<?xml version="1.0" encoding="UTF-8"?><?xml-stylesheet type="text/xsl" href="static/style.xsl"?><OAI-PMH xmlns="http://www.openarchives.org/OAI/2.0/" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xsi:schemaLocation="http://www.openarchives.org/OAI/2.0/ http://www.openarchives.org/OAI/2.0/OAI-PMH.xsd"><responseDate>2026-08-29T12:37:53Z</responseDate><request verb="GetRecord" identifier="oai:repisalud.isciii.es:20.500.12105/16083" metadataPrefix="marc">https://repisalud.isciii.es/rest/oai/request</request><GetRecord><record><header><identifier>oai:repisalud.isciii.es:20.500.12105/16083</identifier><datestamp>2024-11-28T17:32:56Z</datestamp><setSpec>com_20.500.12105_2052</setSpec><setSpec>com_20.500.12105_2051</setSpec><setSpec>com_20.500.12105_15322</setSpec><setSpec>col_20.500.12105_19609</setSpec><setSpec>col_20.500.12105_16961</setSpec><setSpec>col_20.500.12105_16964</setSpec></header><metadata><record xmlns="http://www.loc.gov/MARC21/slim" xmlns:dcterms="http://purl.org/dc/terms/" xmlns:doc="http://www.lyncode.com/xoai" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xsi:schemaLocation="http://www.loc.gov/MARC21/slim http://www.loc.gov/standards/marcxml/schema/MARC21slim.xsd">
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      <subfield code="a">García-Pérez, Javier</subfield>
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      <subfield code="a">Bermejo, Mercedes</subfield>
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      <subfield code="a">Ramírez-García, Almudena</subfield>
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      <subfield code="a">de la Torre-Tarazona, Humberto Erick</subfield>
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      <subfield code="a">Cascajero Díaz, Almudena</subfield>
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      <subfield code="a">Payares-Herrera, Concepción</subfield>
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      <subfield code="a">Vicente-Izquierdo, Laura</subfield>
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      <subfield code="a">Avendaño-Solá, Cristina</subfield>
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      <subfield code="a">Alcamí, José</subfield>
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      <subfield code="a">Perez-Olmeda, Mayte</subfield>
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      <subfield code="a">Díez-Fuertes, Francisco</subfield>
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      <subfield code="c">2023-03</subfield>
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      <subfield code="a">The humoral immune response against severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) variants of concern elicited by vaccination was evaluated in COVID-19 recovered individuals (Rec) separated 1-3 months (Rec2m) or 4-12 months (Rec9m) postinfection and compared to the response in naïve participants. Antibody-mediated immune responses were assessed in 66 participants by three commercial immunoassays and a SARS-CoV-2 lentiviral-based pseudovirus neutralization assay. Immunoglobulin (Ig) levels against SARS-CoV-2 spike were lower in naïve participants after two doses than in Rec after a single dose (p &lt; 0.05). After two doses in Rec, levels of total Ig to receptor-binding domain were significantly increased in Rec9m compared to Rec2m (p &lt; 0.001). The neutralizing potency observed in Rec9m was consistently higher than in Rec2m against variants of concern (VOCs) Alpha, Beta, Delta, and BA.1 sublineage of Omicron with 2.2-2.8-fold increases. Increasing the interval between SARS-CoV-2 infection and the vaccination with messenger RNA-based vaccines to more than 3 months generates a more efficient heterologous humoral immune response against VOCs by allowing enough time to mount a strong recall memory B cell response.</subfield>
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      <subfield code="a">J Med Virol. 2023 Mar;95(3):e28679.</subfield>
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      <subfield code="a">10.1002/jmv.28679</subfield>
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      <subfield code="a">1096-9071</subfield>
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      <subfield code="a">Journal of medical virology</subfield>
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      <subfield code="a">36929737</subfield>
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      <subfield code="a">http://hdl.handle.net/20.500.12105/16083</subfield>
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      <subfield code="a">Omicron</subfield>
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      <subfield code="a">Hybrid immunity</subfield>
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      <subfield code="a">Timing of vaccination</subfield>
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      <subfield code="a">Longer intervals between SARS-CoV-2 infection and mRNA-1273 doses improve the neutralization of different variants of concern</subfield>
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