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支气管扩张症的遗传病因:原发性免疫缺陷与肺部

Genetic causes of bronchiectasis: primary immune deficiencies and the lung.

作者信息

Notarangelo Luigi D, Plebani Alessandro, Mazzolari Evelina, Soresina Annarosa, Bondioni Maria Pia

机构信息

Division of Immunology, Children's Hospital, Harvard Medical School, Boston, MA 02115, USA.

出版信息

Respiration. 2007;74(3):264-75. doi: 10.1159/000101784.

Abstract

Primary immune deficiencies (PID) comprise a heterogeneous group of genetically determined disorders that affect development and/or function of innate or adaptive immunity. Consequently, patients with PID suffer from recurrent and/or severe infections that frequently involve the lung. While the nature of the immune defect often dictates the type of pathogens that may cause lung infection, there is substantial overlap of radiological findings, so that appropriate laboratory tests are mandatory to define the nature of the immune defect and to prompt appropriate treatment. At the same time, the recent identification of a large number of PID-causing genes now allows early, even presymptomatic diagnosis, thus representing an essential tool for prevention of lung damage. This review article describes the most common forms of PID, their cellular and molecular bases, and the associated lung abnormalities, and reports on available treatment.

摘要

原发性免疫缺陷病(PID)是一组由基因决定的异质性疾病,可影响先天性或适应性免疫的发育和/或功能。因此,PID患者会反复发生和/或严重感染,肺部常受累。虽然免疫缺陷的性质通常决定了可能导致肺部感染的病原体类型,但影像学表现有很大重叠,因此必须进行适当的实验室检查以确定免疫缺陷的性质并促使进行适当治疗。同时,最近发现了大量导致PID的基因,现在可以进行早期甚至症状前诊断,从而成为预防肺损伤的重要工具。本文综述描述了PID最常见的形式、其细胞和分子基础、相关的肺部异常,并报告了可用的治疗方法。

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