Engineered T cells: the promise and challenges of cancer immunotherapy

Nat Rev Cancer. 2016 Aug 23;16(9):566-81. doi: 10.1038/nrc.2016.97.

Abstract

The immune system evolved to distinguish non-self from self to protect the organism. As cancer is derived from our own cells, immune responses to dysregulated cell growth present a unique challenge. This is compounded by mechanisms of immune evasion and immunosuppression that develop in the tumour microenvironment. The modern genetic toolbox enables the adoptive transfer of engineered T cells to create enhanced anticancer immune functions where natural cancer-specific immune responses have failed. Genetically engineered T cells, so-called 'living drugs', represent a new paradigm in anticancer therapy. Recent clinical trials using T cells engineered to express chimeric antigen receptors (CARs) or engineered T cell receptors (TCRs) have produced stunning results in patients with relapsed or refractory haematological malignancies. In this Review we describe some of the most recent and promising advances in engineered T cell therapy with a particular emphasis on what the next generation of T cell therapy is likely to entail.

Publication types

  • Review

MeSH terms

  • Antigen Presentation
  • Antigens, CD19 / immunology
  • Antigens, Neoplasm / immunology
  • Clinical Trials as Topic
  • Costimulatory and Inhibitory T-Cell Receptors / genetics
  • Costimulatory and Inhibitory T-Cell Receptors / immunology
  • Cytokines / metabolism
  • Forecasting
  • Gene Editing
  • Gene Transfer Techniques
  • Genetic Engineering
  • HLA Antigens / immunology
  • Hematologic Neoplasms / immunology
  • Hematologic Neoplasms / therapy
  • Humans
  • Immunotherapy, Adoptive / adverse effects
  • Immunotherapy, Adoptive / methods*
  • Immunotherapy, Adoptive / trends
  • Models, Immunological
  • Neoplasms / immunology
  • Neoplasms / therapy*
  • Receptors, Antigen, T-Cell / genetics
  • Receptors, Antigen, T-Cell / immunology*
  • Recombinant Fusion Proteins / genetics
  • Recombinant Fusion Proteins / immunology
  • Syndrome
  • T-Cell Antigen Receptor Specificity
  • T-Lymphocyte Subsets / immunology*
  • T-Lymphocyte Subsets / transplantation
  • Tumor Escape
  • Tumor Microenvironment / immunology

Substances

  • Antigens, CD19
  • Antigens, Neoplasm
  • CD19 molecule, human
  • Costimulatory and Inhibitory T-Cell Receptors
  • Cytokines
  • HLA Antigens
  • Receptors, Antigen, T-Cell
  • Recombinant Fusion Proteins