Human primary immunodeficiency diseases

被引:118
作者
Fischer, Alain [1 ,2 ,3 ,4 ]
机构
[1] INSERM, U768, F-75015 Paris, France
[2] Hop Necker Enfants Malad, F-75015 Paris, France
[3] Univ Paris 05, F-75006 Paris, France
[4] Assistance Publ, Unit Immunol & Hematol Pediat, F-75015 Paris, France
关键词
D O I
10.1016/j.immuni.2007.11.012
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 [免疫学];
摘要
Primary immunodeficiency diseases (PID) provide invaluable insight into immune system, notably in vivo immune responses to microorganisms as based on the variable vulnerability to pathogens and opportunistic agents. PID are also very informative in defining key checkpoints controlling immunity to self. Despite a Mendelian inheritance of most PID, mutations of a given gene can lead to a vast array of phenotypes as a function of the type of mutations, environmental factors, the occurrence of additional somatic mutations, or regulatory factors, which add considerable but hitherto underestimated complexity. Understanding the molecular pathophysiology of PID is not only contributing to a better knowledge of the immune system but may also favor new therapeutic approaches.
引用
收藏
页码:835 / 845
页数:11
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