Current companies developing γδ T cell-based immunotherapies
Company | γδ T cell type | Allogeneic vs. autologous | Targeting strategy/engineering |
---|---|---|---|
GammaCell Biotechnologies | Vδ2 | Autologous/allogeneic | Unmodified |
Hebei Senlang Biotechnology | Vδ2 | Autologous | CAR/αβTCR |
Incysus Therapeutics | Vδ2 | Autologous | Engineered for chemo-resistance |
Adicet Bio, Inc. | Vδ1 | Allogeneic | CAR |
Beijing Doing Biomedical | Vδ2 | Allogeneic | Unmodified/CAR |
Cytomed Therapeutics | Vδ2 | Allogeneic | CAR |
GammaDelta Therapeutics | Vδ1 | Allogeneic | CAR |
Immatics | Vδ2 | Allogeneic | αβTCR |
PhosphoGam Inc. | Vδ2 | Allogeneic | Unmodified |
TC BioPharm | Vδ1/Vδ2 | Autologous/allogeneic | Unmodified/CAR |
Imcheck Therapeutics | Vδ2 | Autologous (in vivo) | Vδ2 activation with BTN3A |
Lava Therapeutics | Vδ2 | Autologous (in vivo) | Activated Vδ2 with BiTE |
PersonGen BioTherapeutics | γδ T | Allogeneic | TAA3-UCAR, CD7 UCAR |
Expression Therapeutics | Vδ2 | Allogeneic | Unmodified/CAR |
UCAR: universal CAR
Note. Adapted from "Cancer immunotherapy with γδ T cells: many paths ahead of us", by Kabelitz D, Serrano R, Kouakanou L, Peters C, Kalyan S. Cell Mol Immunol. 2020;17:925–39 (https://www.nature.com/articles/s41423-020-0504-x). CC-BY.
NJ and SSR both wrote the first draft, edited, read and approved the submitted version.
The authors declare that they have no conflicts of interest.
Not applicable.
Not applicable.
Not applicable.
Not applicable.
This work was supported by the K08CA248962 grant (S.S.R.) from the National Cancer Institute (NCI) of the National Institutes of Health (NIH). The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.
© The Author(s) 2022.