Identification, selection, and expansion of non-gene modified alloantigen-reactive Tregs for clinical therapeutic use

Cell Immunol. 2020 Nov:357:104214. doi: 10.1016/j.cellimm.2020.104214. Epub 2020 Sep 9.

Abstract

Transplantation is limited by the need for life-long pharmacological immunosuppression, which carries significant morbidity and mortality. Regulatory T cell (Treg) therapy holds significant promise as a strategy to facilitate immunosuppression minimization. Polyclonal Treg therapy has been assessed in a number of Phase I/II clinical trials in both solid organ and hematopoietic transplantation. Attention is now shifting towards the production of alloantigen-reactive Tregs (arTregs) through co-culture with donor antigen. These allospecific cells harbour potent suppressive function and yet their specificity implies a theoretical reduction in off-target effects. This review will cover the progress in the development of arTregs including their potential application for clinical use in transplantation, the knowledge gained so far from clinical trials of Tregs in transplant patients, and future directions for Treg therapy.

Keywords: Alloantigen-reactive Tregs; Cellular therapy; Clinical trials; Regulatory T cells; Transplantation; polyTregs.

Publication types

  • Research Support, Non-U.S. Gov't
  • Review

MeSH terms

  • Animals
  • Graft Rejection / immunology
  • Humans
  • Immune Tolerance / immunology
  • Immunosuppression Therapy / methods
  • Isoantigens / immunology
  • Isoantigens / therapeutic use*
  • T-Lymphocytes, Regulatory / immunology*
  • T-Lymphocytes, Regulatory / transplantation*
  • Transplantation Tolerance / immunology

Substances

  • Isoantigens