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...
Gespeichert in:
Veröffentlicht in: | Immunology and cell biology 2023-03, Vol.101 (3), p.231-248 |
---|---|
Hauptverfasser: | , , , , , , , , |
Format: | Artikel |
Sprache: | eng |
Schlagworte: | |
Online-Zugang: | Volltext |
Tags: |
Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
|
container_end_page | 248 |
---|---|
container_issue | 3 |
container_start_page | 231 |
container_title | Immunology and cell biology |
container_volume | 101 |
creator | Levy, Shlomia Abd Alhadi, Marwa Azulay, Asaf Kahana, Amit Bujanover, Nir Gazit, Roi McGargill, Maureen A Friedman, Lilach M Hertz, Tomer |
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.
We developed a novel high‐throughput antibody binding assay for profiling immune history to previous infections and vaccines. We demonstrate its use using samples from mice, birds and humans, and compare it with the traditional ELISA. |
doi_str_mv | 10.1111/imcb.12618 |
format | Article |
fullrecord | <record><control><sourceid>proquest_pubme</sourceid><recordid>TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_10275175</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>2780637908</sourcerecordid><originalsourceid>FETCH-LOGICAL-c4498-88a22ee8c0c4140b0bb4604c83ecb363705e30a1f6c845063283b00681c3438f3</originalsourceid><addsrcrecordid>eNp9kcFu1DAQhi0EotvChQdAkbgUpBQ7dhwvF1RWFFZaxAF6tmyvk7gk9mLHRbn1EXhGnoRZtlTAAR9saebzr5n_R-gJwWcEzks3Gn1GKk7EPbQgjOGSNITcRwssiCiXnJEjdJzSFca4qQR9iI4or3lTE75A1xebyx833zfrT-fFaTvkEG0y1hsLxcH5L3ZbuHHMPqQQtfVToVJS8_NXRe-6HpipjyF3_S5Dx09Oh-1c7GJoHXzuipz2977RWV-MzsSgYlRzeoQetGpI9vHte4IuL95-Xr0vNx_frVfnm9IwthSlEKqqrBUGG0YY1lhrxjEzglqjKacNri3FirTcCFZjTmE9jTEXxFBGRUtP0OuD7i7r0W5hsymqQe6iG1WcZVBO_t3xrpdduJYEV2BQU4PC6a1CDF-zTZMcHTg0DMrbkJMETNCaiWYJ6LN_0KuQo4f9gBIwXbPEAqgXBwrMSCna9m4aguU-T7nPU_7KE-Cnf85_h_4OEAByAL65wc7_kZLrD6s3B9Gf7tivLg</addsrcrecordid><sourcetype>Open Access Repository</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>2780637908</pqid></control><display><type>article</type><title>FLU‐LISA (fluorescence‐linked immunosorbent assay): high‐throughput antibody profiling using antigen microarrays</title><source>MEDLINE</source><source>Wiley Online Library Journals Frontfile Complete</source><creator>Levy, Shlomia ; Abd Alhadi, Marwa ; Azulay, Asaf ; Kahana, Amit ; Bujanover, Nir ; Gazit, Roi ; McGargill, Maureen A ; Friedman, Lilach M ; Hertz, Tomer</creator><creatorcontrib>Levy, Shlomia ; Abd Alhadi, Marwa ; Azulay, Asaf ; Kahana, Amit ; Bujanover, Nir ; Gazit, Roi ; McGargill, Maureen A ; Friedman, Lilach M ; Hertz, Tomer</creatorcontrib><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.
We developed a novel high‐throughput antibody binding assay for profiling immune history to previous infections and vaccines. We demonstrate its use using samples from mice, birds and humans, and compare it with the traditional ELISA.</description><identifier>ISSN: 0818-9641</identifier><identifier>EISSN: 1440-1711</identifier><identifier>DOI: 10.1111/imcb.12618</identifier><identifier>PMID: 36567516</identifier><language>eng</language><publisher>United States: Blackwell Science Ltd</publisher><subject>Animals ; Antibodies ; Antibodies, Viral ; Antibody profiling ; antigen microarrays ; Antigens ; Chickens ; Coronaviruses ; COVID-19 ; ELISA ; Enzyme-Linked Immunosorbent Assay ; FLU‐LISA ; Humans ; immune history ; Immunoglobulin A ; Immunoglobulin G ; Immunoglobulin M ; Immunosorbents ; Influenza ; Influenza, Human ; Mice ; Original ; SARS-CoV-2 ; Severe acute respiratory syndrome coronavirus 2 ; Vaccination</subject><ispartof>Immunology and cell biology, 2023-03, Vol.101 (3), p.231-248</ispartof><rights>2022 The Authors. published by John Wiley & Sons Australia, Ltd on behalf of the Australian and New Zealand Society for Immunology, Inc.</rights><rights>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.</rights><rights>2022. This article is published under http://creativecommons.org/licenses/by-nc-nd/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c4498-88a22ee8c0c4140b0bb4604c83ecb363705e30a1f6c845063283b00681c3438f3</citedby><cites>FETCH-LOGICAL-c4498-88a22ee8c0c4140b0bb4604c83ecb363705e30a1f6c845063283b00681c3438f3</cites><orcidid>0000-0002-0561-1578 ; 0000-0002-0916-0372</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1111%2Fimcb.12618$$EPDF$$P50$$Gwiley$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1111%2Fimcb.12618$$EHTML$$P50$$Gwiley$$Hfree_for_read</linktohtml><link.rule.ids>230,314,776,780,881,1411,27903,27904,45553,45554</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/36567516$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Levy, Shlomia</creatorcontrib><creatorcontrib>Abd Alhadi, Marwa</creatorcontrib><creatorcontrib>Azulay, Asaf</creatorcontrib><creatorcontrib>Kahana, Amit</creatorcontrib><creatorcontrib>Bujanover, Nir</creatorcontrib><creatorcontrib>Gazit, Roi</creatorcontrib><creatorcontrib>McGargill, Maureen A</creatorcontrib><creatorcontrib>Friedman, Lilach M</creatorcontrib><creatorcontrib>Hertz, Tomer</creatorcontrib><title>FLU‐LISA (fluorescence‐linked immunosorbent assay): high‐throughput antibody profiling using antigen microarrays</title><title>Immunology and cell biology</title><addtitle>Immunol Cell Biol</addtitle><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.
We developed a novel high‐throughput antibody binding assay for profiling immune history to previous infections and vaccines. We demonstrate its use using samples from mice, birds and humans, and compare it with the traditional ELISA.</description><subject>Animals</subject><subject>Antibodies</subject><subject>Antibodies, Viral</subject><subject>Antibody profiling</subject><subject>antigen microarrays</subject><subject>Antigens</subject><subject>Chickens</subject><subject>Coronaviruses</subject><subject>COVID-19</subject><subject>ELISA</subject><subject>Enzyme-Linked Immunosorbent Assay</subject><subject>FLU‐LISA</subject><subject>Humans</subject><subject>immune history</subject><subject>Immunoglobulin A</subject><subject>Immunoglobulin G</subject><subject>Immunoglobulin M</subject><subject>Immunosorbents</subject><subject>Influenza</subject><subject>Influenza, Human</subject><subject>Mice</subject><subject>Original</subject><subject>SARS-CoV-2</subject><subject>Severe acute respiratory syndrome coronavirus 2</subject><subject>Vaccination</subject><issn>0818-9641</issn><issn>1440-1711</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2023</creationdate><recordtype>article</recordtype><sourceid>24P</sourceid><sourceid>EIF</sourceid><recordid>eNp9kcFu1DAQhi0EotvChQdAkbgUpBQ7dhwvF1RWFFZaxAF6tmyvk7gk9mLHRbn1EXhGnoRZtlTAAR9saebzr5n_R-gJwWcEzks3Gn1GKk7EPbQgjOGSNITcRwssiCiXnJEjdJzSFca4qQR9iI4or3lTE75A1xebyx833zfrT-fFaTvkEG0y1hsLxcH5L3ZbuHHMPqQQtfVToVJS8_NXRe-6HpipjyF3_S5Dx09Oh-1c7GJoHXzuipz2977RWV-MzsSgYlRzeoQetGpI9vHte4IuL95-Xr0vNx_frVfnm9IwthSlEKqqrBUGG0YY1lhrxjEzglqjKacNri3FirTcCFZjTmE9jTEXxFBGRUtP0OuD7i7r0W5hsymqQe6iG1WcZVBO_t3xrpdduJYEV2BQU4PC6a1CDF-zTZMcHTg0DMrbkJMETNCaiWYJ6LN_0KuQo4f9gBIwXbPEAqgXBwrMSCna9m4aguU-T7nPU_7KE-Cnf85_h_4OEAByAL65wc7_kZLrD6s3B9Gf7tivLg</recordid><startdate>202303</startdate><enddate>202303</enddate><creator>Levy, Shlomia</creator><creator>Abd Alhadi, Marwa</creator><creator>Azulay, Asaf</creator><creator>Kahana, Amit</creator><creator>Bujanover, Nir</creator><creator>Gazit, Roi</creator><creator>McGargill, Maureen A</creator><creator>Friedman, Lilach M</creator><creator>Hertz, Tomer</creator><general>Blackwell Science Ltd</general><general>John Wiley and Sons Inc</general><scope>24P</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>K9.</scope><scope>7X8</scope><scope>5PM</scope><orcidid>https://orcid.org/0000-0002-0561-1578</orcidid><orcidid>https://orcid.org/0000-0002-0916-0372</orcidid></search><sort><creationdate>202303</creationdate><title>FLU‐LISA (fluorescence‐linked immunosorbent assay): high‐throughput antibody profiling using antigen microarrays</title><author>Levy, Shlomia ; Abd Alhadi, Marwa ; Azulay, Asaf ; Kahana, Amit ; Bujanover, Nir ; Gazit, Roi ; McGargill, Maureen A ; Friedman, Lilach M ; Hertz, Tomer</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4498-88a22ee8c0c4140b0bb4604c83ecb363705e30a1f6c845063283b00681c3438f3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2023</creationdate><topic>Animals</topic><topic>Antibodies</topic><topic>Antibodies, Viral</topic><topic>Antibody profiling</topic><topic>antigen microarrays</topic><topic>Antigens</topic><topic>Chickens</topic><topic>Coronaviruses</topic><topic>COVID-19</topic><topic>ELISA</topic><topic>Enzyme-Linked Immunosorbent Assay</topic><topic>FLU‐LISA</topic><topic>Humans</topic><topic>immune history</topic><topic>Immunoglobulin A</topic><topic>Immunoglobulin G</topic><topic>Immunoglobulin M</topic><topic>Immunosorbents</topic><topic>Influenza</topic><topic>Influenza, Human</topic><topic>Mice</topic><topic>Original</topic><topic>SARS-CoV-2</topic><topic>Severe acute respiratory syndrome coronavirus 2</topic><topic>Vaccination</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Levy, Shlomia</creatorcontrib><creatorcontrib>Abd Alhadi, Marwa</creatorcontrib><creatorcontrib>Azulay, Asaf</creatorcontrib><creatorcontrib>Kahana, Amit</creatorcontrib><creatorcontrib>Bujanover, Nir</creatorcontrib><creatorcontrib>Gazit, Roi</creatorcontrib><creatorcontrib>McGargill, Maureen A</creatorcontrib><creatorcontrib>Friedman, Lilach M</creatorcontrib><creatorcontrib>Hertz, Tomer</creatorcontrib><collection>Wiley Online Library Open Access</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Immunology and cell biology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Levy, Shlomia</au><au>Abd Alhadi, Marwa</au><au>Azulay, Asaf</au><au>Kahana, Amit</au><au>Bujanover, Nir</au><au>Gazit, Roi</au><au>McGargill, Maureen A</au><au>Friedman, Lilach M</au><au>Hertz, Tomer</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>FLU‐LISA (fluorescence‐linked immunosorbent assay): high‐throughput antibody profiling using antigen microarrays</atitle><jtitle>Immunology and cell biology</jtitle><addtitle>Immunol Cell Biol</addtitle><date>2023-03</date><risdate>2023</risdate><volume>101</volume><issue>3</issue><spage>231</spage><epage>248</epage><pages>231-248</pages><issn>0818-9641</issn><eissn>1440-1711</eissn><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.
We developed a novel high‐throughput antibody binding assay for profiling immune history to previous infections and vaccines. We demonstrate its use using samples from mice, birds and humans, and compare it with the traditional ELISA.</abstract><cop>United States</cop><pub>Blackwell Science Ltd</pub><pmid>36567516</pmid><doi>10.1111/imcb.12618</doi><tpages>248</tpages><orcidid>https://orcid.org/0000-0002-0561-1578</orcidid><orcidid>https://orcid.org/0000-0002-0916-0372</orcidid><oa>free_for_read</oa></addata></record> |
fulltext | fulltext |
identifier | ISSN: 0818-9641 |
ispartof | Immunology and cell biology, 2023-03, Vol.101 (3), p.231-248 |
issn | 0818-9641 1440-1711 |
language | eng |
recordid | cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_10275175 |
source | MEDLINE; Wiley Online Library Journals Frontfile Complete |
subjects | Animals Antibodies Antibodies, Viral Antibody profiling antigen microarrays Antigens Chickens Coronaviruses COVID-19 ELISA Enzyme-Linked Immunosorbent Assay FLU‐LISA Humans immune history Immunoglobulin A Immunoglobulin G Immunoglobulin M Immunosorbents Influenza Influenza, Human Mice Original SARS-CoV-2 Severe acute respiratory syndrome coronavirus 2 Vaccination |
title | FLU‐LISA (fluorescence‐linked immunosorbent assay): high‐throughput antibody profiling using antigen microarrays |
url | https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-25T01%3A02%3A46IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_pubme&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=FLU%E2%80%90LISA%20(fluorescence%E2%80%90linked%20immunosorbent%20assay):%20high%E2%80%90throughput%20antibody%20profiling%20using%20antigen%20microarrays&rft.jtitle=Immunology%20and%20cell%20biology&rft.au=Levy,%20Shlomia&rft.date=2023-03&rft.volume=101&rft.issue=3&rft.spage=231&rft.epage=248&rft.pages=231-248&rft.issn=0818-9641&rft.eissn=1440-1711&rft_id=info:doi/10.1111/imcb.12618&rft_dat=%3Cproquest_pubme%3E2780637908%3C/proquest_pubme%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=2780637908&rft_id=info:pmid/36567516&rfr_iscdi=true |