The role of T regulatory cells in immunopathogenesis of myasthenia gravis: implications for therapeutics

被引:36
|
作者
Alahgholi-Hajibehzad, Mahdi [1 ]
Kasapoglu, Pinar [1 ]
Jafari, Reza [2 ]
Rezaei, Nima [3 ,4 ,5 ]
机构
[1] Istanbul Univ, Dept Immunol, Inst Expt Med DETAE, Istanbul, Turkey
[2] Tabriz Univ Med Sci, Immunol Res Ctr, Tabriz, Iran
[3] Univ Tehran Med Sci, Childrens Med Ctr, Res Ctr Immunodeficiencies, Tehran, Iran
[4] Univ Tehran Med Sci, Mol Immunol Res Ctr, Sch Med, Dept Immunol, Tehran, Iran
[5] Universal Sci Educ & Res Network USERN, Tehran, Iran
关键词
autoimmunity; EAMG; FOXP3; GM-CSF; myasthenia gravis; T regulatory cells; vitamin D; EXPERIMENTAL AUTOIMMUNE ENCEPHALOMYELITIS; LATE-ONSET MYASTHENIA; VITAMIN-D DEFICIENCY; GM-CSF; DENDRITIC CELLS; B-CELLS; CIRCULATING CD4(+)CD25(+); INTERLEUKIN-2; PRODUCTION; PERIPHERAL TOLERANCE; FUNCTIONAL DEFECT;
D O I
10.1586/1744666X.2015.1047345
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
T regulatory cells (Tregs) are crucial for the development of self-tolerance and are the major focus in many studies interpreting the pathogenesis of myasthenia gravis (MG), an autoimmune-based disease. In normal conditions, Tregs regulate the immune responses, while impaired regulatory function of these cells can lead to autoimmunity. Recent studies have confirmed that the thymic and peripheral blood CD4(+)CD25(+) Tregs of MG are defective in functions and/or in numbers, which are associated with disease severity; approaches to correct the defects of these Tregs may be promising in the treatment of MG. This review discusses recent studies on characteristics, quantitative and qualitative changes of Tregs and possible mechanisms that are involved in the impairment of these cells in MG pathogenesis. In addition, new approaches inducing Treg generation that are currently being investigated as therapies for MG, will be discussed as well as proposed approaches for future therapies.
引用
收藏
页码:859 / 870
页数:12
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