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.
Authors
- Marta Barisa (ORCID: https://orcid.org/0000-0001-7846-6810)
- Jonathan Fisher (ORCID: https://orcid.org/0000-0003-3302-2241)
- Daniel Abate-Daga (ORCID: https://orcid.org/0000-0002-2571-0215)
- Yin Wu (ORCID: https://orcid.org/0000-0003-4080-3935)
- Lawrence Lamb
Institutions
- 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)
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