Autoimmunity in common variable immunodeficiency

被引:124
作者
Agarwal, Shradha [1 ]
Cunningham-Rundles, Charlotte [1 ]
机构
[1] Mt Sinai Med Ctr, New York, NY 10029 USA
基金
美国国家卫生研究院;
关键词
MEMORY B-CELLS; SYSTEMIC-LUPUS-ERYTHEMATOSUS; SELECTIVE IGA DEFICIENCY; ANTIBODY-DEFICIENCY; GRANULOMATOUS-DISEASE; IMMUNE-DEFICIENCY; MUTATIONS; TACI; DIFFERENTIATION; CLASSIFICATION;
D O I
10.1007/s11882-009-0051-0
中图分类号
R392 [医学免疫学];
学科分类号
100102 ;
摘要
Common variable immunodeficiency (CVID) is the most common clinically significant primary immune defect. Although the hallmark of CVID is hypogammaglobulinemia, the intrinsic dysregulation of the immune system leads to defective T-cell activation and proliferation, as well as dendritic cell and cytokine defects. Although 70% to 80% of patients have had recurrent sinopulmonary infections, autoimmunity and inflammatory complications are also common. The most common autoimmune conditions are immune thrombocytopenic purpura and hemolytic anemia, but other autoimmune complications arise, including rheumatoid arthritis, pernicious anemia, primary biliary cirrhosis, thyroiditis, sicca syndrome, systemic lupus, and inflammatory bowel disease. Treatment of autoimmunity includes highdose immunoglobulins, corticosteroids, selected immu no suppressants, and other immune modulators. This review focuses on autoimmune conditions associated with CVID, potential mechanisms of immune dysregulation, and therapeutic strategies.
引用
收藏
页码:347 / 352
页数:6
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