ReviewFrontiers in immunology2026
Vγ9Vδ2 T cells in tuberculosis: protective immunity and translational perspectives.
Review in Frontiers in immunology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.
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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
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8 authors.
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Abstract
Background: Vγ9Vδ2 T cells constitute the predominant human circulating γδ T cell subset and serve as key mediators of anti-mycobacterial immunity through major histocompatibility complex (MHC)-unrestricted phosphoantigen recognition and rapid effector activation. Summary: This review evaluates Vγ9Vδ2 T cell biology in the context of tuberculosis (TB). We delineate the three-stage developmental pathway of Vγ9Vδ2 T cells in the postnatal thymus and the butyrophilin 3A1/2A1 (BTN3A1/BTN2A1)-mediated "inside-out" antigen sensing mechanism, noting the limitations of extrapolating Conclusion: Vγ9Vδ2 T cells offer distinct advantages for TB immunotherapy and vaccine design, but significant translational barriers remain. Future studies must address subset heterogeneity across infection stages, the epigenetic and metabolic reprogramming governing functional fate decisions, standardized correlates of protection, and BTN-targeted strategies validated in TB-specific preclinical models. The integration of single-cell multi-omics and CRISPR-based functional screening with γδ T cell biology offers a promising path toward clinical translation.
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