Adoptive cellular immunotherapy for solid neoplasms beyond CAR-T

Mol Cancer. 2023 Feb 7;22(1):28. doi: 10.1186/s12943-023-01735-9.

Abstract

In recent decades, immune checkpoint blockade and chimeric antigen receptor T cell (CAR-T) therapy are two milestone achievements in clinical immunotherapy. However, both show limited efficacies in most solid neoplasms, which necessitates the exploration of new immunotherapeutic modalities. The failure of CAR-T and immune checkpoint blockade in several solid neoplasms is attributed to multiple factors, including low antigenicity of tumor cells, low infiltration of effector T cells, and diverse mechanisms of immunosuppression in the tumor microenvironment. New adoptive cell therapies have been attempted for solid neoplasms, including TCR-T, CAR-natural killer cells (CAR-NK), and CAR-macrophages (CAR-M). Compared to CAR-T, these new adoptive cell therapies have certain advantages in treating solid neoplasms. In this review, we summarized the 40-year evolution of adoptive cell therapies, then focused on the advances of TCR-T, CAR-NK, and CAR-M in solid neoplasms and discussed their potential clinical applications.

Keywords: Adoptive cell therapy; Chimeric antigen receptor; Immune checkpoint; Macrophage; Natural killer cell; TCR.

Publication types

  • Review
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Humans
  • Immune Checkpoint Inhibitors
  • Immunotherapy
  • Immunotherapy, Adoptive
  • Neoplasms* / therapy
  • Receptors, Antigen, T-Cell
  • Receptors, Chimeric Antigen*
  • Tumor Microenvironment

Substances

  • Receptors, Chimeric Antigen
  • Receptors, Antigen, T-Cell
  • Immune Checkpoint Inhibitors