原发性免疫缺陷病的诊断测试:经典检测和基因检测。

Natchanun Klangkalya,Thomas A Fleisher,Sergio D Rosenzweig
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引用次数: 0

摘要

原发性免疫缺陷病包括多种遗传病,其特点是免疫系统受损,通常会导致感染易感性增加。事实上,它们还表现为自身免疫、自身炎症、特应性疾病和恶性肿瘤。目前,公认的单基因原发性免疫缺陷病的数量已达到 500 种以上,这主要归功于在发现疾病时大量使用无偏见的基因检测。此外,由于越来越多地使用免疫抑制剂来治疗基于免疫失调的疾病、接受造血干细胞移植的人数增加以及包括自身免疫在内的其他慢性疾病,继发性免疫缺陷的发病率也在不断上升。虽然免疫缺陷疾病的临床症状很广泛,但早期诊断和有针对性的管理策略对于降低感染风险和预防疾病相关发病率至关重要。一般来说,病史和体格检查可以提供有用的信息,帮助确定免疫缺陷的可能性。反过来,这样就可以根据受影响的特定免疫细胞及其功能或产物,选择有针对性的实验室检测来确定免疫缺陷疾病。实验室评估包括定量和功能性经典检测(如白细胞计数、血清免疫球蛋白水平、对疫苗反应的特异性抗体滴度和淋巴细胞亚群计数)以及基因检测(如通过桑格测序进行的单个基因评估或基于新一代测序的无偏见评估)。然而,在许多情况下,诊断还需要额外的先进研究技术来验证基因或其他发现。本文向临床医生介绍了评估原发性免疫缺陷疾病患者免疫系统的可用实验室检测方法。它还根据宿主防御的不同组成部分提供了一份全面的检测选项清单。
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Diagnostic tests for primary immunodeficiency disorders: Classic and genetic testing.
Primary immunodeficiency diseases encompass a variety of genetic conditions characterized by a compromised immune system and typically results in increased susceptibility to infection. In fact, they also manifest as autoimmunity, autoinflammation, atopic diseases, and malignancy. Currently, the number of recognized monogenic primary immunodeficiency disorders is set at ∼500 different entities, owing to the exponential use of unbiased genetic testing for disease discovery. In addition, the prevalence of secondary immunodeficiency has also been on the rise due to the increased use of immunosuppressive drugs to treat diseases based on immune dysregulation, an increase in the number of individuals undergoing hematopoietic stem cell transplantation, and other chronic medical conditions, including autoimmunity. Although the clinical symptoms of immunodeficiency disorders are broad, an early diagnosis and tailored management strategies are essential to mitigate the risk of infections and prevent disease-associated morbidity. Generally, the medical history and physical examination can provide useful information that can help delineate the possibility of immune defects. In turn, this makes it feasible to select focused laboratory tests that identify immunodeficiency disorders based on the specific immune cells and their functions or products that are affected. Laboratory evaluation involves quantitative and functional classic testing (e.g., leukocyte counts, serum immunoglobulin levels, specific antibody titers in response to vaccines, and enumeration of lymphocyte subsets) as well as genetic testing (e.g., individual gene evaluation via Sanger sequencing or unbiased evaluation based on next-generation sequencing). However, in many cases, a diagnosis also requires additional advanced research techniques to validate genetic or other findings. This article updates clinicians about available laboratory tests for evaluating the immune system in patients with primary immunodeficiency disorders. It also provides a comprehensive list of testing options, organized based on different components of host defense.
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Real-world outcomes in patients with hereditary angioedema prescribed lanadelumab versus other prophylaxis. Protective antibody concentrations in primary immunodeficiency following infusion with 5% or 10% intravenous immunoglobulin. Immunodeficiency: Overview of primary immune regulatory disorders (PIRDs). Essentials of an immunodeficiency primer: A practical reference for the allergist/immunologist and the allergy-immunology fellow-in-training (FIT). Immunodeficiency: Gene therapy for primary immune deficiency.
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