New cell sources for T cell engineering and adoptive immunotherapy

Cell Stem Cell. 2015 Apr 2;16(4):357-66. doi: 10.1016/j.stem.2015.03.011.

Abstract

The promising clinical results obtained with engineered T cells, including chimeric antigen receptor (CAR) therapy, call for further advancements to facilitate and broaden their applicability. One potentially beneficial innovation is to exploit new T cell sources that reduce the need for autologous cell manufacturing and enable cell transfer across histocompatibility barriers. Here we review emerging T cell engineering approaches that utilize alternative T cell sources, which include virus-specific or T cell receptor-less allogeneic T cells, expanded lymphoid progenitors, and induced pluripotent stem cell (iPSC)-derived T lymphocytes. The latter offer the prospect for true off-the-shelf, genetically enhanced, histocompatible cell therapy products.

Publication types

  • Review

MeSH terms

  • Animals
  • Cell Engineering / methods*
  • Genetic Engineering
  • Histocompatibility
  • Humans
  • Immunologic Deficiency Syndromes / immunology
  • Immunologic Deficiency Syndromes / therapy*
  • Immunotherapy, Adoptive*
  • Induced Pluripotent Stem Cells / immunology*
  • Induced Pluripotent Stem Cells / transplantation
  • Lymphoid Progenitor Cells / immunology*
  • Lymphoid Progenitor Cells / transplantation
  • Receptors, Antigen, T-Cell / genetics
  • Recombinant Fusion Proteins / genetics
  • T-Lymphocytes / immunology*
  • T-Lymphocytes / transplantation

Substances

  • Receptors, Antigen, T-Cell
  • Recombinant Fusion Proteins