CD8<sup>+</sup>HLA-DR<sup>+</sup>CD27<sup>+</sup> T cells define a population of naturally occurring regulatory precursors in humans.

Guo, Huidong; Wang, Bixia; Wu, Zhigui; Zhang, Qi; Jiang, Xinya; Zhang, Fangqing; Zhou, Jingrui; Fan, Shuang et al. · Sci Adv · 2025

basic_science · Level V

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Abstract

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.

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