Epidermal γδ T cells, CD8 T cells and macrophages are increased in number in alopecia areata and express BST2 as part of an interferon-driven antiviral gene signature

Alopecia areata is an autoimmune disorder affecting approximately 2% of the global population, characterized by immune-mediated disruption of hair follicle immune privilege and unpredictable hair loss. While CD4 and CD8 T cells are established drivers of pathogenesis, the roles of other immune cell populations remain incompletely defined. Here, we reaffirm the pathogenic role of CD8 T cells and identify a contribution of epidermal γδ T cells and macrophages to alopecia areata. Using publicly available single-cell RNA sequencing (scRNAseq) data from the skin of C3H/HeJ mice with alopecia areata, we demonstrate that epidermal γδ T cells upregulate genes associated with immune homeostasis, proliferation, and inflammation, including BST2 , an interferon-stimulated antiviral protein. In vivo, epidermal γδ T cells and keratinocytes are increased in number, with BST2 expression enriched around hair follicles. BST2 is also expressed on CD8 T cells actively producing IFN-γ and on CD11b ⁺ macrophages with signatures of antiviral and complement system pathways. In human alopecia areata skin, BST2 expression is elevated in alopecia areata and downregulated following treatment with the JAK inhibitor tofacitinib. Together, these findings position BST2 as a marker of interferon-driven immune activation and highlight epidermal γδ T cells as a contributor to alopecia areata pathogenesis.