<?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>2026-04-23T21:10:36Z</responseDate><request verb="GetRecord" identifier="oai:uvadoc.uva.es:10324/81890" metadataPrefix="mods">https://uvadoc.uva.es/oai/request</request><GetRecord><record><header><identifier>oai:uvadoc.uva.es:10324/81890</identifier><datestamp>2026-04-15T06:37:24Z</datestamp><setSpec>com_10324_1134</setSpec><setSpec>com_10324_931</setSpec><setSpec>com_10324_894</setSpec><setSpec>col_10324_1213</setSpec></header><metadata><mods:mods xmlns:mods="http://www.loc.gov/mods/v3" xmlns:doc="http://www.lyncode.com/xoai" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xsi:schemaLocation="http://www.loc.gov/mods/v3 http://www.loc.gov/standards/mods/v3/mods-3-1.xsd">
<mods:name>
<mods:namePart>Aparicio Fernández, Cristina</mods:namePart>
</mods:name>
<mods:name>
<mods:namePart>Queipo Riera, Mónica</mods:namePart>
</mods:name>
<mods:name>
<mods:namePart>Belver, Marina</mods:namePart>
</mods:name>
<mods:name>
<mods:namePart>Espeso, Francisco</mods:namePart>
</mods:name>
<mods:name>
<mods:namePart>Serna Pérez, Julia</mods:namePart>
</mods:name>
<mods:name>
<mods:namePart>Enríquez Rodríguez, Lucía</mods:namePart>
</mods:name>
<mods:name>
<mods:namePart>Acebal, Carlos</mods:namePart>
</mods:name>
<mods:name>
<mods:namePart>Martín Muñoz, Álvaro</mods:namePart>
</mods:name>
<mods:name>
<mods:namePart>Valeri, Antonio</mods:namePart>
</mods:name>
<mods:name>
<mods:namePart>Leivas, Alejandra</mods:namePart>
</mods:name>
<mods:name>
<mods:namePart>Río, Paula</mods:namePart>
</mods:name>
<mods:name>
<mods:namePart>Powell, Daniel J.</mods:namePart>
</mods:name>
<mods:name>
<mods:namePart>Lobo Valentín, Rosa María</mods:namePart>
</mods:name>
<mods:name>
<mods:namePart>Arrabal, David</mods:namePart>
</mods:name>
<mods:name>
<mods:namePart>Martínez López, Joaquín</mods:namePart>
</mods:name>
<mods:name>
<mods:namePart>Sánchez, Ana</mods:namePart>
</mods:name>
<mods:name>
<mods:namePart>Fuente García, Miguel Ángel de la</mods:namePart>
</mods:name>
<mods:name>
<mods:namePart>González-Vallinas Garrachón, Margarita</mods:namePart>
</mods:name>
<mods:extension>
<mods:dateAvailable encoding="iso8601">2026-01-20T15:42:57Z</mods:dateAvailable>
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<mods:dateAccessioned encoding="iso8601">2026-01-20T15:42:57Z</mods:dateAccessioned>
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<mods:originInfo>
<mods:dateIssued encoding="iso8601">2025</mods:dateIssued>
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<mods:identifier type="citation">Cancers,  2025, vol. 17, n. 19, p. 3186.</mods:identifier>
<mods:identifier type="issn">2072-6694</mods:identifier>
<mods:identifier type="uri">https://uvadoc.uva.es/handle/10324/81890</mods:identifier>
<mods:identifier type="doi">10.3390/cancers17193186</mods:identifier>
<mods:identifier type="publicationfirstpage">3186</mods:identifier>
<mods:identifier type="publicationissue">19</mods:identifier>
<mods:identifier type="publicationtitle">Cancers</mods:identifier>
<mods:identifier type="publicationvolume">17</mods:identifier>
<mods:identifier type="essn">2072-6694</mods:identifier>
<mods:abstract>Chimeric Antigen Receptor (CAR)-T cell therapy has shown significant success in treating hematological cancers, but commercialized autologous CAR-T therapies face challenges such as high costs, manufacturing delays, complex standardization and the risk of tumor relapses due to single-antigen targeting. To address these issues, a novel allogeneic CAR-T therapy with broader target specificity was developed, optimizing its manufacturing process. Using CRISPR/Cas9, TCR and HLA class I complex expression were eliminated from donor T cells to reduce the risk of immune rejection and graft-versus-host disease. Additionally, NKG2D CAR, targeting eight ligands upregulated in both solid and hematological tumors, was lentivirally transduced. This study optimized CAR-T cell manufacture&#xd;
by testing various interleukin supplements (IL-2, IL-7/IL-15, IL-7/IL-15/IL-21). Results showed that IL-7/IL-15/IL-21 supplementation produced CAR-T cells with the most suitable characteristics in terms of genetic modification efficiency, cell proliferation, antitumor activity and memory profile. This new allogeneic NKG2D CAR-T therapy represents a promising universal treatment for a variety of cancers.</mods:abstract>
<mods:language>
<mods:languageTerm>eng</mods:languageTerm>
</mods:language>
<mods:accessCondition type="useAndReproduction">info:eu-repo/semantics/openAccess</mods:accessCondition>
<mods:accessCondition type="useAndReproduction">http://creativecommons.org/licenses/by-nc-nd/4.0/</mods:accessCondition>
<mods:accessCondition type="useAndReproduction">Attribution-NonCommercial-NoDerivatives 4.0 Internacional</mods:accessCondition>
<mods:titleInfo>
<mods:title>A novel early memory-enriched allogeneic NKG2D CAR-T cell therapy based on CRISPR/Cas9 technology for solid tumors</mods:title>
</mods:titleInfo>
<mods:genre>info:eu-repo/semantics/article</mods:genre>
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