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常见可变免疫缺陷及相关并发症。

Common Variable Immune Deficiency and Associated Complications.

机构信息

Department of Medicine, Division of Infectious Disease, Wake Forest School of Medicine, Winston Salem, NC.

Division of Allergy, Immunology and Rheumatology, University of Tennessee Health Science Center, Memphis TN.

出版信息

Chest. 2019 Sep;156(3):579-593. doi: 10.1016/j.chest.2019.05.009. Epub 2019 May 22.

Abstract

Common variable immunodeficiency disorders refer to a relatively common primary immune deficiency group of diseases that present with infectious and inflammatory complications secondary to defects in antibody production and sometimes in cellular immunity. The disorder often presents in middle age or later with recurrent sinopulmonary infections, bronchiectasis, or a plethora of noninfectious complications such as autoimmune disorders, granulomatous interstitial lung disease, GI diseases, malignancies (including lymphoma), and multisystem granulomatous disease resembling sarcoidosis. Infusion of immunoglobulin by IV or subcutaneous is the mainstay of therapy. Management of complications is often difficult as immune suppression may be necessary in these conditions and entails the use of medications and biologicals which may further increase the risk for infections. Specifically, bronchiectasis, granulomatous lymphocytic interstitial lung disease, repeated sinopulmonary infections, and malignancies are sequelae of antibody deficiency that may present to the pulmonologist. This review will provide an updated understanding of the molecular aspects, differential diagnosis, presentations, and the management of common variable immunodeficiency disorders.

摘要

常见变应性免疫缺陷病是一组相对常见的原发性免疫缺陷病,其特征是由于抗体产生和(或)细胞免疫缺陷导致感染和炎症并发症。该疾病常发生于中年或中老年,表现为反复发作的鼻窦和肺部感染、支气管扩张,或出现多种非感染性并发症,如自身免疫性疾病、肉芽肿性间质性肺病、胃肠道疾病、恶性肿瘤(包括淋巴瘤)和类似于结节病的多系统肉芽肿性疾病。静脉输注或皮下注射免疫球蛋白是主要的治疗方法。由于这些情况下可能需要免疫抑制,并且需要使用药物和生物制剂,这可能会进一步增加感染的风险,因此并发症的管理往往较为困难。具体来说,支气管扩张、肉芽肿性淋巴细胞间质性肺病、反复鼻窦和肺部感染以及恶性肿瘤是抗体缺陷的后遗症,可能会由肺病专家进行诊治。本文将提供对常见变应性免疫缺陷病的分子特征、鉴别诊断、临床表现和管理的最新认识。

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