Human inborn errors of immunity underlying superficial or invasive candidiasis

被引:60
|
作者
Puel, Anne [1 ,2 ,3 ]
机构
[1] Necker Hosp Sick Children, Necker Branch, Lab Human Genet Infect Dis, INSERM,U1163, F-75015 Paris, France
[2] Paris Univ, Imagine Inst, F-75015 Paris, France
[3] Rockefeller Univ, Rockefeller Branch, St Giles Lab Human Genet Infect Dis, New York, NY 10065 USA
关键词
CHRONIC MUCOCUTANEOUS CANDIDIASIS; GAIN-OF-FUNCTION; CENTRAL-NERVOUS-SYSTEM; MUTATIONS IMPAIR IL-17; GROWTH-FACTOR-BETA; HYPER IGE SYNDROME; FUNGAL-INFECTIONS; CLINICAL-FEATURES; CARD9; DEFICIENCY; ANTIFUNGAL IMMUNITY;
D O I
10.1007/s00439-020-02141-7
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Candida species, including C. albicans in particular, can cause superficial or invasive disease, often in patients with known acquired immunodeficiencies or iatrogenic conditions. The molecular and cellular basis of these infections in patients with such risk factors remained largely elusive, until the study of inborn errors of immunity clarified the basis of the corresponding inherited and "idiopathic" infections. Superficial candidiasis, also known as chronic mucocutaneous candidiasis (CMC), can be caused by inborn errors of IL-17 immunity. Invasive candidiasis can be caused by inborn errors of CARD9 immunity. In this chapter, we review both groups of inborn errors of immunity, and discuss the contribution of these studies to the deciphering of the critical mechanisms of anti-Candida immunity in patients with other conditions.
引用
收藏
页码:1011 / 1022
页数:12
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