High CAR intensity of expression confers enhanced antitumor effect against lymphoma without functional exhaustion

Cancer Gene Ther. 2023 Jan;30(1):51-61. doi: 10.1038/s41417-022-00518-6. Epub 2022 Aug 29.

Abstract

Identifying factors that ameliorates clinical outcomes following CART therapy represents an unmet need. We hypothesized that CAR expression level would have a significant impact on CART efficacy and tested this with CAR30+ TSCM-LIKE enriched cells. By sorting T-cells according to CAR mean fluorescence intensity in two markedly different populations (CARHI and CARLO), we showed that a high CAR expression enhances antitumor efficacy in vitro, that is sustained after sequential re-exposures to tumor cells and is not associated with T-cell exhaustion or differentiation. Furthermore, we found a correlation between high surface CAR expression and antitumor effect with CAR19+ T-cells, thus validating our findings with CAR30. Definitive proof of CARHI T-cells improved antitumor efficacy was demonstrated in a human Hodgkin's lymphoma xenograft mouse model, where CAR30-TSCM-LIKE enriched products with high intensity of CAR expression achieved superior tumor control in vivo and longer survival than those with a low intensity of CAR expression. Our data suggest that modulation of CAR intensity of expression represents an additional strategy to increase CART therapy clinical efficacy.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Humans
  • Immunotherapy, Adoptive
  • Lymphoma* / genetics
  • Lymphoma* / therapy
  • Mice
  • Neoplasms* / therapy
  • T-Lymphocytes / pathology
  • Treatment Outcome
  • Xenograft Model Antitumor Assays