Cyclosporin A increases IFN-gamma production by T cells when co-stimulated through CD28

Eur J Immunol. 1998 May;28(5):1481-91. doi: 10.1002/(SICI)1521-4141(199805)28:05<1481::AID-IMMU1481>3.0.CO;2-4.

Abstract

Despite its calcineurin-inhibiting properties, cyclosporin A (CsA) can not inhibit IL-2 production when T cells are co-stimulated by CD80/CD86 on the antigen-presenting cells. We studied the in vitro effect of CsA on IFN-gamma production. Anti-CD3 monoclonal antibody (mAb) was used as the primary stimulus for activation of purified human T cells. A stimulating anti-CD28 mAb, or CD80 or CD86 on stably transfected P815 cells, provided the co-stimulatory signal. IL-2 production was hardly affected by CsA under these stimulating conditions, while IFN-gamma (at the protein and mRNA level) was markedly stimulated by CsA. The use of anti-CD3 or phorbol 12-myristate 13-acetate with ionomycin as the primary stimulus, together with costimulation through either CD28 or CD2 using transfectants with the appropriate ligands, allowed us to demonstrate that the resistance of IFN-gamma production to inhibition by CsA required both CD3 and CD28 triggering. Inhibition of IL-10 production, and to a lesser degree of IL-4 production, by CD4+ cells was responsible for the enhancement of IFN-gamma production in the presence of CsA. In conclusion, IFN-gamma production by CD28-co-stimulated CD4+ T cells is resistant to inhibition by CsA and can even be facilitated by CsA as a result of removing a negative regulatory signal which is mainly IL-10 mediated. This finding might have implications for immunosuppressive strategies based upon the use of CsA.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adjuvants, Immunologic / pharmacology*
  • Adjuvants, Immunologic / physiology*
  • Animals
  • CD28 Antigens / physiology*
  • CD3 Complex / physiology
  • CD4-Positive T-Lymphocytes / metabolism
  • Cyclosporine / pharmacology*
  • Drug Resistance
  • Humans
  • Interferon-gamma / biosynthesis*
  • Interferon-gamma / genetics
  • Interleukin-10 / antagonists & inhibitors
  • Interleukin-10 / biosynthesis
  • Interleukin-2 / physiology
  • Interleukin-4 / antagonists & inhibitors
  • Interleukin-4 / biosynthesis
  • Lymphocyte Activation* / drug effects
  • Mast-Cell Sarcoma
  • Mice
  • RNA, Messenger / drug effects
  • Signal Transduction / drug effects
  • Signal Transduction / immunology
  • T-Lymphocytes / immunology
  • T-Lymphocytes / metabolism*
  • Tumor Cells, Cultured

Substances

  • Adjuvants, Immunologic
  • CD28 Antigens
  • CD3 Complex
  • Interleukin-2
  • RNA, Messenger
  • Interleukin-10
  • Interleukin-4
  • Interferon-gamma
  • Cyclosporine