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PMID: 14768041 Published · ppublish English Journal Article

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

European journal of immunology ·Vol. 34 ·No. 2 ·2004-02-00 ·Pages 366-76

Thornton AM, Piccirillo CA, Shevach EM

Abstract

The in vivo differentiation/survival of CD4(+)CD25(+) T suppressor cells is dependent on IL-2 and CD28-mediated costimulatory signals. To determine the cytokine and costimulatory requirements for CD25(+) T cells in vitro, we established a two-stage culture system where CD25(+) T cells were activated in a primary culture. In the subsequent culture, activated CD4(+)CD25(+) cells were then mixed with responders in order to assess their suppressor function. Pre-culture of CD25(+) T cells with anti-CD3 alone resulted in poor survival and minimal induction of suppressor activity. Pre-culture in the presence of anti-CD3 and IL-2 or IL-4, but not IL-6, IL-7, IL-9, IL-10 or IL-15, resulted in proliferation of the CD25(+) cells and induction of potent suppressor function. Inhibition of the interaction of CD28 or cytotoxic T lymphocyte-associated antigen-4 (CTLA-4) with CD80/CD86 in the pre-culture of CD4(+)CD25(+) cells did not prevent the induction of suppressor function. Furthermore, the inhibition of costimulatory signals did not inhibit the ability of fresh CD25(+) T cells to inhibit CD8(+) responders under conditions where activation of the responders was independent of CD80/CD86. These studies support the view that activation of CD25(+) T cells requires IL-2/IL-4 for their survival/differentiation into effector cells, but is independent of CD28/CTLA-4-mediated costimulation.

MeSH Terms
Animals Antigens, CD Antigens, Differentiation/immunology CD28 Antigens/immunology CD4 Antigens/immunology CTLA-4 Antigen Cell Division/immunology Clonal Anergy Female Interleukin-2/immunology Lymphocyte Activation/immunology Mice Mice, Inbred BALB C Mice, Knockout Mice, Transgenic Receptors, Interleukin-2/immunology T-Lymphocytes, Regulatory/cytology,immunology
Chemicals
Antigens, CD Antigens, Differentiation CD28 Antigens CD4 Antigens CTLA-4 Antigen Ctla4 protein, mouse Interleukin-2 Receptors, Interleukin-2
Authors & Affiliations
3 authors, click to expand affiliations / ORCID
Thornton Angela M
Laboratory of Immunology, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Bethesda 20892-1892, USA. athornton@niaid.nih.gov
Piccirillo Ciriaco A
Shevach Ethan M
Article Info
Journal
European journal of immunology
Abbr.
Eur J Immunol
ISSN
0014-2980
Published
2004-02-00
Pages
366-76
Language
English
Region
Germany
NLM ID
1273201
Subset
IM
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