Vaccines (Mar 2022)

Genetic Modification of T Cells for the Immunotherapy of Cancer

  • Suzanne Quinn,
  • Natasha Lenart,
  • Victoria Dronzek,
  • Gina M. Scurti,
  • Nasheed M. Hossain,
  • Michael I. Nishimura

DOI
https://doi.org/10.3390/vaccines10030457
Journal volume & issue
Vol. 10, no. 3
p. 457

Abstract

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Immunotherapy is a beneficial treatment approach for multiple cancers, however, current therapies are effective only in a small subset of patients. Adoptive cell transfer (ACT) is a facet of immunotherapy where T cells targeting the tumor cells are transferred to the patient with several primary forms, utilizing unmodified or modified T cells: tumor-infiltrating lymphocytes (TIL), genetically modified T cell receptor transduced T cells, and chimeric antigen receptor (CAR) transduced T cells. Many clinical trials are underway investigating the efficacy and safety of these different subsets of ACT, as well as trials that combine one of these subsets with another type of immunotherapy. The main challenges existing with ACT are improving clinical responses and decreasing adverse events. Current research focuses on identifying novel tumor targeting T cell receptors, improving safety and efficacy, and investigating ACT in combination with other immunotherapies.

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