Augmenting CAR T Cell Functions with LIGHT. Academic Article uri icon

Overview

abstract

  • Chimeric antigen receptor (CAR) T-cell therapy has resulted in remarkable clinical success in the treatment of B-cell malignancies. However, its clinical efficacy in solid tumors is limited, primarily by target antigen heterogeneity. To overcome antigen heterogeneity, we developed CAR T cells that overexpress LIGHT, a ligand of both LTβR on cancer cells and HVEM on immune cells. LIGHT-expressing CAR T cells displayed both antigen-directed cytotoxicity mediated by the CAR and antigen-independent killing mediated through the interaction of LIGHT with LTβR on cancer cells. Moreover, CAR T cells expressing LIGHT had immunostimulatory properties that improved the cells' proliferation and cytolytic profile. These data indicate that LIGHT-expressing CAR T cells may provide a way to eliminate antigen-negative tumor cells to prevent antigen-negative disease relapse.

publication date

  • July 3, 2024

Research

keywords

  • Immunotherapy, Adoptive
  • Receptors, Chimeric Antigen
  • T-Lymphocytes
  • Tumor Necrosis Factor Ligand Superfamily Member 14

Identity

Digital Object Identifier (DOI)

  • 10.1158/2326-6066.CIR-24-0246

PubMed ID

  • 38959337