ResearchIn-Press PreviewAIDS/HIVImmunology
Open Access |
10.1172/jci.insight.198185
1Department of Microbiology, Immunology and Tropical Medicine, The George Washington University, Washington, DC, United States of America
2Department of Medicine, The George Washington University, Washington, DC, United States of America
3Department of Microbiology, Immunology and Tropical Medicine, Department of, The George Washingtom University, Washington, DC, United States of America
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1Department of Microbiology, Immunology and Tropical Medicine, The George Washington University, Washington, DC, United States of America
2Department of Medicine, The George Washington University, Washington, DC, United States of America
3Department of Microbiology, Immunology and Tropical Medicine, Department of, The George Washingtom University, Washington, DC, United States of America
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1Department of Microbiology, Immunology and Tropical Medicine, The George Washington University, Washington, DC, United States of America
2Department of Medicine, The George Washington University, Washington, DC, United States of America
3Department of Microbiology, Immunology and Tropical Medicine, Department of, The George Washingtom University, Washington, DC, United States of America
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1Department of Microbiology, Immunology and Tropical Medicine, The George Washington University, Washington, DC, United States of America
2Department of Medicine, The George Washington University, Washington, DC, United States of America
3Department of Microbiology, Immunology and Tropical Medicine, Department of, The George Washingtom University, Washington, DC, United States of America
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1Department of Microbiology, Immunology and Tropical Medicine, The George Washington University, Washington, DC, United States of America
2Department of Medicine, The George Washington University, Washington, DC, United States of America
3Department of Microbiology, Immunology and Tropical Medicine, Department of, The George Washingtom University, Washington, DC, United States of America
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1Department of Microbiology, Immunology and Tropical Medicine, The George Washington University, Washington, DC, United States of America
2Department of Medicine, The George Washington University, Washington, DC, United States of America
3Department of Microbiology, Immunology and Tropical Medicine, Department of, The George Washingtom University, Washington, DC, United States of America
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Published February 10, 2026 - More info
Latently infected cells persist in people living with HIV (PWH) despite suppressive antiretroviral therapy (ART) and evade immune clearance. Shock and Kill cure strategies are hampered by insufficient enhancement of targeted immune responses following latency reversal. We previously demonstrated autologous Vδ2 T cells from PWH retain anti-HIV activity and can reduce CD4+ T cell reservoirs, although their use in cure approaches is limited due to their dual role as a viral reservoir. However, promising clinical data in oncology shows their unique MHC- unrestricted antigen recognition affords potent on-target cytotoxicity in the absence of graft-versus-host disease when used as an allogeneic adoptive cell therapy modality. Here, we found expanded allogeneic Vδ2 T cells specifically eliminated HIV-infected CD4+ T cells and monocyte-derived macrophages (MDM), overcoming inherent resistance to killing by other cell types such as NK and CD8+ T cells. Notably, we demonstrated allogeneic Vδ2 T cells recognized and eliminated the HIV-latent CD4+ T cell reservoir following latency reversal. Our study provides evidence for developing an allogeneic γδ T cell therapy for HIV cure and warrants pre-clinical investigation in combination approaches.