CD4+CD25+ Immunoregulatory T Cells Suppress Polyclonal T Cell Activation In Vitro by Inhibiting Interleukin 2 Production

TLDR

Peripheral tolerance may be maintained by regulatory T cells that prevent activation of autoreactive T cells recognizing tissue‑specific antigens. The study aimed to analyze the mechanism of action of CD4+CD25+ T cells. An in‑vitro model system was established that mimics the in‑vivo function of these cells. CD4+CD25+ T cells suppress responder T‑cell proliferation by inhibiting IL‑2 production in a contact‑dependent, TCR‑activated manner that can be reversed by exogenous IL‑2 or anti‑CD28, and they do not acquire suppressor activity when CD25 is induced on CD25‑ cells, supporting their role as a distinct professional suppressor lineage.

Abstract

Peripheral tolerance may be maintained by a population of regulatory/suppressor T cells that prevent the activation of autoreactive T cells recognizing tissue-specific antigens. We have previously shown that CD4+CD25+ T cells represent a unique population of suppressor T cells that can prevent both the initiation of organ-specific autoimmune disease after day 3 thymectomy and the effector function of cloned autoantigen-specific CD4+ T cells. To analyze the mechanism of action of these cells, we established an in vitro model system that mimics the function of these cells in vivo. Purified CD4+CD25+ cells failed to proliferate after stimulation with interleukin (IL)-2 alone or stimulation through the T cell receptor (TCR). When cocultured with CD4+CD25- cells, the CD4+CD25+ cells markedly suppressed proliferation by specifically inhibiting the production of IL-2. The inhibition was not cytokine mediated, was dependent on cell contact between the regulatory cells and the responders, and required activation of the suppressors via the TCR. Inhibition could be overcome by the addition to the cultures of IL-2 or anti-CD28, suggesting that the CD4+CD25+ cells may function by blocking the delivery of a costimulatory signal. Induction of CD25 expression on CD25- T cells in vitro or in vivo did not result in the generation of suppressor activity. Collectively, these data support the concept that the CD4+CD25+ T cells in normal mice may represent a distinct lineage of "professional" suppressor cells.