Human Immunological Diseases Section, Laboratory of Clinical Immunology and Microbiology, Division of Intramural Research, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Bethesda, Maryland.
Immunopathogenesis Section, Laboratory of Clinical Immunology and Microbiology, Division of Intramural Research, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Bethesda, Maryland.
Curr Protoc. 2022 Aug;2(8):e511. doi: 10.1002/cpz1.511.
Autoantibodies (autoAbs) that neutralize type 1 interferons (T1IFNs) are a major risk factor associated with developing critical COVID-19 disease and are most commonly found in individuals over age 70 and in patients with genetic or acquired thymic defects. Swift identification of autoAb-positive individuals may allow targeted interventions to prevent critical COVID-19 disease. Herein, we provide a workflow and protocols aimed at rapidly identifying individuals who are autoAb positive from a large cohort. Basic Protocol 1 describes a multiplex particle-based assay to screen large cohorts of individuals for binding levels of anti-T1IFN autoAbs, and Basic Protocol 2 describes a functional assay to test if autoAbs in patient plasma can block T1IFN-induced JAK/STAT signaling. © Published 2022. This article is a U.S. Government work and is in the public domain in the USA. Basic Protocol 1: Multiplex particle-based bead assay to screen for binding levels of anti-type 1 interferon autoantibodies Alternate Protocol: Multiplex particle-based bead assay to screen for binding levels of anti-type 1 interferon immunoglobulin subtypes and isotypes Support Protocol: Coupling type 1 interferons (IFN-α, IFN-β, and IFN-ω) to magnetic beads Basic Protocol 2: pSTAT1 functional assay to test for neutralization activity of anti-type 1 interferon autoantibodies.
自身抗体 (autoAbs) 能中和 1 型干扰素 (T1IFNs),是导致 COVID-19 重症的主要风险因素,此类自身抗体最常出现在 70 岁以上的人群和存在胸腺发育不全的遗传或获得性缺陷的患者中。快速识别自身抗体阳性个体,可能有助于针对这些个体采取干预措施,预防 COVID-19 重症的发生。本文提供了一种工作流程和方案,旨在从大样本中快速鉴定自身抗体阳性个体。基础方案 1 描述了一种基于微粒的多重检测方法,用于检测大量个体中抗 1 型干扰素自身抗体的结合水平;基础方案 2 描述了一种功能性检测方法,用于检测患者血浆中的自身抗体是否能阻断 1 型干扰素诱导的 JAK/STAT 信号通路。© 2022 年出版。本文是美国政府的作品,在美国属于公有领域。基础方案 1:基于微粒的多重检测方法,用于检测抗 1 型干扰素自身抗体的结合水平可选方案 1:基于微粒的多重检测方法,用于检测抗 1 型干扰素免疫球蛋白亚型和同种型的结合水平支持方案:将 1 型干扰素 (IFN-α、IFN-β 和 IFN-ω) 偶联到磁珠上基础方案 2:pSTAT1 功能性检测方法,用于检测抗 1 型干扰素自身抗体的中和活性