Diabetes is not prevented by Foxp3-transduced CD4(+)T cells under the IL-12Rbeta2 promoter control.

Diabetes is not prevented by Foxp3-transduced CD4(+)T cells under the IL-12Rbeta2 promoter control.
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IL-12Rbeta2启动子控制下的Foxp3转导的CD4(+)T细胞不能预防糖尿病。

DOI:
10.1016/j.molimm.2008.05.016
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发表时间:
2008-08
影响因子:
3.6
通讯作者:
--
中科院分区:
医学3区
文献类型:
--
作者:

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Our previous studies have shown that Foxp3 under the control of IFN-γ promoter (IγP-Foxp3) converts pathogenic CD4+Th1 cells into regulatory T cells (Tregs), which control diabetes in non-obese diabetic (NOD) mice. Here, we tested the other hypothesis that transient expression of Foxp3 as controlled by the transient expression of IL-12Rβ2 during Th1 cell derivation is sufficient to convert cells to Tregs. Foxp3, under the control of IL-12Rβ2 promoter (Iβ2P), was lentivirally transduced into naïve CD4+T cells from NOD mice. Iβ2P-Foxp3-transduced CD4+T cells could not effectively suppress the incidence of diabetes when transferred into NOD mice. Furthermore, we found that Iβ2P-Foxp3-transduced CD4+T cells, stimulated by a high dose of autoantigen, did not suppress CD4+T cell activation, produce CD4+Foxp3+Tregs, and up-regulate CTLA4 expression. These results suggest that Iβ2P cannot mediate Foxp3 to convert pathogenic CD4+Th1 cells into Tregs which control diabetes in NOD mice.
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