Photoswitchable CAR-T Cell Function In Vitro and In Vivo via a Cleavable Mediator

Cell Chem Biol. 2021 Jan 21;28(1):60-69.e7. doi: 10.1016/j.chembiol.2020.10.004. Epub 2020 Oct 27.

Abstract

Chimeric antigen receptor (CAR)-T-based therapeutics are a breakthrough in cancer treatment; however, they are hampered by constitutive activation, which leads to worrisome side effects. Engineering CAR-T cells to be as tightly controllable as possible remains a topic of ongoing investigation. Here, we report a photoswitchable approach that uses a mediator for the at-will regulation of CAR-T cells. This mediator carries dual folate and fluorescein isothiocyanate moieties tethered by an ortho-nitrobenzyl ester photocleavable linker. CAR-T cells were shown to be highly cytotoxic to targeted cells only in the presence of the mediator and acted in a dose-dependent manner. The toxicity of CAR-T cells can be rapidly terminated by cleavage of the mediator, and the effects of CAR-T cells can be activated again by resupplementation with the mediator without compromising tumor therapy. The approach described here provides a direction for enhancing the controllability of CAR-T cells and can likely be applied in other immunotherapies.

Keywords: CAR-T cytotoxicity; cleavable mediator; fluorescein isothiocyanate; photoswitchable.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Cells, Cultured
  • Female
  • Mice
  • Mice, Inbred NOD
  • Mice, SCID
  • Neoplasms / immunology*
  • Neoplasms / therapy
  • Photochemical Processes
  • Receptors, Chimeric Antigen / immunology*
  • T-Lymphocytes / immunology*

Substances

  • Receptors, Chimeric Antigen