Center for Data Sciences, Brigham and Women's Hospital, Harvard Medical School, Boston, MA, USA.
Division of Genetics, Department of Medicine, Brigham and Women's Hospital and Harvard Medical School, Boston, MA, USA.
Nat Commun. 2024 Feb 8;15(1):1204. doi: 10.1038/s41467-024-45170-w.
Autoimmune disease heritability is enriched in T cell-specific regulatory regions of the genome. Modern-day T cell datasets now enable association studies between single nucleotide polymorphisms (SNPs) and a myriad of molecular phenotypes, including chromatin accessibility, gene expression, transcriptional programs, T cell antigen receptor (TCR) amino acid usage, and cell state abundances. Such studies have identified hundreds of quantitative trait loci (QTLs) in T cells that colocalize with genetic risk for autoimmune disease. The key challenge facing immunologists today lies in synthesizing these results toward a unified understanding of the autoimmune T cell: which genes, cell states, and antigens drive tissue destruction?
自身免疫性疾病的遗传率在基因组的 T 细胞特异性调节区域中得到了富集。现代 T 细胞数据集现在能够在单核苷酸多态性 (SNP) 与众多分子表型之间进行关联研究,包括染色质可及性、基因表达、转录程序、T 细胞抗原受体 (TCR) 氨基酸使用和细胞状态丰度。这些研究已经在 T 细胞中鉴定了数百个与自身免疫性疾病遗传风险相关的数量性状基因座 (QTL)。当今免疫学家面临的关键挑战在于综合这些结果,以对自身免疫性 T 细胞有一个统一的理解:哪些基因、细胞状态和抗原导致组织破坏?