Abstract
Human γδ T cells are a rare but functionally diverse lymphocyte subset critical for tumor surveillance and antimicrobial immunity. Although they express NK cell–associated receptors such as killer-cell immunoglobulin-like receptors (KIRs), the relevance of KIR expression on γδ T cells remains largely unexplored. Using flow cytometry, ATAC-seq, and RNA-seq, we identified KIR expression as a marker that distinguished 2 functionally and molecularly distinct γδ T cell subsets. KIR+ γδ T cells exhibited an advanced, memory-like differentiation state characterized by heightened cytotoxicity, stable epigenetic remodeling, and a predominant IFN-γ–producing profile. In contrast, KIR– γδ T cells maintained a naive-like phenotype and preferentially produced IL-17 upon polarization. Notably, KIR+ γδ T cells were consistently observed across individuals but were significantly enriched in cytomegalovirus (CMV)-seropositive donors, suggesting that chronic antigenic stimulation could promote the emergence of KIR+ effector γδ T cells. These findings reveal a functional dichotomy in human γδ T cells defined by KIR expression, linking IFN-γ–driven cytotoxicity with KIR+ cells and IL-17 production with KIR– cells. This insight advances our understanding of γδ T cell heterogeneity and has implications for viral immunity, immune memory, and the development of γδ T cell–based immunotherapies.
Authors
Mahya Razmi, Yeganeh Almasi, Marilee Larrivée, Jonathan B. Angel, Alexandre Blais, Zakia Djaoud
Figure 4
Epigenetic and transcriptomic profiling of γδ T cells reveals a KIR associated divergence.
