Tim-3: A co-receptor with diverse roles in T cell exhaustion and tolerance

Semin Immunol. 2019 Apr:42:101302. doi: 10.1016/j.smim.2019.101302.

Abstract

T cell inhibitory co-receptors play a crucial role in maintaining the balance between physiologic immune responses and maladaptive ones. T cell immunoglobulin and mucin domain-containing-3 (Tim-3) is a unique inhibitory co-receptor in that its expression is chiefly restricted to interferon (IFN)γ-producing CD4+ and CD8+ T cells. Early reports firmly established its importance in maintaining peripheral tolerance in transplantation and autoimmunity. However, it has become increasingly clear that Tim-3 expression on T cells, together with other check-point molecules, in chronic infections and cancers can hinder productive immune responses. In this review, we outline what is currently known about the regulation of Tim-3 expression, its ligands and signaling. We discuss both its salutary and deleterious function in immune disorders, as well as the T cell-extrinsic and -intrinsic factors that regulate its function.

Keywords: Autoimmunity; Cancer; Coreceptor; Experimental autoimmune encephalomyelitis; HIV-1; Immune checkpoint; Inflammation; T cell; T cell exhaustion; Tim-3.

Publication types

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

MeSH terms

  • Animals
  • Autoimmunity
  • Hepatitis A Virus Cellular Receptor 2 / chemistry
  • Hepatitis A Virus Cellular Receptor 2 / immunology*
  • Humans
  • Immune Tolerance*
  • Infections / immunology
  • Ligands
  • Neoplasms / immunology
  • Protein Conformation
  • T-Lymphocytes / immunology*

Substances

  • Hepatitis A Virus Cellular Receptor 2
  • Ligands