4.5 Article

Critical role of IL-2 and TGF-β in generation, function and stabilization of Foxp3+CD4+ Treg

期刊

EUROPEAN JOURNAL OF IMMUNOLOGY
卷 38, 期 4, 页码 912-915

出版社

WILEY
DOI: 10.1002/eji.200738109

关键词

Foxp3; IL-2; IL-6; Regulatory cells; TGF-beta

资金

  1. Nora Eccles Treadwell Foundation
  2. BD Biosciences and ExCell Therapeutics
  3. Arthritis Foundation
  4. Arthritis National Research Foundation
  5. Clinical Research Feasibility Fund
  6. James H. Zumberge Faculty Research and Innovation Fund

向作者/读者索取更多资源

CD4(+)Foxp3(+) Treg consist of two indistinguishable subsets induced in either the thymus or the periphery. In addition to their suppressive activities, IL-6 can convert natural Treg to pro-inflammatory IL-17-producing cells, but those induced with IL-2 and TGF-beta remain Treg. Unlike mouse CD4(+)CD25(-) cells, which rapidly become polyclonal Foxp3(+)CD25(+) Treg when activated appropriately with IL-2 and TGF-beta, human T cells require multiple stimulations to become similar suppressor cells.

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