TH-17 cells in the circle of immunity and autoimmunity

被引:0
|
作者
Estelle Bettelli
Mohamed Oukka
Vijay K Kuchroo
机构
[1] Estelle Bettelli and Vijay K. Kuchroo are in the Center for Neurologic Diseases,
[2] Brigham and Women's Hospital,undefined
[3] Boston,undefined
[4] Massachusetts 02115,undefined
[5] USA.,undefined
[6] Mohamed Oukka is in the Center for Neurologic Diseases,undefined
[7] Brigham and Women's Hospital,undefined
[8] Harvard Medical School,undefined
[9] Cambridge,undefined
[10] Massachusetts 02139,undefined
[11] USA.,undefined
来源
Nature Immunology | 2007年 / 8卷
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摘要
CD4+ effector T cells have been categorized into two subsets: T helper type 1 (TH1) and TH2. Another subset of T cells that produce interleukin 17 (IL-17; 'TH-17 cells') has been identified that is highly proinflammatory and induces severe autoimmunity. Whereas IL-23 serves to expand previously differentiated TH-17 cell populations, IL-6 and transforming growth factor-β (TGF-β) induce the differentiation of TH-17 cells from naive precursors. These data suggest a dichotomy between CD4+ regulatory T cells positive for the transcription factor Foxp3 and TH-17 cells: TGF-β induces Foxp3 and generates induced regulatory T cells, whereas IL-6 inhibits TGF-β-driven Foxp3 expression and together with TGF-β induces TH-17 cells. Emerging data regarding TH-17 cells suggest a very important function for this T cell subset in immunity and disease.
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页码:345 / 350
页数:5
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