Sex, age, and hospitalization drive antibody responses in a COVID-19 convalescent plasma donor population
Convalescent plasma is a leading treatment for coronavirus disease 2019 (COVID-19), but there is a paucity of data identifying its therapeutic efficacy. Among 126 potential convalescent plasma donors, the humoral immune response was evaluated using a severe acute respiratory syndrome coronavirus 2 (...
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Veröffentlicht in: | The Journal of clinical investigation 2020-11, Vol.130 (11), p.6141-6150 |
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creator | Klein, Sabra L Pekosz, Andrew Park, Han-Sol Ursin, Rebecca L Shapiro, Janna R Benner, Sarah E Littlefield, Kirsten Kumar, Swetha Naik, Harnish Mukesh Betenbaugh, Michael J Shrestha, Ruchee Wu, Annie A Hughes, Robert M Burgess, Imani Caturegli, Patricio Laeyendecker, Oliver Quinn, Thomas C Sullivan, David Shoham, Shmuel Redd, Andrew D Bloch, Evan M Casadevall, Arturo Tobian, Aaron Ar |
description | Convalescent plasma is a leading treatment for coronavirus disease 2019 (COVID-19), but there is a paucity of data identifying its therapeutic efficacy. Among 126 potential convalescent plasma donors, the humoral immune response was evaluated using a severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) virus neutralization assay with Vero-E6-TMPRSS2 cells; a commercial IgG and IgA ELISA to detect the spike (S) protein S1 domain (EUROIMMUN); IgA, IgG, and IgM indirect ELISAs to detect the full-length S protein or S receptor-binding domain (S-RBD); and an IgG avidity assay. We used multiple linear regression and predictive models to assess the correlations between antibody responses and demographic and clinical characteristics. IgG titers were greater than either IgM or IgA titers for S1, full-length S, and S-RBD in the overall population. Of the 126 plasma samples, 101 (80%) had detectable neutralizing antibody (nAb) titers. Using nAb titers as the reference, the IgG ELISAs confirmed 95%-98% of the nAb-positive samples, but 20%-32% of the nAb-negative samples were still IgG ELISA positive. Male sex, older age, and hospitalization for COVID-19 were associated with increased antibody responses across the serological assays. There was substantial heterogeneity in the antibody response among potential convalescent plasma donors, but sex, age, and hospitalization emerged as factors that can be used to identify individuals with a high likelihood of having strong antiviral antibody responses. |
doi_str_mv | 10.1172/JCI142004 |
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Among 126 potential convalescent plasma donors, the humoral immune response was evaluated using a severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) virus neutralization assay with Vero-E6-TMPRSS2 cells; a commercial IgG and IgA ELISA to detect the spike (S) protein S1 domain (EUROIMMUN); IgA, IgG, and IgM indirect ELISAs to detect the full-length S protein or S receptor-binding domain (S-RBD); and an IgG avidity assay. We used multiple linear regression and predictive models to assess the correlations between antibody responses and demographic and clinical characteristics. IgG titers were greater than either IgM or IgA titers for S1, full-length S, and S-RBD in the overall population. Of the 126 plasma samples, 101 (80%) had detectable neutralizing antibody (nAb) titers. Using nAb titers as the reference, the IgG ELISAs confirmed 95%-98% of the nAb-positive samples, but 20%-32% of the nAb-negative samples were still IgG ELISA positive. Male sex, older age, and hospitalization for COVID-19 were associated with increased antibody responses across the serological assays. There was substantial heterogeneity in the antibody response among potential convalescent plasma donors, but sex, age, and hospitalization emerged as factors that can be used to identify individuals with a high likelihood of having strong antiviral antibody responses.</description><identifier>ISSN: 0021-9738</identifier><identifier>ISSN: 1558-8238</identifier><identifier>EISSN: 1558-8238</identifier><identifier>DOI: 10.1172/JCI142004</identifier><identifier>PMID: 32764200</identifier><language>eng</language><publisher>United States: American Society for Clinical Investigation</publisher><subject>Adult ; Age ; Age Factors ; Aged ; Animals ; Antibodies ; Antibodies, Viral - blood ; Antibodies, Viral - immunology ; Antibody Formation ; Antibody response ; Antigen-antibody reactions ; Avidity ; Betacoronavirus - immunology ; Betacoronavirus - metabolism ; Biomedical research ; Blood Donors ; Care and treatment ; Chlorocebus aethiops ; Convalescence ; Convalescent plasma therapy ; Coronaviridae ; Coronavirus Infections - blood ; Coronavirus Infections - immunology ; Coronavirus Infections - therapy ; Coronaviruses ; COVID-19 ; Demographic aspects ; Development and progression ; Disease age factors ; Enzyme-linked immunosorbent assay ; Female ; Hospital patients ; Hospitalization ; Humans ; Immune response (humoral) ; Immunoglobulin A ; Immunoglobulin G ; Immunoglobulin M ; Immunologic research ; Infections ; Male ; Males ; Middle Aged ; Pandemics ; Patient outcomes ; Plasma ; Pneumonia, Viral - blood ; Pneumonia, Viral - immunology ; Pneumonia, Viral - therapy ; Prediction models ; Proteins ; Regression analysis ; SARS-CoV-2 ; Severe acute respiratory syndrome coronavirus 2 ; Sex Factors ; Vero Cells ; Viral infections</subject><ispartof>The Journal of clinical investigation, 2020-11, Vol.130 (11), p.6141-6150</ispartof><rights>COPYRIGHT 2020 American Society for Clinical Investigation</rights><rights>Copyright American Society for Clinical Investigation Nov 2020</rights><rights>2020 American Society for Clinical Investigation 2020 American Society for Clinical Investigation</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c568t-824dc0d95933c2fc6ace4fee6c0d4c8031e20d0ea464da776fc6001cbd4d5ae43</citedby><cites>FETCH-LOGICAL-c568t-824dc0d95933c2fc6ace4fee6c0d4c8031e20d0ea464da776fc6001cbd4d5ae43</cites><orcidid>0000-0001-8181-9517 ; 0000-0002-0404-1315 ; 0000-0002-9402-9167 ; 0000-0002-6019-0673 ; 0000-0002-3398-331X ; 0000-0002-0730-5224 ; 0000-0002-6429-4760 ; 0000-0003-3248-1761 ; 0000-0002-8303-4219</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC7598041/pdf/$$EPDF$$P50$$Gpubmedcentral$$H</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC7598041/$$EHTML$$P50$$Gpubmedcentral$$H</linktohtml><link.rule.ids>230,314,723,776,780,881,27901,27902,53766,53768</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/32764200$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Klein, Sabra L</creatorcontrib><creatorcontrib>Pekosz, Andrew</creatorcontrib><creatorcontrib>Park, Han-Sol</creatorcontrib><creatorcontrib>Ursin, Rebecca L</creatorcontrib><creatorcontrib>Shapiro, Janna R</creatorcontrib><creatorcontrib>Benner, Sarah E</creatorcontrib><creatorcontrib>Littlefield, Kirsten</creatorcontrib><creatorcontrib>Kumar, Swetha</creatorcontrib><creatorcontrib>Naik, Harnish Mukesh</creatorcontrib><creatorcontrib>Betenbaugh, Michael J</creatorcontrib><creatorcontrib>Shrestha, Ruchee</creatorcontrib><creatorcontrib>Wu, Annie A</creatorcontrib><creatorcontrib>Hughes, Robert M</creatorcontrib><creatorcontrib>Burgess, Imani</creatorcontrib><creatorcontrib>Caturegli, Patricio</creatorcontrib><creatorcontrib>Laeyendecker, Oliver</creatorcontrib><creatorcontrib>Quinn, Thomas C</creatorcontrib><creatorcontrib>Sullivan, David</creatorcontrib><creatorcontrib>Shoham, Shmuel</creatorcontrib><creatorcontrib>Redd, Andrew D</creatorcontrib><creatorcontrib>Bloch, Evan M</creatorcontrib><creatorcontrib>Casadevall, Arturo</creatorcontrib><creatorcontrib>Tobian, Aaron Ar</creatorcontrib><title>Sex, age, and hospitalization drive antibody responses in a COVID-19 convalescent plasma donor population</title><title>The Journal of clinical investigation</title><addtitle>J Clin Invest</addtitle><description>Convalescent plasma is a leading treatment for coronavirus disease 2019 (COVID-19), but there is a paucity of data identifying its therapeutic efficacy. Among 126 potential convalescent plasma donors, the humoral immune response was evaluated using a severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) virus neutralization assay with Vero-E6-TMPRSS2 cells; a commercial IgG and IgA ELISA to detect the spike (S) protein S1 domain (EUROIMMUN); IgA, IgG, and IgM indirect ELISAs to detect the full-length S protein or S receptor-binding domain (S-RBD); and an IgG avidity assay. We used multiple linear regression and predictive models to assess the correlations between antibody responses and demographic and clinical characteristics. IgG titers were greater than either IgM or IgA titers for S1, full-length S, and S-RBD in the overall population. Of the 126 plasma samples, 101 (80%) had detectable neutralizing antibody (nAb) titers. Using nAb titers as the reference, the IgG ELISAs confirmed 95%-98% of the nAb-positive samples, but 20%-32% of the nAb-negative samples were still IgG ELISA positive. Male sex, older age, and hospitalization for COVID-19 were associated with increased antibody responses across the serological assays. There was substantial heterogeneity in the antibody response among potential convalescent plasma donors, but sex, age, and hospitalization emerged as factors that can be used to identify individuals with a high likelihood of having strong antiviral antibody responses.</description><subject>Adult</subject><subject>Age</subject><subject>Age Factors</subject><subject>Aged</subject><subject>Animals</subject><subject>Antibodies</subject><subject>Antibodies, Viral - blood</subject><subject>Antibodies, Viral - immunology</subject><subject>Antibody Formation</subject><subject>Antibody response</subject><subject>Antigen-antibody reactions</subject><subject>Avidity</subject><subject>Betacoronavirus - immunology</subject><subject>Betacoronavirus - metabolism</subject><subject>Biomedical research</subject><subject>Blood Donors</subject><subject>Care and treatment</subject><subject>Chlorocebus aethiops</subject><subject>Convalescence</subject><subject>Convalescent plasma therapy</subject><subject>Coronaviridae</subject><subject>Coronavirus Infections - blood</subject><subject>Coronavirus Infections - immunology</subject><subject>Coronavirus Infections - therapy</subject><subject>Coronaviruses</subject><subject>COVID-19</subject><subject>Demographic aspects</subject><subject>Development and progression</subject><subject>Disease age factors</subject><subject>Enzyme-linked immunosorbent assay</subject><subject>Female</subject><subject>Hospital patients</subject><subject>Hospitalization</subject><subject>Humans</subject><subject>Immune response (humoral)</subject><subject>Immunoglobulin A</subject><subject>Immunoglobulin G</subject><subject>Immunoglobulin M</subject><subject>Immunologic research</subject><subject>Infections</subject><subject>Male</subject><subject>Males</subject><subject>Middle Aged</subject><subject>Pandemics</subject><subject>Patient outcomes</subject><subject>Plasma</subject><subject>Pneumonia, Viral - blood</subject><subject>Pneumonia, Viral - immunology</subject><subject>Pneumonia, Viral - therapy</subject><subject>Prediction models</subject><subject>Proteins</subject><subject>Regression analysis</subject><subject>SARS-CoV-2</subject><subject>Severe acute respiratory syndrome coronavirus 2</subject><subject>Sex Factors</subject><subject>Vero Cells</subject><subject>Viral 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age, and hospitalization drive antibody responses in a COVID-19 convalescent plasma donor population</title><author>Klein, Sabra L ; Pekosz, Andrew ; Park, Han-Sol ; Ursin, Rebecca L ; Shapiro, Janna R ; Benner, Sarah E ; Littlefield, Kirsten ; Kumar, Swetha ; Naik, Harnish Mukesh ; Betenbaugh, Michael J ; Shrestha, Ruchee ; Wu, Annie A ; Hughes, Robert M ; Burgess, Imani ; Caturegli, Patricio ; Laeyendecker, Oliver ; Quinn, Thomas C ; Sullivan, David ; Shoham, Shmuel ; Redd, Andrew D ; Bloch, Evan M ; Casadevall, Arturo ; Tobian, Aaron Ar</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c568t-824dc0d95933c2fc6ace4fee6c0d4c8031e20d0ea464da776fc6001cbd4d5ae43</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2020</creationdate><topic>Adult</topic><topic>Age</topic><topic>Age Factors</topic><topic>Aged</topic><topic>Animals</topic><topic>Antibodies</topic><topic>Antibodies, Viral - 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E</au><au>Littlefield, Kirsten</au><au>Kumar, Swetha</au><au>Naik, Harnish Mukesh</au><au>Betenbaugh, Michael J</au><au>Shrestha, Ruchee</au><au>Wu, Annie A</au><au>Hughes, Robert M</au><au>Burgess, Imani</au><au>Caturegli, Patricio</au><au>Laeyendecker, Oliver</au><au>Quinn, Thomas C</au><au>Sullivan, David</au><au>Shoham, Shmuel</au><au>Redd, Andrew D</au><au>Bloch, Evan M</au><au>Casadevall, Arturo</au><au>Tobian, Aaron Ar</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Sex, age, and hospitalization drive antibody responses in a COVID-19 convalescent plasma donor population</atitle><jtitle>The Journal of clinical investigation</jtitle><addtitle>J Clin Invest</addtitle><date>2020-11-02</date><risdate>2020</risdate><volume>130</volume><issue>11</issue><spage>6141</spage><epage>6150</epage><pages>6141-6150</pages><issn>0021-9738</issn><issn>1558-8238</issn><eissn>1558-8238</eissn><abstract>Convalescent plasma is a leading treatment for coronavirus disease 2019 (COVID-19), but there is a paucity of data identifying its therapeutic efficacy. Among 126 potential convalescent plasma donors, the humoral immune response was evaluated using a severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) virus neutralization assay with Vero-E6-TMPRSS2 cells; a commercial IgG and IgA ELISA to detect the spike (S) protein S1 domain (EUROIMMUN); IgA, IgG, and IgM indirect ELISAs to detect the full-length S protein or S receptor-binding domain (S-RBD); and an IgG avidity assay. We used multiple linear regression and predictive models to assess the correlations between antibody responses and demographic and clinical characteristics. IgG titers were greater than either IgM or IgA titers for S1, full-length S, and S-RBD in the overall population. Of the 126 plasma samples, 101 (80%) had detectable neutralizing antibody (nAb) titers. Using nAb titers as the reference, the IgG ELISAs confirmed 95%-98% of the nAb-positive samples, but 20%-32% of the nAb-negative samples were still IgG ELISA positive. Male sex, older age, and hospitalization for COVID-19 were associated with increased antibody responses across the serological assays. There was substantial heterogeneity in the antibody response among potential convalescent plasma donors, but sex, age, and hospitalization emerged as factors that can be used to identify individuals with a high likelihood of having strong antiviral antibody responses.</abstract><cop>United States</cop><pub>American Society for Clinical Investigation</pub><pmid>32764200</pmid><doi>10.1172/JCI142004</doi><tpages>10</tpages><orcidid>https://orcid.org/0000-0001-8181-9517</orcidid><orcidid>https://orcid.org/0000-0002-0404-1315</orcidid><orcidid>https://orcid.org/0000-0002-9402-9167</orcidid><orcidid>https://orcid.org/0000-0002-6019-0673</orcidid><orcidid>https://orcid.org/0000-0002-3398-331X</orcidid><orcidid>https://orcid.org/0000-0002-0730-5224</orcidid><orcidid>https://orcid.org/0000-0002-6429-4760</orcidid><orcidid>https://orcid.org/0000-0003-3248-1761</orcidid><orcidid>https://orcid.org/0000-0002-8303-4219</orcidid><oa>free_for_read</oa></addata></record> |
fulltext | fulltext |
identifier | ISSN: 0021-9738 |
ispartof | The Journal of clinical investigation, 2020-11, Vol.130 (11), p.6141-6150 |
issn | 0021-9738 1558-8238 1558-8238 |
language | eng |
recordid | cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_7598041 |
source | MEDLINE; Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals; PubMed Central; Alma/SFX Local Collection |
subjects | Adult Age Age Factors Aged Animals Antibodies Antibodies, Viral - blood Antibodies, Viral - immunology Antibody Formation Antibody response Antigen-antibody reactions Avidity Betacoronavirus - immunology Betacoronavirus - metabolism Biomedical research Blood Donors Care and treatment Chlorocebus aethiops Convalescence Convalescent plasma therapy Coronaviridae Coronavirus Infections - blood Coronavirus Infections - immunology Coronavirus Infections - therapy Coronaviruses COVID-19 Demographic aspects Development and progression Disease age factors Enzyme-linked immunosorbent assay Female Hospital patients Hospitalization Humans Immune response (humoral) Immunoglobulin A Immunoglobulin G Immunoglobulin M Immunologic research Infections Male Males Middle Aged Pandemics Patient outcomes Plasma Pneumonia, Viral - blood Pneumonia, Viral - immunology Pneumonia, Viral - therapy Prediction models Proteins Regression analysis SARS-CoV-2 Severe acute respiratory syndrome coronavirus 2 Sex Factors Vero Cells Viral infections |
title | Sex, age, and hospitalization drive antibody responses in a COVID-19 convalescent plasma donor population |
url | https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-02-19T23%3A19%3A49IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-gale_pubme&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Sex,%20age,%20and%20hospitalization%20drive%20antibody%20responses%20in%20a%20COVID-19%20convalescent%20plasma%20donor%20population&rft.jtitle=The%20Journal%20of%20clinical%20investigation&rft.au=Klein,%20Sabra%20L&rft.date=2020-11-02&rft.volume=130&rft.issue=11&rft.spage=6141&rft.epage=6150&rft.pages=6141-6150&rft.issn=0021-9738&rft.eissn=1558-8238&rft_id=info:doi/10.1172/JCI142004&rft_dat=%3Cgale_pubme%3EA641057649%3C/gale_pubme%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=2458778405&rft_id=info:pmid/32764200&rft_galeid=A641057649&rfr_iscdi=true |