<?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>2026-06-01T02:08:52Z</responseDate><request verb="GetRecord" identifier="oai:docta.ucm.es:20.500.14352/116260" metadataPrefix="oai_dc">https://docta.ucm.es/rest/oai/request</request><GetRecord><record><header><identifier>oai:docta.ucm.es:20.500.14352/116260</identifier><datestamp>2025-01-30T10:01:55Z</datestamp><setSpec>com_20.500.14352_14</setSpec><setSpec>col_20.500.14352_15</setSpec></header><metadata><oai_dc:dc xmlns:oai_dc="http://www.openarchives.org/OAI/2.0/oai_dc/" xmlns:dc="http://purl.org/dc/elements/1.1/" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xmlns:doc="http://www.lyncode.com/xoai" xsi:schemaLocation="http://www.openarchives.org/OAI/2.0/oai_dc/ http://www.openarchives.org/OAI/2.0/oai_dc.xsd">
   <dc:title>Immunogenicity of a third dose with mRNA-vaccines in the ChAdOx1-S/BNT162b2 vaccination regimen against SARS-CoV-2 variants</dc:title>
   <dc:creator>García Pérez, Javier</dc:creator>
   <dc:creator>Portolés Pérez, Antonio</dc:creator>
   <dc:creator>Pérez Ingidua, Carla</dc:creator>
   <dc:creator>Lora Pablos, David</dc:creator>
   <dc:creator>Gómez De La Cámara, Agustín Ramón</dc:creator>
   <dc:creator>Díez Fuertes, Francisco</dc:creator>
   <dc:creator>Ascaso del Río, Ana</dc:creator>
   <dc:subject>612.017</dc:subject>
   <dc:subject>614.2</dc:subject>
   <dc:subject>Inmunología</dc:subject>
   <dc:subject>Farmacología (Medicina)</dc:subject>
   <dc:subject>Enfermedades infecciosas</dc:subject>
   <dc:subject>3202 Epidemiología</dc:subject>
   <dc:subject>3212 Salud Publica</dc:subject>
   <dc:subject>3209 Farmacología</dc:subject>
   <dc:subject>2412 Inmunología</dc:subject>
   <dc:description>Summary
CombiVacS study has demonstrated a strong immune response of the heterologous ChAdOx1-S/BNT162b2 vaccine combination. The primary outcomes of the study were to assess the humoral immune response against SARS-CoV-2, 28 days after a third dose of a mRNA vaccine, in subjects that received a previous prime-boost scheme with ChAdOx1-S/BNT162b2. Secondary outcomes extended the study to 3 and 6 months. The third vaccine dose of mRNA-1273 in naive participants previously vaccinated with ChAdOx1-S/BNT162b2 regimen reached higher neutralizing antibodies titers against the variants of concern Delta and BA.1 lineage of Omicron compared with those receiving a third dose of BNT162b2 at day 28. These differences between BNT162b2 and mRNA-1273 arms were observed against the ancestral variant G614 at day 90. Suboptimal neutralizing response was observed against BQ.1.1, XBB.1.5/XBB.1.9, and JN.1 in a relevant proportion of individuals 180 days after the third dose, even after asymptomatic Omicron breakthrough infections. EudraCT (2021-001978-37); ClinicalTrials.gov (NCT04860739).</dc:description>
   <dc:description>Instituto de Salud Carlos III (España)</dc:description>
   <dc:description>Depto. de Enfermería</dc:description>
   <dc:description>Depto. de Farmacología y Toxicología</dc:description>
   <dc:description>Fac. de Enfermería, Fisioterapia y Podología</dc:description>
   <dc:description>Fac. de Medicina</dc:description>
   <dc:description>Fac. de Estudios Estadísticos</dc:description>
   <dc:description>TRUE</dc:description>
   <dc:description>pub</dc:description>
   <dc:date>2025-01-27T11:51:34Z</dc:date>
   <dc:date>2025-01-27T11:51:34Z</dc:date>
   <dc:date>2024-09-20</dc:date>
   <dc:type>journal article</dc:type>
   <dc:type>VoR</dc:type>
   <dc:identifier>https://hdl.handle.net/20.500.14352/116260</dc:identifier>
   <dc:identifier>2589-0042</dc:identifier>
   <dc:identifier>10.1016/j.isci.2024.110728</dc:identifier>
   <dc:language>eng</dc:language>
   <dc:relation>García-Pérez J, Borobia AM, Pérez-Olmeda M, Portoles A, Castaño L, Campins-Artí M, Bertrán MJ, Bermejo M, Arribas JM, López A, Ascaso-del-Rio A, Arana-Arri E, Fuentes Camps I, Vilella A, Cascajero A, García-Morales MT, Castillo de la Osa M, Pérez Ingidua C, Lora D, Jiménez-Santana P, Pino-Rosa S, Gómez de la Cámara A, De La Torre-Tarazona E, Calonge E, Cruces R, Belda-Iniesta C, Alcamí J, Frías J Carcas AJ, Díez-Fuertes F, * and CombiVacS Study Group. Immunogenicity of a third dose with mRNA-vaccines in the ChAdOx1-S/BNT162b2 vaccination regimen against SARS-CoV-2 variants. iScience. 2024 Sep; 27;9:110728. ISSN 2589-0042. https://doi.org/10.1016/j.isci.2024.110728.</dc:relation>
   <dc:rights>Attribution 4.0 International</dc:rights>
   <dc:rights>http://creativecommons.org/licenses/by/4.0/</dc:rights>
   <dc:rights>open access</dc:rights>
   <dc:format>application/pdf</dc:format>
   <dc:publisher>Elsevier</dc:publisher>
</oai_dc:dc></metadata></record></GetRecord></OAI-PMH>