ABO blood group is involved in the quality of the specific immune response anti-SARS-CoV-2
Since December 2019, the coronavirus disease 2019 (COVID-19), caused by the severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2), has spread throughout the world. To eradicate it, it is crucial to acquire a strong and long-lasting anti-SARS-CoV-2 immunity, by either natural infection or vacc...
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creator | Gil-Manso, Sergio Miguens Blanco, Iria Motyka, Bruce Halpin, Anne López-Esteban, Rocío Pérez-Fernández, Verónica Astrid Carbonell, Diego López-Fernández, Luis Andrés West, Lori Correa-Rocha, Rafael Pion, Marjorie |
description | Since December 2019, the coronavirus disease 2019 (COVID-19), caused by the severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2), has spread throughout the world. To eradicate it, it is crucial to acquire a strong and long-lasting anti-SARS-CoV-2 immunity, by either natural infection or vaccination. We collected blood samples 12-305 days after positive polymerase chain reactions (PCRs) from 35 recovered individuals infected by SARS-CoV-2. Peripheral blood mononuclear cells were stimulated with SARS-CoV-2-derived peptide pools, such as the spike (S), nucleocapsid (N) and membrane (M) proteins, and we quantified anti-S immunoglobulins in plasma. After 10 months post-infection, we observed a sustained SARS-CoV-2-specific CD4+ T-cell response directed against M-protein, but responses against S- or N-proteins were lost over time. Besides, we demonstrated that O-group individuals presented significantly lower frequencies of specific CD4+ T-cell responses against Pep-M than non O-group individuals. The non O-group subjects also needed longer to clear the virus, and they lost cellular immune responses over time, compared to the O-group individuals, who showed a persistent specific immune response against SARS-CoV-2. Therefore, the S-specific immune response was lost over time, and individual factors might determine the sustainability of the body's defenses, which must be considered in the future design of vaccines to achieve continuous anti-SARS-CoV-2 immunity. |
doi_str_mv | 10.1080/21505594.2021.2019959 |
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To eradicate it, it is crucial to acquire a strong and long-lasting anti-SARS-CoV-2 immunity, by either natural infection or vaccination. We collected blood samples 12-305 days after positive polymerase chain reactions (PCRs) from 35 recovered individuals infected by SARS-CoV-2. Peripheral blood mononuclear cells were stimulated with SARS-CoV-2-derived peptide pools, such as the spike (S), nucleocapsid (N) and membrane (M) proteins, and we quantified anti-S immunoglobulins in plasma. After 10 months post-infection, we observed a sustained SARS-CoV-2-specific CD4+ T-cell response directed against M-protein, but responses against S- or N-proteins were lost over time. Besides, we demonstrated that O-group individuals presented significantly lower frequencies of specific CD4+ T-cell responses against Pep-M than non O-group individuals. The non O-group subjects also needed longer to clear the virus, and they lost cellular immune responses over time, compared to the O-group individuals, who showed a persistent specific immune response against SARS-CoV-2. Therefore, the S-specific immune response was lost over time, and individual factors might determine the sustainability of the body's defenses, which must be considered in the future design of vaccines to achieve continuous anti-SARS-CoV-2 immunity.</description><identifier>ISSN: 2150-5594</identifier><identifier>ISSN: 2150-5608</identifier><identifier>EISSN: 2150-5608</identifier><identifier>DOI: 10.1080/21505594.2021.2019959</identifier><identifier>PMID: 34967260</identifier><language>eng</language><publisher>United States: Taylor & Francis</publisher><subject>ABO Blood-Group System ; ABO group ; COVID-19 - blood ; Humans ; humoral immune response ; Immunity, Cellular ; Immunity, Humoral ; individual factors ; Leukocytes, Mononuclear ; Memory T Cells ; memory T-cell response ; Research Paper ; SARS-CoV-2 ; SARS-CoV-2 - immunology ; Spike Glycoprotein, Coronavirus</subject><ispartof>Virulence, 2022-12, Vol.13 (1), p.30-45</ispartof><rights>2021 The Author(s). Published by Informa UK Limited, trading as Taylor & Francis Group. 2021</rights><rights>2021 The Author(s). 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To eradicate it, it is crucial to acquire a strong and long-lasting anti-SARS-CoV-2 immunity, by either natural infection or vaccination. We collected blood samples 12-305 days after positive polymerase chain reactions (PCRs) from 35 recovered individuals infected by SARS-CoV-2. Peripheral blood mononuclear cells were stimulated with SARS-CoV-2-derived peptide pools, such as the spike (S), nucleocapsid (N) and membrane (M) proteins, and we quantified anti-S immunoglobulins in plasma. After 10 months post-infection, we observed a sustained SARS-CoV-2-specific CD4+ T-cell response directed against M-protein, but responses against S- or N-proteins were lost over time. Besides, we demonstrated that O-group individuals presented significantly lower frequencies of specific CD4+ T-cell responses against Pep-M than non O-group individuals. The non O-group subjects also needed longer to clear the virus, and they lost cellular immune responses over time, compared to the O-group individuals, who showed a persistent specific immune response against SARS-CoV-2. Therefore, the S-specific immune response was lost over time, and individual factors might determine the sustainability of the body's defenses, which must be considered in the future design of vaccines to achieve continuous anti-SARS-CoV-2 immunity.</description><subject>ABO Blood-Group System</subject><subject>ABO group</subject><subject>COVID-19 - blood</subject><subject>Humans</subject><subject>humoral immune response</subject><subject>Immunity, Cellular</subject><subject>Immunity, Humoral</subject><subject>individual factors</subject><subject>Leukocytes, Mononuclear</subject><subject>Memory T Cells</subject><subject>memory T-cell response</subject><subject>Research Paper</subject><subject>SARS-CoV-2</subject><subject>SARS-CoV-2 - immunology</subject><subject>Spike Glycoprotein, Coronavirus</subject><issn>2150-5594</issn><issn>2150-5608</issn><issn>2150-5608</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2022</creationdate><recordtype>article</recordtype><sourceid>0YH</sourceid><sourceid>EIF</sourceid><sourceid>DOA</sourceid><recordid>eNp9UU1v3CAUtKpWTZTmJ6Ti2ItTwGCbS9XtKm0jRYqUpD3kgjA8NkTYOGBvtf--bHY3ai7lAO9jZt4TUxRnBJ8T3OLPlHDMuWDnFFOSLyIEF2-K42295DVu3x7iDDoqTlN6xPmwlmTa--KoYqJuaI2Pi_vFt2vU-RAMWsUwj8gl5IZ18GswOUDTA6CnWXk3bVCwz2kaQTvrNHJ9Pw-AIqQxDAmQGiZX3i5ubstl-F3SD8U7q3yC0_17Uvz6fnG3_FleXf-4XC6uSs0rNpVKWGygaoEaxgUhRFe2q7HgquasZoRb0uUGy5kRpq0YJtRy0nEQuGWUVCfF5U7XBPUox-h6FTcyKCefCyGupIqT0x5kR5pOm_xXoDtma6uw7SgjtMKQq8Cz1ped1jh3PRgNwxSVfyX6ujO4B7kKaykakRfbLvNpLxDD0wxpkr1LGrxXA4Q5SVoTzpqmFlWG8h1Ux5BSBPsyhmC5tVkebJZbm-Xe5sz7-O-OL6yDqRnwdQdwgw2xV39C9EZOauNDtFEN2iVZ_X_GX3n0tWg</recordid><startdate>20221231</startdate><enddate>20221231</enddate><creator>Gil-Manso, Sergio</creator><creator>Miguens Blanco, Iria</creator><creator>Motyka, Bruce</creator><creator>Halpin, Anne</creator><creator>López-Esteban, Rocío</creator><creator>Pérez-Fernández, Verónica Astrid</creator><creator>Carbonell, Diego</creator><creator>López-Fernández, Luis Andrés</creator><creator>West, Lori</creator><creator>Correa-Rocha, Rafael</creator><creator>Pion, Marjorie</creator><general>Taylor & Francis</general><general>Taylor & Francis Group</general><scope>0YH</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>7X8</scope><scope>5PM</scope><scope>DOA</scope><orcidid>https://orcid.org/0000-0003-1828-4745</orcidid><orcidid>https://orcid.org/0000-0003-2960-0301</orcidid><orcidid>https://orcid.org/0000-0001-7475-9245</orcidid><orcidid>https://orcid.org/0000-0002-8448-2777</orcidid><orcidid>https://orcid.org/0000-0002-1990-3651</orcidid><orcidid>https://orcid.org/0000-0003-3456-9986</orcidid><orcidid>https://orcid.org/0000-0003-2480-3628</orcidid></search><sort><creationdate>20221231</creationdate><title>ABO blood group is involved in the quality of the specific immune response anti-SARS-CoV-2</title><author>Gil-Manso, Sergio ; Miguens Blanco, Iria ; Motyka, Bruce ; Halpin, Anne ; López-Esteban, Rocío ; Pérez-Fernández, Verónica Astrid ; Carbonell, Diego ; López-Fernández, Luis Andrés ; West, Lori ; Correa-Rocha, Rafael ; Pion, Marjorie</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c534t-a9f0de38e2d459111c3fb6095a6546415f1b4594654d9d834012f51b5e9084213</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2022</creationdate><topic>ABO Blood-Group System</topic><topic>ABO group</topic><topic>COVID-19 - blood</topic><topic>Humans</topic><topic>humoral immune response</topic><topic>Immunity, Cellular</topic><topic>Immunity, Humoral</topic><topic>individual factors</topic><topic>Leukocytes, Mononuclear</topic><topic>Memory T Cells</topic><topic>memory T-cell response</topic><topic>Research Paper</topic><topic>SARS-CoV-2</topic><topic>SARS-CoV-2 - immunology</topic><topic>Spike Glycoprotein, Coronavirus</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Gil-Manso, Sergio</creatorcontrib><creatorcontrib>Miguens Blanco, Iria</creatorcontrib><creatorcontrib>Motyka, Bruce</creatorcontrib><creatorcontrib>Halpin, Anne</creatorcontrib><creatorcontrib>López-Esteban, Rocío</creatorcontrib><creatorcontrib>Pérez-Fernández, Verónica Astrid</creatorcontrib><creatorcontrib>Carbonell, Diego</creatorcontrib><creatorcontrib>López-Fernández, Luis Andrés</creatorcontrib><creatorcontrib>West, Lori</creatorcontrib><creatorcontrib>Correa-Rocha, Rafael</creatorcontrib><creatorcontrib>Pion, Marjorie</creatorcontrib><collection>Taylor & Francis 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>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><collection>DOAJ Directory of Open Access Journals</collection><jtitle>Virulence</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Gil-Manso, Sergio</au><au>Miguens Blanco, Iria</au><au>Motyka, Bruce</au><au>Halpin, Anne</au><au>López-Esteban, Rocío</au><au>Pérez-Fernández, Verónica Astrid</au><au>Carbonell, Diego</au><au>López-Fernández, Luis Andrés</au><au>West, Lori</au><au>Correa-Rocha, Rafael</au><au>Pion, Marjorie</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>ABO blood group is involved in the quality of the specific immune response anti-SARS-CoV-2</atitle><jtitle>Virulence</jtitle><addtitle>Virulence</addtitle><date>2022-12-31</date><risdate>2022</risdate><volume>13</volume><issue>1</issue><spage>30</spage><epage>45</epage><pages>30-45</pages><issn>2150-5594</issn><issn>2150-5608</issn><eissn>2150-5608</eissn><abstract>Since December 2019, the coronavirus disease 2019 (COVID-19), caused by the severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2), has spread throughout the world. To eradicate it, it is crucial to acquire a strong and long-lasting anti-SARS-CoV-2 immunity, by either natural infection or vaccination. We collected blood samples 12-305 days after positive polymerase chain reactions (PCRs) from 35 recovered individuals infected by SARS-CoV-2. Peripheral blood mononuclear cells were stimulated with SARS-CoV-2-derived peptide pools, such as the spike (S), nucleocapsid (N) and membrane (M) proteins, and we quantified anti-S immunoglobulins in plasma. After 10 months post-infection, we observed a sustained SARS-CoV-2-specific CD4+ T-cell response directed against M-protein, but responses against S- or N-proteins were lost over time. Besides, we demonstrated that O-group individuals presented significantly lower frequencies of specific CD4+ T-cell responses against Pep-M than non O-group individuals. The non O-group subjects also needed longer to clear the virus, and they lost cellular immune responses over time, compared to the O-group individuals, who showed a persistent specific immune response against SARS-CoV-2. Therefore, the S-specific immune response was lost over time, and individual factors might determine the sustainability of the body's defenses, which must be considered in the future design of vaccines to achieve continuous anti-SARS-CoV-2 immunity.</abstract><cop>United States</cop><pub>Taylor & Francis</pub><pmid>34967260</pmid><doi>10.1080/21505594.2021.2019959</doi><tpages>16</tpages><orcidid>https://orcid.org/0000-0003-1828-4745</orcidid><orcidid>https://orcid.org/0000-0003-2960-0301</orcidid><orcidid>https://orcid.org/0000-0001-7475-9245</orcidid><orcidid>https://orcid.org/0000-0002-8448-2777</orcidid><orcidid>https://orcid.org/0000-0002-1990-3651</orcidid><orcidid>https://orcid.org/0000-0003-3456-9986</orcidid><orcidid>https://orcid.org/0000-0003-2480-3628</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | ABO Blood-Group System ABO group COVID-19 - blood Humans humoral immune response Immunity, Cellular Immunity, Humoral individual factors Leukocytes, Mononuclear Memory T Cells memory T-cell response Research Paper SARS-CoV-2 SARS-CoV-2 - immunology Spike Glycoprotein, Coronavirus |
title | ABO blood group is involved in the quality of the specific immune response anti-SARS-CoV-2 |
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