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FLU-LISA(荧光酶联免疫吸附测定):使用抗原微阵列进行高通量抗体分析。

FLU-LISA (fluorescence-linked immunosorbent assay): high-throughput antibody profiling using antigen microarrays.

机构信息

The Shraga Segal Department of Microbiology and Immunology, Ben-Gurion University of the Negev, Beer-Sheva, Israel.

National Institute of Biotechnology in the Negev, Beer-Sheva, Israel.

出版信息

Immunol Cell Biol. 2023 Mar;101(3):231-248. doi: 10.1111/imcb.12618. Epub 2023 Jan 29.

DOI:10.1111/imcb.12618
PMID:36567516
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10275175/
Abstract

Vaccination and natural infection both elicit potent humoral responses that provide protection from subsequent infections. The immune history of an individual following such exposures is in part encoded by antibodies. While there are multiple immunoassays for measuring antibody responses, the majority of these methods measure responses to a single antigen. A commonly used method for measuring antibody responses is ELISA-a semiquantitative assay that is simple to perform in research and clinical settings. Here, we present FLU-LISA (fluorescence-linked immunosorbent assay)-a novel antigen microarray-based assay for rapid high-throughput antibody profiling. The assay can be used for profiling immunoglobulin (Ig) G, IgA and IgM responses to multiple antigens simultaneously, requiring minimal amounts of sample and antigens. Using several influenza and severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) antigen microarrays, we demonstrated the specificity and sensitivity of our novel assay and compared it with the traditional ELISA, using samples from mice, chickens and humans. We also showed that our assay can be readily used with dried blood spots, which can be collected from humans and wild birds. FLU-LISA can be readily used to profile hundreds of samples against dozens of antigens in a single day, and therefore offers an attractive alternative to the traditional ELISA.

摘要

接种疫苗和自然感染都会引发强烈的体液免疫反应,从而提供对后续感染的保护。个体在经历这些暴露后的免疫史部分由抗体所编码。虽然有多种免疫测定方法可用于测量抗体反应,但这些方法大多仅测量对单个抗原的反应。测量抗体反应的常用方法是 ELISA(酶联免疫吸附测定)——一种在研究和临床环境中易于执行的半定量测定方法。在这里,我们介绍了 FLU-LISA(荧光酶联免疫吸附测定)——一种基于抗原微阵列的新型快速高通量抗体分析方法。该测定方法可用于同时分析多种抗原的 IgG、IgA 和 IgM 反应,仅需少量样本和抗原。我们使用了几种流感和严重急性呼吸综合征冠状病毒 2(SARS-CoV-2)抗原微阵列,展示了我们新型测定方法的特异性和敏感性,并将其与传统 ELISA 进行了比较,使用了来自小鼠、鸡和人类的样本。我们还表明,我们的测定方法可以很容易地与干血斑一起使用,这些血斑可以从人类和野生鸟类中采集。FLU-LISA 可以在一天内轻松地对数百个样本进行数十种抗原的分析,因此是传统 ELISA 的一个有吸引力的替代方法。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0604/10275175/6254b1eff8ab/IMCB-101-231-g005.jpg
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