Genetic Modification Strategies to Enhance CAR T Cell Persistence for Patients With Solid Tumors

Front Immunol. 2019 Feb 15:10:218. doi: 10.3389/fimmu.2019.00218. eCollection 2019.

Abstract

Immunotherapy with chimeric antigen receptor (CAR) T cells offers a promising method to improve cure rates and decrease morbidities for patients with cancer. In this regard, CD19-specific CAR T cell therapies have achieved dramatic objective responses for a high percent of patients with CD19-positive leukemia or lymphoma. Most patients with solid tumors however, have experienced transient or no benefit from CAR T cell therapies. Novel strategies are therefore needed to improve CAR T cell function for patients with solid tumors. One obstacle for the field is limited CAR T cell persistence after infusion into patients. In this review we highlight genetic engineering strategies to improve CAR T cell persistence for enhancing antitumor activity for patients with solid tumors.

Keywords: CAR T cell; genetic modification; immunotherapy; persistence; solid tumor.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't
  • Review

MeSH terms

  • Animals
  • Genetic Engineering
  • Helminth Proteins / genetics*
  • Humans
  • Immunotherapy, Adoptive / methods*
  • Neoplasms / immunology
  • Neoplasms / therapy*
  • Receptors, Chimeric Antigen / genetics*
  • T-Lymphocytes / immunology*
  • T-Lymphocytes / transplantation

Substances

  • Helminth Proteins
  • Receptors, Chimeric Antigen
  • TCEN49 protein, Dugesia tigrina