4.7 Article

Allogeneic Vγ9Vδ2 T-cell immunotherapy exhibits promising clinical safety and prolongs the survival of patients with late-stage lung or liver cancer

期刊

CELLULAR & MOLECULAR IMMUNOLOGY
卷 18, 期 2, 页码 427-439

出版社

CHIN SOCIETY IMMUNOLOGY
DOI: 10.1038/s41423-020-0515-7

关键词

Allogeneic gamma delta T cells; New expansion formula; Cell therapy; Liver cancer; Lung cancer; Humanized mice

资金

  1. Key Program of the National Natural Science Foundation of China [31830021]
  2. Major International Joint Research Program of China [31420103901]
  3. 111 project [B16021]
  4. Scientific and Technological Plan of Guangdong Province [201704KW010]
  5. Fundamental Research Funds for the Central Universities, Natural Science Foundation of Guangdong Province, China [2020A1515010132]
  6. General Research Fund, Research Grants Council of Hong Kong [17122519, 17121214, 17115015, 17126317]
  7. Hong Kong SAR, China
  8. National Natural Science Foundation of China [31570898]
  9. Natural Science Foundation of Guangdong Province, China [2016A030313112]
  10. German Research Council (Deutsche Forschungsgemeinschaft) [Ka 502/19-1]
  11. Cluster of Excellence Inflammation-at-Interfaces (Deutsche Forschungsgemeinschaft) [ExC 306]
  12. China Postdoctoral Science Foundation [2017M622898]
  13. Postdoctoral Fund of the First Affiliated Hospital of Jinan University [809008]
  14. German Academic Exchange Service (DAAD)
  15. Erich und Gertrud Roggenbruck Foundation

向作者/读者索取更多资源

The study focused on utilizing allogeneic V gamma 9V delta 2 T cells for tumor immunotherapy, developing a novel formula for expanding gamma delta T cells from healthy donors, and conducting clinical trials to prove the safety and efficacy of allogeneic V gamma 9V delta 2 T cells, showing promising results in late-stage cancer patients.
V gamma 9V delta 2 T cells are promising candidates for cellular tumor immunotherapy. Due to their HLA-independent mode of action, allogeneic V gamma 9V delta 2 T cells can be considered for clinical application. To apply allogeneic V gamma 9V delta 2 T cells in adoptive immunotherapy, the methodology used to obtain adequate cell numbers with optimal effector function in vitro needs to be optimized, and clinical safety and efficacy also need to be proven. Therefore, we developed a novel formula to improve the expansion of peripheral gamma delta T cells from healthy donors. Then, we used a humanized mouse model to validate the therapeutic efficacy of expanded gamma delta T cells in vivo; furthermore, the expanded gamma delta T cells were adoptively transferred into late-stage liver and lung cancer patients. We found that the expanded cells possessed significantly improved immune effector functions, including proliferation, differentiation, and cancer cell killing, both in vitro and in the humanized mouse model. Furthermore, a phase I clinical trial in 132 late-stage cancer patients with a total of 414 cell infusions unequivocally validated the clinical safety of allogeneic V gamma 9V delta 2 T cells. Among these 132 patients, 8 liver cancer patients and 10 lung cancer patients who received >= 5 cell infusions showed greatly prolonged survival, which preliminarily verified the efficacy of allogeneic V gamma 9V delta 2 T-cell therapy. Our clinical studies underscore the safety and efficacy of allogeneic V gamma 9V delta 2 T-cell immunotherapy, which will inspire further clinical investigations and eventually benefit cancer patients.

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