Primary immune deficiency disorders presenting as autoimmune diseases: IPEX and APECED

被引:73
作者
Moraes-Vasconcelos, D. [1 ,2 ]
Costa-Carvalho, B. T. [3 ]
Torgerson, T. R. [4 ,5 ]
Ochs, H. D. [4 ,5 ]
机构
[1] Univ Sao Paulo, Sch Med, Lab Med Investigat Dermatol & Immunodeficiencies, Sao Paulo, Brazil
[2] Univ Sao Paulo, Sch Med, Primary Immunodeficiency Outpatient Unit ADEE 300, Sao Paulo, Brazil
[3] Univ Fed Sao Paulo, Div Allergy Clin Immunol & Rheumatol, Dept Pediat, Escola Paulista Med, Sao Paulo, Brazil
[4] Univ Washington, Sch Med, Dept Pediat, Seattle, WA 98195 USA
[5] Childrens Hosp, Regional Med Ctr, Seattle, WA USA
关键词
autoinimunity; autoimmune regulator (AIRE); autoininume polyendocrinopathy; candidiasis and ectodermal dystrophy (APECED); forkhead box P3 (FOXP3); immune tolerance; immune dysregulation; polyendocrinopathy; enteropathy and X-linked (IPEX); primary immune deficiency disorders (PIDD);
D O I
10.1007/s10875-008-9176-5
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Background Several primary immune deficiency disorders are associated with autoimmunity and malignancy, suggesting a state of immune dysregulation. The concept of immune dysregulation as a direct cause of autoimmunity in primary immune deficiency disorders (PIDDs) has been strengthened by the recent discovery of distinct clinical entities linked to single-gene defects resulting in multiple autoimmune phenomena including immune dysregulation, polyendocrinopathy, enteropathy and X-linked (IPEX) syndrome, and autoimmune polyendocrinopathy, candidiasis and ectodermal dystrophy (APECED) syndrome. Conclusion Reviewing recent advances in our understanding of the small subgroup of PIDD patients with defined causes for autoimmunity may lead to the development of more effective treatment strategies for idiopathic human autoimmune diseases.
引用
收藏
页码:S11 / S19
页数:9
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