Harnessing the potential of γδ T cells through engineering and combination treatment for cancer therapies

γδT cells comprise 1-10% of circulating T cells, are further enriched in barrier tissues such as the gut and skin, and also form a critical component of lymphoid stress surveillance. γδ T cells have been gaining prominence as an alternative to αβ T cells for cancer immunotherapy. Such popularity may be attributed to multiple factors including the MHC-independent nature of γδ T activation, which differentiates them from αβ T cells and underlies their lack of alloreactivity. In this Review, we describe efforts to optimize the potential of γδ T cells as a cancer immunotherapeutic. We discuss the impact of disease burden on efficacy and the contexts in which unmodified γδ T cells have succeeded or failed to yield durable responses. Finally, we explore options for enhancing γδ T cell efficacy including combinations with other treatments and engineering strategies to capitalize on their potency. Adoptive cell transfer therapies using αβ T cells have made strides in medical translation, but the application of γδ T cells remains a work-in-progress. Here the authors summarize the unique biological properties, means of engineering, regime for treatment, and future research directions that may help realize γδ T cells’ potential for the clinics.

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Publication Details

Journal
Nature Communications
Published
2026-05-22
DOI
https://doi.org/10.1038/s41467-026-73451-z
Primary Topic
Immune Cell Function and Interaction
Type
article
Field-Weighted Citation Impact
0.00
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article

Harnessing the potential of γδ T cells through engineering and combination treatment for cancer therapies

Marta Barisa, Jonathan Fisher, Daniel Abate-Daga, Yin Wu et al.
Nature Communications
Immune Cell Function and Interaction
article

Harnessing the potential of γδ T cells through engineering and combination treatment for cancer therapies

Marta Barisa, Jonathan Fisher, Daniel Abate-Daga, Yin Wu, Lawrence Lamb
article en

Abstract

γδT cells comprise 1-10% of circulating T cells, are further enriched in barrier tissues such as the gut and skin, and also form a critical component of lymphoid stress surveillance. γδ T cells have been gaining prominence as an alternative to αβ T cells for cancer immunotherapy. Such popularity may be attributed to multiple factors including the MHC-independent nature of γδ T activation, which differentiates them from αβ T cells and underlies their lack of alloreactivity. In this Review, we describe efforts to optimize the potential of γδ T cells as a cancer immunotherapeutic. We discuss the impact of disease burden on efficacy and the contexts in which unmodified γδ T cells have succeeded or failed to yield durable responses. Finally, we explore options for enhancing γδ T cell efficacy including combinations with other treatments and engineering strategies to capitalize on their potency. Adoptive cell transfer therapies using αβ T cells have made strides in medical translation, but the application of γδ T cells remains a work-in-progress. Here the authors summarize the unique biological properties, means of engineering, regime for treatment, and future research directions that may help realize γδ T cells’ potential for the clinics.

Nature Communications
King's College London (GB), Great Ormond Street Hospital (GB), Moffitt Cancer Center (US), United Biomedical (United States) (US), CRUK Lung Cancer Centre of Excellence (GB), University College London (GB)
Openalex Percentile: Top 8%
Immune Cell Function and Interaction
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