成年期先天性免疫错误

Joanne J. F. Wang, Arün Dhir, Kyla J. Hildebrand, Stuart E. Turvey, Robert Schellenberg, Luke Y. C. Chen, Persia Pourshahnazari, Catherine M. Biggs
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引用次数: 0

摘要

先天性免疫错误(IEIs)是一组免疫系统部分缺失或功能障碍的疾病。人们一度认为它主要是一种儿科疾病,但现在估计全球 50%以上的先天性免疫错误病例是由成年人引起的。延迟诊断、晚期症状发作和 IEI 表型复制都可能导致成人发病的 IEI。对成人 IEI 表现的多样性缺乏认识也是导致诊断和治疗延误的原因之一。及时转诊到免疫科至关重要,这样患者才能得到精确的分子诊断,并在有条件时接受针对性治疗。本文作为成人 IEI 的入门读物,重点介绍了病理生理学、流行病学和临床特征。我们介绍了三种主要 IEI 的临床病例,以帮助临床医生根据病例建立疾病脚本。我们为实验室评估 IEI 及其初始治疗提供了一个框架,目的是提高对这些病症的识别和管理。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Inborn errors of immunity in adulthood
Inborn errors of immunity (IEIs) are a group of conditions whereby parts of the immune system are missing or dysfunctional. Once thought to primarily be a pediatric disorder, it is now estimated that more than 50% of worldwide incident IEI cases are accounted for by adults. Delayed diagnosis, late symptom onset, and IEI phenocopies can all lead to adult-onset recognition of IEIs. Lack of awareness regarding the diversity of IEI manifestations in adults contributes to diagnostic and treatment delays. Prompt referral to immunology is critical so that patients can receive a precise molecular diagnosis and targeted therapy when available. This article serves as a primer on IEIs in adulthood, highlighting the pathophysiology, epidemiology and clinical features. We present clinical vignettes of three key IEIs to assist clinicians in building illness scripts on their presentations. We provide a framework for the laboratory evaluation of IEIs and their initial treatment, with the aim of improving recognition and management of these conditions.
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