Optimization of T Cell Redirecting Strategies: Obtaining Inspirations From Natural Process of T Cell Activation

Front Immunol. 2021 Apr 26:12:664329. doi: 10.3389/fimmu.2021.664329. eCollection 2021.

Abstract

Chimeric antigen receptors (CARs) or bispecific antibodies (bsAbs) redirected T cell against tumors is one of the most promising immunotherapy approaches. However, insufficient clinical outcomes are still observed in treatments of both solid and non-solid tumors. Limited efficacy and poor persistence are two major challenges in redirected T cell therapies. The immunological synapse (IS) is a vital component during the T cell response, which largely determines the clinical outcomes of T cell-based therapies. Here, we review the structural and signaling characteristics of IS formed by natural T cells and redirected T cells. Furthermore, inspired by the elaborate natural T cell receptor-mediated IS, we provide potential strategies for higher efficacy and longer persistence of redirected T cells.

Keywords: T cell-based immunotherapy; bispecific antibody; chimeric antigen receptor; immunological synapse; metabolism.

Publication types

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

MeSH terms

  • Animals
  • Antibodies, Bispecific / chemistry
  • Antibodies, Bispecific / immunology
  • Antibodies, Bispecific / metabolism
  • Antigens, Neoplasm / immunology
  • Humans
  • Immunological Synapses / immunology
  • Immunological Synapses / metabolism
  • Immunotherapy, Adoptive / methods*
  • Lymphocyte Activation / immunology
  • Neoplasms / immunology
  • Neoplasms / therapy
  • Protein Binding
  • Receptors, Antigen, T-Cell / chemistry
  • Receptors, Antigen, T-Cell / immunology*
  • Receptors, Antigen, T-Cell / metabolism
  • Receptors, Chimeric Antigen / chemistry
  • Receptors, Chimeric Antigen / immunology*
  • Receptors, Chimeric Antigen / metabolism
  • Signal Transduction
  • Structure-Activity Relationship
  • T-Cell Antigen Receptor Specificity
  • T-Lymphocytes / immunology*
  • T-Lymphocytes / metabolism*

Substances

  • Antibodies, Bispecific
  • Antigens, Neoplasm
  • Receptors, Antigen, T-Cell
  • Receptors, Chimeric Antigen