(Treg)发育和功能所必需的转录因子,参与维持免疫耐受。尽管在过去十年中进行了广泛的研究,探讨了 FOXP3+细胞在维持免疫稳态中的关键作用,但我们对其特定功能的理解仍然有限。因此,揭示 FOXP3 及其上游和下游转录调控的分子机制对于开发针对 Treg 的治疗方法至关重要。FOXP3+Treg 的功能障碍也被发现是自身免疫疾病的固有驱动因素,并已被证明在癌症背景下具有多方面的功能。最近的研究表明,这些细胞也可能参与组织特异性修复和再生。本文总结了目前对 FOXP3+Treg 的胸腺转录调控景观、表观遗传调节剂及其相关信号通路的理解,最后强调了 FOXP3 对 Treg 功能发育的贡献,并结合病理和生理免疫反应探讨了其临床意义。