<?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>2026-06-29T09:28:11Z</responseDate><request verb="GetRecord" identifier="oai:docta.ucm.es:20.500.14352/106814" metadataPrefix="oai_dc">https://docta.ucm.es/rest/oai/request</request><GetRecord><record><header><identifier>oai:docta.ucm.es:20.500.14352/106814</identifier><datestamp>2025-03-18T12:43:32Z</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>A Low Number of Baselines γδ T Cells Increases the Risk of SARS-CoV-2 Post-Vaccination Infection</dc:title>
   <dc:creator>Andreu-Ballester, Juan Carlos</dc:creator>
   <dc:creator>Galindo-Regal, Lorena</dc:creator>
   <dc:creator>Cuéllar Del Hoyo, María Del Carmen</dc:creator>
   <dc:creator>López-Chuliá, Francisca</dc:creator>
   <dc:creator>García-Ballesteros, Carlos</dc:creator>
   <dc:creator>Fernández-Murga, Leonor</dc:creator>
   <dc:creator>Llombart-Cussac, Antonio</dc:creator>
   <dc:creator>Domínguez-Márquez, María Victoria</dc:creator>
   <dc:contributor>Klasse, P. J.</dc:contributor>
   <dc:contributor>Mostafa, Mai</dc:contributor>
   <dc:subject>579.6</dc:subject>
   <dc:subject>615.28</dc:subject>
   <dc:subject>576.8</dc:subject>
   <dc:subject>SARS-CoV-2</dc:subject>
   <dc:subject>vaccine</dc:subject>
   <dc:subject>antibodies</dc:subject>
   <dc:subject>αβ T cells</dc:subject>
   <dc:subject>γδ T cells</dc:subject>
   <dc:subject>Microbiología (Farmacia)</dc:subject>
   <dc:subject>Parasitología (Farmacia)</dc:subject>
   <dc:subject>32 Ciencias Médicas</dc:subject>
   <dc:subject>3207.12 Parasitología</dc:subject>
   <dc:description>Background: The COVID-19 pandemic is the biggest global health problem in the last hundred years. The efficacy of the vaccine to protect against severe disease is estimated to be 70–95% according to the studies carried out, although there are aspects of the immune response to the vaccine that remain unclear. Methods: Humoral and cellular immunity after the administration of three doses of the Pfizer–BioNTech and Oxford AstraZeneca vaccines against SARS-CoV-2 over one year and the appearance of post-vaccination COVID-19 were studied. SARS-CoV-2 IgG and IgA antibodies, αβ and γδ T-cell subsets, and their differentiation stages and apoptosis were analyzed. Results: Anti-SARS-CoV-2 IgG and IgA antibodies showed a progressive increase throughout the duration of the study. This increase was the greatest after the third dose. The highest levels were observed in subjects who had anti-SARS-CoV-2 antibodies prior to vaccination. There was an increase in CD4+ αβ, CD8+ γδ and TEM CD8+ γδ T cells, and a decrease in apoptosis in CD4+ CD8+ and CD56+ αβ and γδ T cells. Post-vaccination SARS-CoV-2 infection was greater than 60%. The symptoms of COVID-19 were very mild and were related to a γδ T cell deficit, specifically CD8+ TEMRA and CD56+ γδ TEM, as well as lower pre-vaccine apoptosis levels. Conclusions: The results unveil the important role of γδ T cells in SARS-CoV-2-vaccine-mediated protection from the disease.</dc:description>
   <dc:description>REACT-EU programme</dc:description>
   <dc:description>Consellería de Sanitat Universal i Salut Pública (Generalitat Valenciana, Spain)</dc:description>
   <dc:description>Depto. de Microbiología y Parasitología</dc:description>
   <dc:description>Fac. de Farmacia</dc:description>
   <dc:description>TRUE</dc:description>
   <dc:description>pub</dc:description>
   <dc:description>Pagado por el autor</dc:description>
   <dc:date>2024-07-17T11:36:49Z</dc:date>
   <dc:date>2024-07-17T11:36:49Z</dc:date>
   <dc:date>2024-05-18</dc:date>
   <dc:type>journal article</dc:type>
   <dc:type>VoR</dc:type>
   <dc:identifier>https://hdl.handle.net/20.500.14352/106814</dc:identifier>
   <dc:identifier>2076-393X</dc:identifier>
   <dc:identifier>10.3390/vaccines12050553</dc:identifier>
   <dc:language>eng</dc:language>
   <dc:relation>Andreu-Ballester, Juan Carlos, et al. «A Low Number of Baselines Γδ T Cells Increases the Risk of SARS-CoV-2 Post-Vaccination Infection». Vaccines, vol. 12, n.o 5, mayo de 2024, p. 553. www.mdpi.com, https://doi.org/10.3390/vaccines12050553.</dc:relation>
   <dc:rights>Attribution-NonCommercial-NoDerivatives 4.0 International</dc:rights>
   <dc:rights>http://creativecommons.org/licenses/by-nc-nd/4.0/</dc:rights>
   <dc:rights>open access</dc:rights>
   <dc:format>application/pdf</dc:format>
   <dc:publisher>MDPI</dc:publisher>
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