Costimulation blockade in combination with IL-2 permits regulatory T cell sparing immunomodulation that inhibits autoimmunity

Nat Commun. 2022 Nov 9;13(1):6757. doi: 10.1038/s41467-022-34477-1.

Abstract

Blockade of CD28 costimulation with CTLA-4-Ig/Abatacept is used to dampen effector T cell responses in autoimmune and transplantation settings. However, a significant drawback of this approach is impaired regulatory T cell homeostasis that requires CD28 signaling. Therefore, strategies that restrict the effects of costimulation blockade to effector T cells would be advantageous. Here we probe the relative roles of CD28 and IL-2 in maintaining Treg. We find provision of IL-2 counteracts the regulatory T cell loss induced by costimulation blockade while minimally affecting the conventional T cell compartment. These data suggest that combining costimulation blockade with IL-2 treatment may selectively impair effector T cell responses while maintaining regulatory T cells. Using a mouse model of autoimmune diabetes, we show combined therapy supports regulatory T cell homeostasis and protects from disease. These findings are recapitulated in humanised mice using clinically relevant reagents and provide an exemplar for rational use of a second immunotherapy to offset known limitations of the first.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Abatacept / pharmacology
  • Autoimmunity
  • CD28 Antigens*
  • CTLA-4 Antigen
  • Immunomodulation
  • Interleukin-2 / pharmacology
  • Lymphocyte Activation
  • T-Lymphocytes, Regulatory*

Substances

  • CD28 Antigens
  • Interleukin-2
  • CTLA-4 Antigen
  • Abatacept