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X连锁免疫缺陷病的分子基础。

The molecular basis of X-linked immunodeficiency disease.

作者信息

Kinnon C, Levinsky R

机构信息

Molecular Immunology Unit, University of London, UK.

出版信息

J Inherit Metab Dis. 1992;15(4):674-82. doi: 10.1007/BF01799623.

Abstract

The molecular bases of the X-linked immunodeficiency diseases remain largely undetermined. Two of the genes involved in these diseases have been isolated, namely the genes for X-linked chronic granulomatous disease and properdin deficiency, and substantial progress has now been made in identifying the genes which are defective in the other five diseases, Wiskott-Aldrich syndrome, X-linked severe combined immunodeficiency, X-linked agammaglobulinaemia, X-linked hyper-IgM and X-linked lymphoproliferative syndrome. We review here the nature of the diseases, progress made in identifying and isolating the genes involved and the prospects for improved prenatal detection, carrier status determination and treatment of these life-threatening conditions.

摘要

X连锁免疫缺陷疾病的分子基础在很大程度上仍未明确。已分离出与这些疾病相关的两个基因,即X连锁慢性肉芽肿病基因和备解素缺乏症基因,并且在确定其他五种疾病(威斯科特-奥尔德里奇综合征、X连锁严重联合免疫缺陷、X连锁无丙种球蛋白血症、X连锁高IgM血症和X连锁淋巴增殖综合征)中存在缺陷的基因方面现已取得了实质性进展。我们在此综述这些疾病的本质、在鉴定和分离相关基因方面取得的进展,以及改善这些危及生命疾病的产前检测、携带者状态判定和治疗的前景。

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