Systemic lupus erythematosus, regulatory T cells and pregnancy

被引:1
作者
Varghese, Stephy [1 ]
Crocker, Ian [1 ]
Bruce, Ian N. [2 ,3 ]
Tower, Clare [1 ]
机构
[1] Univ Manchester, St Marys Hosp, Maternal & Fetal Hlth Res Ctr, Manchester M13 9WL, Lancs, England
[2] Univ Manchester, Arthrit Res UK Epidemiol Unit, Sch Translat Med, Manchester Acad Hlth Sci Ctr, Manchester M13 9WL, Lancs, England
[3] Cent Manchester Univ Hosp NHS Fdn Trust, Manchester NIHR Biomed Res Ctr, Kellgren Ctr Rheumatol, Manchester, Lancs, England
基金
英国惠康基金;
关键词
immune tolerance; pregnancy; systemic lupus erythematosus; T regulatory cells; IMMUNOLOGICAL SELF-TOLERANCE; PERIPHERAL-BLOOD; TGF-BETA; SPONTANEOUS-ABORTION; IN-VITRO; FETAL REJECTION; DENDRITIC CELLS; ANTIPHOSPHOLIPID ANTIBODIES; PHENOTYPIC CHARACTERIZATION; SUPPRESSIVE FUNCTION;
D O I
10.1586/ECI.11.59
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Systemic lupus erythematosus (SLE) is the most common autoimmune disease affecting women of reproductive age and is associated with poor maternal and fetal outcomes. CD4(+) CD25(+) Treg cells are a subset of T lymphocytes with potent immunosuppressive activity that play crucial roles in controlling immunological self tolerance. Evidence suggests that they are augmented in pregnancy, especially in the first trimester, suggesting an important role in early placental development. The literature describing Treg cells in SLE is conflicting, but SLE is associated with reduced numbers and functionally defective Treg cells, which may predispose pregnant women with the disease to pregnancy complications. This article discusses the role of Treg cells in SLE and pregnancy, and how these cells may contribute to poor pregnancy outcome in SLE-affected women.
引用
收藏
页码:635 / 648
页数:14
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