作者
Li-Tzu Yeh, Shi-Chuen Miaw, Ming-Hong Lin, Feng-Cheng Chou, Shing-Jia Shieh, Yi-Ping Chuang, Shih-Hua Lin, Deh-Ming Chang, Huey-Kang Sytwu
发表日期
2013/7/15
期刊
The Journal of Immunology
卷号
191
期号
2
页码范围
594-607
出版商
American Association of Immunologists
简介
Ptpn22 encodes PEST domain–enriched tyrosine phosphatase (Pep), which negatively regulates TCR proximal signaling and is strongly associated with a variety of autoimmune diseases in humans. The net effect of Pep on the balance of immunity and tolerance is uncertain because of the simultaneous inhibition of TCR-mediated signaling of effector and regulatory T cells (T regs). In this study, we generated transgenic NOD mice that overexpressed Pep in T cells. The transgenic mice had a significantly lower incidence of spontaneous autoimmune diabetes, which was accompanied by fewer IFN-γ–producing T cells, and an increased ratio of CD4+ Foxp3+ T regs to CD4+ IFN-γ+ or to CD8+ IFN-γ+ T cells, respectively, in pancreatic islets. Transgenic T cells showed markedly decreased TCR-mediated effector cell responses such as proliferation and Th1 differentiation. By contrast, the inhibitory effect of transgenic …
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