[T cell-based immunotherapies in solid tumors]

Bull Cancer. 2021 Oct;108(10S):S96-S108. doi: 10.1016/j.bulcan.2021.06.004.
[Article in French]

Abstract

In solid tumors, adoptive T cell therapies based on ex vivo amplification of antitumor T cell are represented by three main complementary approaches : (i) tumor infiltrating lymphocytes (TILs) which are amplified in vitro before reinjection to the patient, (ii) chimeric antigen receptor (CAR) engineered T cells and (iii) T cell receptor (TCR) engineered T cells. Despite encouraging results, some obstacles remain, such as optimal target selection and tumor microenvironment. In this Review, we discuss pros and cons of these different therapeutic strategies that may open new perspectives in the treatment of solid tumors.

Keywords: CAR T; CAR-T; Cell therapy; Solid tumors; TCR-T; TIL; TILs; Thérapie cellulaire; Tumeurs solides.

Publication types

  • Review

MeSH terms

  • Antigens, Differentiation / immunology
  • Antigens, Neoplasm / immunology
  • Cell Engineering
  • Humans
  • Immunotherapy, Adoptive / methods*
  • Lymphocytes, Tumor-Infiltrating / cytology
  • Lymphocytes, Tumor-Infiltrating / immunology
  • Lymphocytes, Tumor-Infiltrating / transplantation*
  • Neoplasms / immunology
  • Neoplasms / therapy*
  • Receptors, Antigen, T-Cell*
  • Receptors, Chimeric Antigen / immunology*
  • Tumor Microenvironment / immunology

Substances

  • Antigens, Differentiation
  • Antigens, Neoplasm
  • Receptors, Antigen, T-Cell
  • Receptors, Chimeric Antigen