CARTs for Solid Tumors: Feasible or Infeasible?

Oncol Res Treat. 2017;40(9):540-546. doi: 10.1159/000477095. Epub 2017 Aug 17.

Abstract

Adoptive transfer of chimeric antigen receptor-engineered T cells (CARTs) is a novel approach to cancer therapy as CARTs combine with the antigen specificity of an antibody and the activating functions of T lymphocytes. Recent results from preclinical and clinical trials with CARTs for B-cell malignancies are exciting, although different groups selected different tumor-associated antigens, binding domains, and signal domains, which make up the chimeric antigen receptor (CAR) configuration. However, there are few clinical trials with CARTs for solid tumors compared to hematologic malignancies. In this brief review, we discuss the basic principles of CAR design and clinical studies of CARTs for solid tumors.

Keywords: Chimeric antigen receptor; Immunotherapy; Solid tumor; T cell.

Publication types

  • Review

MeSH terms

  • Animals
  • Antibodies, Monoclonal / immunology*
  • Antibodies, Monoclonal / therapeutic use*
  • Cell Engineering*
  • Clinical Trials as Topic
  • Epitopes / immunology
  • Humans
  • Immunotherapy, Adoptive / methods*
  • Neoplasms / immunology*
  • Neoplasms / therapy*
  • Receptors, Antigen, T-Cell / immunology*
  • Recombinant Fusion Proteins / immunology
  • Recombinant Fusion Proteins / therapeutic use*
  • T-Lymphocytes / immunology*
  • T-Lymphocytes / transplantation

Substances

  • Antibodies, Monoclonal
  • Epitopes
  • Receptors, Antigen, T-Cell
  • Recombinant Fusion Proteins