Activation-induced surface proteins in the identification of antigen-responsive CD4 T cells

Immunol Lett. 2020 Mar:219:1-7. doi: 10.1016/j.imlet.2019.12.006. Epub 2019 Dec 24.

Abstract

Identification of antigen specificity of CD4 T cells is instrumental in understanding adaptive immune responses in health and disease. The high diversity of CD4 T cell repertoire combined with the functional heterogeneity of the compartment poses a challenge to the assessment of CD4 T cell responses. In spite of that, multiple technologies allow direct or indirect interrogation of antigen specificity of CD4 T cells. In the last decade, multiple surface proteins have been established as cytokine-independent surrogates of in vitro CD4 T cell activation, and have found applications in the live identification and isolation of antigen-responsive CD4 T cells. Here we review the current knowledge of the surface proteins that permit identification of viable antigen-responsive CD4 T cells with high specificity, including those capable of identifying specialized CD4 T subsets such as germinal center follicular helper T cells and CD4 regulatory T cells.

Keywords: 4-1BB; Antigen; CD134; CD137; CD154; CD274; CD4; CD40L; OX40; PD-L1; T-Cells.

Publication types

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

MeSH terms

  • Animals
  • Antigens / immunology*
  • Biomarkers
  • CD4-Positive T-Lymphocytes / immunology*
  • CD4-Positive T-Lymphocytes / metabolism*
  • Cell Communication
  • Gene Expression
  • Homeostasis
  • Humans
  • Immunomodulation
  • Immunophenotyping
  • Lymphocyte Activation / immunology*
  • Membrane Proteins / genetics
  • Membrane Proteins / metabolism*
  • Signal Transduction
  • T-Lymphocyte Subsets / immunology
  • T-Lymphocyte Subsets / metabolism

Substances

  • Antigens
  • Biomarkers
  • Membrane Proteins