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人类过敏性疾病实验室诊断中基于芯片的阵列技术的发展

Evolution Toward Chip-Based Arrays in the Laboratory Diagnosis of Human Allergic Disease.

作者信息

Hamilton Robert G, Croote Derek, Lupinek Christian, Matsson Per

机构信息

Department of Medicine, Johns Hopkins University School of Medicine, Baltimore, Md.

IgGenix, Inc, South San Francisco, Calif.

出版信息

J Allergy Clin Immunol Pract. 2023 Oct;11(10):2991-2999. doi: 10.1016/j.jaip.2023.08.017. Epub 2023 Aug 18.

Abstract

Multiplex-based specific IgE antibody assays have emerged into the clinical immunology laboratory through the combined use of pure, recombinant allergenic molecules and new methods to simultaneously and accurately analyze specific IgE antibodies to hundreds of allergens. This review traces the historical development and examines outstanding questions related to the strengths and limitations of these new molecular allergen multipex technologies for the assessment of human allergic sensitization. Multiplexed technologies are poised to provide the most cost-effective and comprehensive evaluation of patients with suspected allergy as compared with the commonly used singleplex autoanalyzers. How analytically sensitive and quantitative are the multiplex technologies, down to 0.1 kU/L? Because each allergen is viewed as a unique assay, how will analytical and clinical performance be documented at the manufacturing and clinical laboratory levels to guarantee reproducibility and obtain government regulatory clearance? Will interference by naturally occurring allergen-specific IgG compromise analytical performance? Successful resolution of these and other questions covered in this review will position multiplex technologies to become the single most-effective means of screening patients for allergic sensitization, assessing IgE antibody cross-reactivity, and planning therapy directed at the patient with allergy.

摘要

基于多重检测的特异性IgE抗体检测方法,通过将纯的重组变应原分子与同时准确分析针对数百种变应原的特异性IgE抗体的新方法相结合,已进入临床免疫学实验室。本综述追溯了其历史发展,并探讨了与这些新型分子变应原多重检测技术在评估人类过敏致敏方面的优势和局限性相关的突出问题。与常用的单重自动分析仪相比,多重检测技术有望为疑似过敏患者提供最具成本效益和全面的评估。多重检测技术的分析灵敏度和定量能力如何,低至0.1 kU/L?由于每种变应原都被视为一种独特的检测方法,在生产和临床实验室层面将如何记录分析和临床性能,以确保可重复性并获得政府监管许可?天然存在的变应原特异性IgG的干扰会影响分析性能吗?成功解决本综述中涵盖的这些及其他问题,将使多重检测技术成为筛查患者过敏致敏、评估IgE抗体交叉反应性以及为过敏患者制定治疗方案的最有效手段。

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