{"title":"CD8+HLA-DR+CD27+ T cells define a population of naturally occurring regulatory precursors in humans","authors":"Huidong Guo, Bixia Wang, Zhigui Wu, Qi Zhang, Xinya Jiang, Fangqing Zhang, Jingrui Zhou, Shuang Fan, Yang Zhou, Zheng-Li Xu, Yu Wang, Xiang-Yu Zhao, Xiao-Jun Huang","doi":"10.1126/sciadv.adw1702","DOIUrl":null,"url":null,"abstract":"<div >Regulatory T<sub>reg</sub> cells are essential for immune homeostasis. While CD4 T<sub>reg</sub> cells are well characterized, CD8 T<sub>reg</sub> cells remain less understood and are primarily observed in pathological or experimental contexts. Here, we identify a naturally occurring CD8 regulatory precursor T<sub>rp</sub> cell at the steady state, defined by a CD8<sup>+</sup>HLA-DR<sup>+</sup>CD27<sup>+</sup> phenotype and a transcriptome resembling CD4 T<sub>reg</sub> cells. Multiomics analyses reveal activation of <i>TCF7</i> and costimulatory and co-inhibitory molecules in CD8 T<sub>rp</sub> cells. CD8 T<sub>rp</sub> cells suppress T cell expansion in vitro and in vivo. In a humanized xenogeneic graft-versus-host disease (GVHD) model, they dampen T cell activation, alleviate GVHD pathology, and prolong survival without impairing antileukemia activity. Mechanistically, CD8 T<sub>rp</sub> cells promote immune regulation by inducing FOXP3 expression in both CD4 T<sub>reg</sub> cells and themselves. Their expansion also correlates with immune homeostasis restoration post–allogeneic stem cell transplantation. These findings establish CD8 T<sub>rp</sub> cells as a naturally occurring regulatory precursor population that promotes transplantation tolerance.</div>","PeriodicalId":21609,"journal":{"name":"Science Advances","volume":"11 37","pages":""},"PeriodicalIF":12.5000,"publicationDate":"2025-09-10","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.science.org/doi/reader/10.1126/sciadv.adw1702","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Science Advances","FirstCategoryId":"103","ListUrlMain":"https://www.science.org/doi/10.1126/sciadv.adw1702","RegionNum":1,"RegionCategory":"综合性期刊","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"MULTIDISCIPLINARY SCIENCES","Score":null,"Total":0}
引用次数: 0
Abstract
Regulatory Treg cells are essential for immune homeostasis. While CD4 Treg cells are well characterized, CD8 Treg cells remain less understood and are primarily observed in pathological or experimental contexts. Here, we identify a naturally occurring CD8 regulatory precursor Trp cell at the steady state, defined by a CD8+HLA-DR+CD27+ phenotype and a transcriptome resembling CD4 Treg cells. Multiomics analyses reveal activation of TCF7 and costimulatory and co-inhibitory molecules in CD8 Trp cells. CD8 Trp cells suppress T cell expansion in vitro and in vivo. In a humanized xenogeneic graft-versus-host disease (GVHD) model, they dampen T cell activation, alleviate GVHD pathology, and prolong survival without impairing antileukemia activity. Mechanistically, CD8 Trp cells promote immune regulation by inducing FOXP3 expression in both CD4 Treg cells and themselves. Their expansion also correlates with immune homeostasis restoration post–allogeneic stem cell transplantation. These findings establish CD8 Trp cells as a naturally occurring regulatory precursor population that promotes transplantation tolerance.
期刊介绍:
Science Advances, an open-access journal by AAAS, publishes impactful research in diverse scientific areas. It aims for fair, fast, and expert peer review, providing freely accessible research to readers. Led by distinguished scientists, the journal supports AAAS's mission by extending Science magazine's capacity to identify and promote significant advances. Evolving digital publishing technologies play a crucial role in advancing AAAS's global mission for science communication and benefitting humankind.