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

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 majori...

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Autores principales: Levy, Shlomia, Abd Alhadi, Marwa, Azulay, Asaf, Kahana, Amit, Bujanover, Nir, Gazit, Roi, McGargill, Maureen A, Friedman, Lilach M, Hertz, Tomer
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10275175/
https://www.ncbi.nlm.nih.gov/pubmed/36567516
http://dx.doi.org/10.1111/imcb.12618
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author Levy, Shlomia
Abd Alhadi, Marwa
Azulay, Asaf
Kahana, Amit
Bujanover, Nir
Gazit, Roi
McGargill, Maureen A
Friedman, Lilach M
Hertz, Tomer
author_facet Levy, Shlomia
Abd Alhadi, Marwa
Azulay, Asaf
Kahana, Amit
Bujanover, Nir
Gazit, Roi
McGargill, Maureen A
Friedman, Lilach M
Hertz, Tomer
author_sort Levy, Shlomia
collection PubMed
description 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.
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spelling pubmed-102751752023-06-17 FLU‐LISA (fluorescence‐linked immunosorbent assay): high‐throughput antibody profiling using antigen microarrays Levy, Shlomia Abd Alhadi, Marwa Azulay, Asaf Kahana, Amit Bujanover, Nir Gazit, Roi McGargill, Maureen A Friedman, Lilach M Hertz, Tomer Immunol Cell Biol Original Articles 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. John Wiley and Sons Inc. 2023-01-29 2023-03 /pmc/articles/PMC10275175/ /pubmed/36567516 http://dx.doi.org/10.1111/imcb.12618 Text en © 2022 The Authors. Immunology & Cell Biology published by John Wiley & Sons Australia, Ltd on behalf of the Australian and New Zealand Society for Immunology, Inc. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ (https://creativecommons.org/licenses/by-nc-nd/4.0/) License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made.
spellingShingle Original Articles
Levy, Shlomia
Abd Alhadi, Marwa
Azulay, Asaf
Kahana, Amit
Bujanover, Nir
Gazit, Roi
McGargill, Maureen A
Friedman, Lilach M
Hertz, Tomer
FLU‐LISA (fluorescence‐linked immunosorbent assay): high‐throughput antibody profiling using antigen microarrays
title FLU‐LISA (fluorescence‐linked immunosorbent assay): high‐throughput antibody profiling using antigen microarrays
title_full FLU‐LISA (fluorescence‐linked immunosorbent assay): high‐throughput antibody profiling using antigen microarrays
title_fullStr FLU‐LISA (fluorescence‐linked immunosorbent assay): high‐throughput antibody profiling using antigen microarrays
title_full_unstemmed FLU‐LISA (fluorescence‐linked immunosorbent assay): high‐throughput antibody profiling using antigen microarrays
title_short FLU‐LISA (fluorescence‐linked immunosorbent assay): high‐throughput antibody profiling using antigen microarrays
title_sort flu‐lisa (fluorescence‐linked immunosorbent assay): high‐throughput antibody profiling using antigen microarrays
topic Original Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10275175/
https://www.ncbi.nlm.nih.gov/pubmed/36567516
http://dx.doi.org/10.1111/imcb.12618
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