Cytokines affecting CD4(+) T regulatory cells in transplant tolerance. Interleukin-4 does not maintain alloantigen specific CD4(+)CD25(+) Treg

Transpl Immunol. 2013 Dec;29(1-4):51-9. doi: 10.1016/j.trim.2013.10.003. Epub 2013 Oct 16.

Abstract

IL-4 is thought to promote induction of transplantation tolerance and alloantigen-specific CD4(+)CD25(+) T regulatory cells (Treg). This study examined the effect of IL-4 on the induction and maintenance of the CD4(+) T regulatory cells (Treg) that mediate transplantation tolerance. Tolerance was induced in DA rats with PVG heterotopic cardiac allografts by a short course of cyclosporine. Naïve and tolerant lymphocytes, including the CD4(+) and CD4(+)CD25(+) T cell subsets, were assayed in mixed lymphocyte cultures with or without recombinant (r)IL-4 or other cytokines. The proliferation, cell surface and cytokine phenotype of these cells was examined, as was their capacity to adoptively transfer tolerance. rIL-4 enhanced the proliferation of naïve and tolerant lymphoid cells, including CD4(+) and CD4(+)CD25(+) T cells, but this was not alloantigen specific. Naïve or tolerant CD4(+) T cells cultured with rIL-4 and donor PVG antigen effected rapid graft rejection, even though before culture tolerant CD4(+) T cells transferred antigen-specific tolerance. These rIL-4 cultured CD4(+) T cells had a phenotype consistent with activated CD4(+)CD25(+)FoxP3(-) Th2 cells. While naïve natural CD4(+)CD25(+) T cells (nTreg) cultured with alloantigen and rIL-4 had enhanced proliferation and capacity to suppress rejection in vivo, the culture of tolerant CD4(+)CD25(+) T cells with alloantigen and rIL-4 could not sustain their proliferation against specific donor, nor their capacity to transfer tolerance to specific donor allograft. Thus, IL-4 promotes both regulatory and effector T cells early in the immune response, but once alloimmune tolerance is established, IL-4 promoted the activation of effector cells to mediate rejection and did not support alloantigen-specific Treg that could transfer specific tolerance.

Keywords: CD4(+)CD25(+)FoxP3(+) Treg; CPM; ConAsup; Counts per minute; IFN-γ; IFN-γ receptor; IFNGR; IL; IL-5 receptor alpha, specific for IL-5 binding; IL-5Rα; Interferon-gamma; Interleukin; Interleukin 4; MLC; Mixed lymphocyte culture; Natural T regulatory cells (CD4(+)CD25(+)FoxP3(+) T cell); Recombinant rat interleukin; Regulatory T cell; Supernatant from concanavalin A activated spleen cells; T regulatory cells induced from CD4(+)CD25(−) T cells; Th2 response; Transplantation tolerance; Ts1; Ts2; iTreg; nTreg; nTreg activated by IL-2 and alloantigen; nTreg activated by IL-4 and alloantigen; rIL.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Allografts
  • Animals
  • Cell Proliferation / drug effects
  • Graft Rejection / immunology*
  • Graft Rejection / pathology
  • Graft Rejection / prevention & control
  • Graft Survival / drug effects
  • Graft Survival / immunology
  • Interleukin-4 / immunology
  • Interleukin-4 / pharmacology*
  • Isoantigens / immunology*
  • Rats
  • Rats, Inbred Lew
  • T-Lymphocytes, Regulatory / immunology*
  • T-Lymphocytes, Regulatory / pathology
  • Th2 Cells / immunology
  • Th2 Cells / pathology
  • Transplantation Tolerance / drug effects*

Substances

  • Isoantigens
  • Interleukin-4