Lewis-Sigler Institute for Integrative Genomics, Princeton University, Princeton, NJ.
Quantitative and Computational Biology Graduate Program, Princeton University, Princeton, NJ.
J Immunol. 2023 Apr 1;210(7):880-887. doi: 10.4049/jimmunol.2200864.
Regulatory T (Treg) cells are critical for tolerance to self-antigens and for preventing autoimmunity. Foxp3 has been identified as a Treg cell lineage-defining transcription factor controlling Treg cell differentiation and function. In this article, we review the current mechanistic and systemic understanding of Foxp3 function enabled by experimental and computational advances in high-throughput genomics.
调节性 T(Treg)细胞对于耐受自身抗原和预防自身免疫至关重要。Foxp3 已被确定为一种 Treg 细胞谱系定义转录因子,控制 Treg 细胞分化和功能。在本文中,我们通过高通量基因组学的实验和计算进展,综述了对 Foxp3 功能的当前机制和系统理解。