Neutralizing antibody response after immunization with a COVID‐19 bivalent vaccine: Insights to the future
The raising of severe acute respiratory syndrome coronavirus 2 (SARS‐CoV‐2) variants led to the use of COVID‐19 bivalent vaccines, which include antigens of the wild‐type (WT) virus, and of the Omicron strain. In this study, we aimed to evaluate the impact of bivalent vaccination on the neutralizing...
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creator | Souza, Milena Silva Farias, Jéssica Pires Andreata‐Santos, Robert Silva, Marianne Pereira Brito, Ruth Dálety da Silva Duarte Barbosa da Silva, Marcia Peter, Cristina Mendes Cirilo, Marcus Vinícius de França Luiz, Wilson Barros Birbrair, Alexander Vidal, Paloma Oliveira Castro‐Amarante, Maria Fernanda Candido, Erika Donizetti Munhoz, Aldilene Silva Mello Malta, Fernanda Dorlass, Erik Gustavo Machado, Rafael Rahal Guaragna Pinho, João Renato Rebello Oliveira, Danielle Bruna Leal Durigon, Edison Luiz Maricato, Juliana Terzi Braconi, Carla Torres Ferreira, Luís Carlos de Souza Janini, Luiz Mário Ramos Amorim, Jaime Henrique |
description | The raising of severe acute respiratory syndrome coronavirus 2 (SARS‐CoV‐2) variants led to the use of COVID‐19 bivalent vaccines, which include antigens of the wild‐type (WT) virus, and of the Omicron strain. In this study, we aimed to evaluate the impact of bivalent vaccination on the neutralizing antibody (NAb) response. We enrolled 93 volunteers who had received three or four doses of monovalent vaccines based on the original virus (n = 61), or a booster shot with the bivalent vaccine (n = 32). Serum samples collected from volunteers were subjected to neutralization assays using the WT SARS‐CoV‐2, and Omicron subvariants. In addition, immunoinformatics to quantify and localize highly conserved NAb epitopes were performed. As main result, we observed that the neutralization titers of samples from individuals vaccinated with the bivalent vaccine were higher for the original virus, in comparison to their capacity of neutralizing the Omicron variant and its subvariants. NAb that recognize epitopes mostly conserved in the WT SARS‐CoV‐2 were boosted, while those that recognize epitopes mostly present in the Omicron variant, and subvariants were primed. These results indicate that formulation of future vaccines shall consider to target present viruses, and not viruses that no longer circulate. |
doi_str_mv | 10.1002/jmv.29416 |
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In this study, we aimed to evaluate the impact of bivalent vaccination on the neutralizing antibody (NAb) response. We enrolled 93 volunteers who had received three or four doses of monovalent vaccines based on the original virus (n = 61), or a booster shot with the bivalent vaccine (n = 32). Serum samples collected from volunteers were subjected to neutralization assays using the WT SARS‐CoV‐2, and Omicron subvariants. In addition, immunoinformatics to quantify and localize highly conserved NAb epitopes were performed. As main result, we observed that the neutralization titers of samples from individuals vaccinated with the bivalent vaccine were higher for the original virus, in comparison to their capacity of neutralizing the Omicron variant and its subvariants. NAb that recognize epitopes mostly conserved in the WT SARS‐CoV‐2 were boosted, while those that recognize epitopes mostly present in the Omicron variant, and subvariants were primed. These results indicate that formulation of future vaccines shall consider to target present viruses, and not viruses that no longer circulate.</description><identifier>ISSN: 0146-6615</identifier><identifier>ISSN: 1096-9071</identifier><identifier>EISSN: 1096-9071</identifier><identifier>DOI: 10.1002/jmv.29416</identifier><identifier>PMID: 38285457</identifier><language>eng</language><publisher>United States: Wiley Subscription Services, Inc</publisher><subject>Antibodies ; Antibody response ; Antigens ; bivalent vaccine ; boost ; Coronaviruses ; COVID-19 ; COVID-19 vaccines ; epitope ; Epitopes ; Immunization ; Neutralization ; Neutralizing ; Omicron ; SARS‐CoV‐2 ; Severe acute respiratory syndrome ; Severe acute respiratory syndrome coronavirus 2 ; Vaccines ; Viral diseases ; Viruses</subject><ispartof>Journal of medical virology, 2024-02, Vol.96 (2), p.e29416-n/a</ispartof><rights>2024 The Authors. published by Wiley Periodicals LLC.</rights><rights>2024 The Authors. Journal of Medical Virology published by Wiley Periodicals LLC.</rights><rights>2024. This article is published under http://creativecommons.org/licenses/by/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-c3886-ef3d4e7411ac986f39c83e01c94668d14c411325ce48a56f00b58b837abad1b43</citedby><cites>FETCH-LOGICAL-c3886-ef3d4e7411ac986f39c83e01c94668d14c411325ce48a56f00b58b837abad1b43</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1002%2Fjmv.29416$$EPDF$$P50$$Gwiley$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1002%2Fjmv.29416$$EHTML$$P50$$Gwiley$$Hfree_for_read</linktohtml><link.rule.ids>314,776,780,1411,27901,27902,45550,45551</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/38285457$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Souza, Milena Silva</creatorcontrib><creatorcontrib>Farias, Jéssica Pires</creatorcontrib><creatorcontrib>Andreata‐Santos, Robert</creatorcontrib><creatorcontrib>Silva, Marianne Pereira</creatorcontrib><creatorcontrib>Brito, Ruth Dálety da Silva</creatorcontrib><creatorcontrib>Duarte Barbosa da Silva, Marcia</creatorcontrib><creatorcontrib>Peter, Cristina Mendes</creatorcontrib><creatorcontrib>Cirilo, Marcus Vinícius de França</creatorcontrib><creatorcontrib>Luiz, Wilson Barros</creatorcontrib><creatorcontrib>Birbrair, Alexander</creatorcontrib><creatorcontrib>Vidal, Paloma Oliveira</creatorcontrib><creatorcontrib>Castro‐Amarante, Maria Fernanda</creatorcontrib><creatorcontrib>Candido, Erika Donizetti</creatorcontrib><creatorcontrib>Munhoz, Aldilene Silva</creatorcontrib><creatorcontrib>Mello Malta, Fernanda</creatorcontrib><creatorcontrib>Dorlass, Erik Gustavo</creatorcontrib><creatorcontrib>Machado, Rafael Rahal Guaragna</creatorcontrib><creatorcontrib>Pinho, João Renato Rebello</creatorcontrib><creatorcontrib>Oliveira, Danielle Bruna Leal</creatorcontrib><creatorcontrib>Durigon, Edison Luiz</creatorcontrib><creatorcontrib>Maricato, Juliana Terzi</creatorcontrib><creatorcontrib>Braconi, Carla Torres</creatorcontrib><creatorcontrib>Ferreira, Luís Carlos de Souza</creatorcontrib><creatorcontrib>Janini, Luiz Mário Ramos</creatorcontrib><creatorcontrib>Amorim, Jaime Henrique</creatorcontrib><title>Neutralizing antibody response after immunization with a COVID‐19 bivalent vaccine: Insights to the future</title><title>Journal of medical virology</title><addtitle>J Med Virol</addtitle><description>The raising of severe acute respiratory syndrome coronavirus 2 (SARS‐CoV‐2) variants led to the use of COVID‐19 bivalent vaccines, which include antigens of the wild‐type (WT) virus, and of the Omicron strain. 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subjects | Antibodies Antibody response Antigens bivalent vaccine boost Coronaviruses COVID-19 COVID-19 vaccines epitope Epitopes Immunization Neutralization Neutralizing Omicron SARS‐CoV‐2 Severe acute respiratory syndrome Severe acute respiratory syndrome coronavirus 2 Vaccines Viral diseases Viruses |
title | Neutralizing antibody response after immunization with a COVID‐19 bivalent vaccine: Insights to the future |
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