New primary immunodeficiency with infectious disease genetic predisposition

被引:0
|
作者
Picard, C
Casanova, JL
机构
[1] Hop Necker Enfants Malad, AP HP, Unite Immunol Hematol Pediat, F-75015 Paris, France
[2] Univ Paris 05, Fac Med Necker, INSERM, Lab Genet Humaine Maladies Infect,U550, F-75015 Paris, France
来源
ARCHIVES DE PEDIATRIE | 2003年 / 10卷
关键词
immunologic deficiency syndrome; mycobacterial infection; immunology; viral infections; susceptibility; genetics;
D O I
10.1016/S0929-693X(03)90059-5
中图分类号
R72 [儿科学];
学科分类号
100202 ;
摘要
Since 10 years severe pediatric infections which were idiopathic have now molecular explanation, because new primary immunodeficiencies responsible of these severe infections were identified. These children presented a new kind of hereditary immunodeficiency with severe and/or recurrent infections caused by only one microorganisms family, in opposition to other patients with "classic" primary immunodeficiency. Standard immunologic explorations for example white blood counts, lymphocyte counts, vaccine serology, immunoglobulin levels and complement were normal. However, these children presented a vulnerability, sometimes lethal, caused by one type of microorganism. The aim of this review is to describe 3 new syndromes with a genetic predisposition of infectious diseases: IL-12-IFNgamma axis deficiency (Mendelian susceptibility to mycobacterial disease), STAT1 deficiency (predisposition to viral disease) and NEMO and IRAK-4 deficiencies (predisposition to infections caused by pyogenic bacteria). (C) 2003 Elsevier SAS. All rights reserved.
引用
收藏
页码:513S / 516S
页数:4
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