A promising antitumor method: Targeting CSC with immune cells modified with CAR

Front Immunol. 2022 Aug 11:13:937327. doi: 10.3389/fimmu.2022.937327. eCollection 2022.

Abstract

Tumors pose a great threat to human health; as a subgroup of tumor cells, cancer stem cells (CSCs) contribute to the genesis, development, metastasis, and recurrence of tumors because of their enhanced proliferation and multidirectional differentiation. Thus, a critical step in tumor treatment is to inhibit CSCs. Researchers have proposed many methods to inhibit or reduce CSCs, including monoclonal antibodies targeting specific surface molecules of CSCs, signal pathway inhibitors, and energy metabolic enzyme inhibitors and inducing differentiation therapy. Additionally, immunotherapy with immune cells engineered with a chimeric antigen receptor (CAR) showed favorable results. However, there are few comprehensive reviews in this area. In this review, we summarize the recent CSC targets used for CSC inhibition and the different immune effector cells (T cells, natural killer (NK) cells, and macrophages) which are engineered with CAR used for CSC therapy. Finally, we list the main challenges and options in targeting CSC with CAR-based immunotherapy. The design targeting two tumor antigens (one CSC antigen and one mature common tumor antigen) should be more reasonable and practical; meanwhile, we highlight the potential of CAR-NK in tumor treatment.

Keywords: CAR; CAR-NK; CSC; immunotherapy; targeted strategy.

Publication types

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

MeSH terms

  • Antigens, Neoplasm
  • Humans
  • Immunotherapy
  • Killer Cells, Natural
  • Neoplasms*
  • Receptors, Chimeric Antigen*
  • T-Lymphocytes

Substances

  • Antigens, Neoplasm
  • Receptors, Chimeric Antigen