Activation requirements for the induction of CD4+CD25+ T cell suppressor function

Angela M Thornton1, Ciriaco A Piccirillo, Ethan M Shevach

  • 1Laboratory of Immunology, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Bethesda 20892-1892, USA. athornton@niaid.nih.gov

Insights

Interleukin-2 (IL-2) and Interleukin-4 (IL-4) are crucial for the in vitro survival and differentiation of CD4(+)CD25(+) T suppressor cells. However, CD28 and CTLA-4 costimulatory signals are not required for their suppressor function.

Area of Science:

  • Immunology
  • Cell Biology
  • T cell differentiation

Background:

  • CD4(+)CD25(+) T suppressor cells are vital for immune regulation.
  • Their in vivo function relies on IL-2 and CD28 costimulation.
  • Understanding in vitro requirements is key to manipulating immune responses.

Purpose of the Study:

  • To elucidate the specific cytokine and costimulatory signals needed for CD4(+)CD25(+) T cell activation and suppressor function in vitro.
  • To investigate the roles of IL-2, IL-4, and costimulatory molecules (CD28, CTLA-4) in T suppressor cell development.

Main Methods:

  • A two-stage in vitro culture system was established.
  • CD4(+)CD25(+) T cells were activated in the primary culture.
  • Suppressor function was assessed by co-culturing activated cells with responder cells.

Main Results:

  • Pre-culture with anti-CD3 and IL-2 or IL-4 promoted CD4(+)CD25(+) T cell proliferation and potent suppressor function.
  • IL-6, IL-7, IL-9, IL-10, and IL-15 did not support suppressor activity.
  • Inhibition of CD28/CTLA-4 interactions did not impair suppressor function induction or activity.

Conclusions:

  • IL-2 and IL-4 are essential for the survival and differentiation of CD4(+)CD25(+) T cells into functional suppressor cells in vitro.
  • CD28/CTLA-4-mediated costimulation is not required for the induction or function of these T suppressor cells under the tested conditions.

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