Stimulatory and Inhibitory Co-signals in Autoimmunity

Adv Exp Med Biol. 2019;1189:213-232. doi: 10.1007/978-981-32-9717-3_8.


Co-receptors cooperatively regulate the function of immune cells to optimize anti-infectious immunity while limiting autoimmunity by providing stimulatory and inhibitory co-signals. Among various co-receptors, those in the CD28/CTLA-4 family play fundamental roles in the regulation of lymphocytes by modulating the strength, quality, and/or duration of the antigen receptor signal. The development of the lethal lymphoproliferative disorder and various tissue-specific autoimmune diseases in mice deficient for CTLA-4 and PD-1, respectively, clearly demonstrates their pivotal roles in the development and the maintenance of immune tolerance. The recent success of immunotherapies targeting CTLA-4 and PD-1 in the treatment of various cancers highlights their critical roles in the regulation of cancer immunity in human. In addition, the development of multifarious autoimmune diseases as immune-related adverse events of anti-CTLA-4 and anti-PD-1/PD-L1 therapies and the successful clinical application of the CD28 blocking therapy using CTLA-4-Ig to the treatment of arthritis assure their crucial roles in the regulation of autoimmunity in human. Accumulating evidences in mice and humans indicate that genetic and environmental factors strikingly modify effects of the targeted inhibition and potentiation of co-signals. In this review, we summarize our current understanding of the roles of CD28, CTLA-4, and PD-1 in autoimmunity. Deeper understandings of the context-dependent and context-independent functions of co-signals are essential for the appropriate usage and the future development of innovative immunomodulatory therapies for a diverse array of diseases.

Keywords: Animal model; CD28; CTLA-4; Cancer immunotherapy; PD-1; SNV; Strain; Susceptibility; Tolerance; irAE.

Publication types

  • Review

MeSH terms

  • Animals
  • Autoimmunity*
  • CD28 Antigens / metabolism*
  • CTLA-4 Antigen / metabolism*
  • Humans
  • Immune Tolerance
  • Immunotherapy
  • Mice
  • Programmed Cell Death 1 Receptor / metabolism*


  • CD28 Antigens
  • CTLA-4 Antigen
  • Programmed Cell Death 1 Receptor