期刊
JOURNAL OF IMMUNOLOGY
卷 202, 期 6, 页码 1693-1703出版社
AMER ASSOC IMMUNOLOGISTS
DOI: 10.4049/jimmunol.1801051
关键词
-
类别
资金
- National Natural Science Foundation of China [81601424, 81701612, 31470881, 91842304]
- Natural Science Foundation of Jiangsu [BK20150533, BK20170563]
- Jiangsu Province's Key Medical Talents Program [ZDRCB2016018]
- China Postdoctoral Science Foundation [2016M590423, 2017T100336]
- Summit of the Six Top Talents Program of Jiangsu Province [2017-YY-006]
- Young Talent Cultivation Program of Jiangsu University
- Hong Kong Croucher Foundation [260960116]
- Primary Research and Development Plan of Zhenjiang [SH2017008]
- General Research Fund
- Hong Kong Research Grants Council [17114515, 17149716]
- Chinese National Key Technology R&D Program, Ministry of Science and Technology [2017YFC0907601, 2017YFC0907605]
Although the expansion of myeloid-derived suppressor cells (MDSCs) has been reported in autoimmune disorders, it is largely unclear how MDSCs contribute to the development of primary Sjogren syndrome (pSS). In this study, we found significantly increased MDSCs with gradually diminished suppressive capacity during disease development in mice with experimental Sjogren syndrome (ESS). The ligand for glucocorticoid-induced TNFR family-related protein (GITRL) was increased along ESS progression, whereas the increased GITRL was found to attenuate the immunosuppressive function of MDSCs. Moreover, blocking GITR signal in MDSCs significantly restored their immunosuppressive function and alleviated ESS progression in mice. In pSS patients, expanded MDSCs were found to express low levels of arginase. Significantly increased serum GITRL levels were closely correlated with patients with higher Sjogren syndrome disease activity index. Furthermore, treatment with recombinant GITRL markedly reduced the immunosuppressive function of human MDSCs. Together, our studies have demonstrated a critical role of GITRL in modulating the suppressive function of MDSCs, which may facilitate the validation of GITRL as a therapeutic target for the treatment of pSS.
作者
我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。
推荐
暂无数据