<?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>2026-06-08T09:32:18Z</responseDate><request verb="GetRecord" identifier="oai:docta.ucm.es:20.500.14352/101502" metadataPrefix="mods">https://docta.ucm.es/rest/oai/request</request><GetRecord><record><header><identifier>oai:docta.ucm.es:20.500.14352/101502</identifier><datestamp>2025-09-02T15:51:50Z</datestamp><setSpec>com_20.500.14352_14</setSpec><setSpec>col_20.500.14352_15</setSpec></header><metadata><mods:mods xmlns:mods="http://www.loc.gov/mods/v3" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xmlns:doc="http://www.lyncode.com/xoai" xsi:schemaLocation="http://www.loc.gov/mods/v3 http://www.loc.gov/standards/mods/v3/mods-3-1.xsd">
   <mods:name>
      <mods:namePart>Andreu-Ballester, Juan Carlos</mods:namePart>
   </mods:name>
   <mods:name>
      <mods:namePart>Galindo-Regal, Lorena</mods:namePart>
   </mods:name>
   <mods:name>
      <mods:namePart>Hidalgo-Coloma, Julia</mods:namePart>
   </mods:name>
   <mods:name>
      <mods:namePart>Cuéllar Del Hoyo, María Del Carmen</mods:namePart>
   </mods:name>
   <mods:name>
      <mods:namePart>García-Ballesteros, Carlos</mods:namePart>
   </mods:name>
   <mods:name>
      <mods:namePart>Hurtado, Carolina</mods:namePart>
   </mods:name>
   <mods:name>
      <mods:namePart>Uribe, Natalia</mods:namePart>
   </mods:name>
   <mods:name>
      <mods:namePart>Martín, María del Carmen</mods:namePart>
   </mods:name>
   <mods:name>
      <mods:namePart>Jiménez, Ana Isabel</mods:namePart>
   </mods:name>
   <mods:name>
      <mods:namePart>López-Chuliá, Francisca</mods:namePart>
   </mods:name>
   <mods:name>
      <mods:namePart>Llombart-Cussac, Antonio</mods:namePart>
   </mods:name>
   <mods:extension>
      <mods:dateAvailable encoding="iso8601">2024-02-16T11:02:52Z</mods:dateAvailable>
   </mods:extension>
   <mods:extension>
      <mods:dateAccessioned encoding="iso8601">2024-02-16T11:02:52Z</mods:dateAccessioned>
   </mods:extension>
   <mods:originInfo>
      <mods:dateIssued encoding="iso8601">2020</mods:dateIssued>
   </mods:originInfo>
   <mods:identifier type="citation">Andreu-Ballester JC, Galindo-Regal L, Hidalgo-Coloma J, Cuéllar C, García-Ballesteros C, Hurtado C, Uribe N, Del Carmen Martín M, Jiménez AI, López-Chuliá F, Llombart-Cussac A. Differences in circulating γδ T cells in patients with primary colon cancer and relation with prognostic factors. PLoS One. 2020 Dec 16;15(12):e0243545. doi: 10.1371/journal.pone.0243545. PMID: 33326443; PMCID: PMC7743935.</mods:identifier>
   <mods:identifier type="issn">1932-6203</mods:identifier>
   <mods:identifier type="doi">10.1371/journal.pone.0243545</mods:identifier>
   <mods:identifier type="uri">https://hdl.handle.net/20.500.14352/101502</mods:identifier>
   <mods:identifier type="officialurl">https://doi.org/10.1371/journal.pone.0243545</mods:identifier>
   <mods:abstract>Downregulation of the T cell system has been proposed as a mechanism to block immunity in colonic cancer (CC). However, little has been studied about circulating αβ and γδ T cells and their immunological status in newly diagnosed patients. The aim of this study was to characterize the αβ and γδ T cell subsets in peripheral blood of patients with CC matched with healthy volunteers. In this prospective case-control study, blood samples were obtained from 96 patients with newly diagnosed treatment-naïve infiltrating colonic adenocarcinoma and 48 healthy volunteers. Pathological report at surgery was obtained from all CC patients. A significant decrease in CD3+ γδ T cells and CD3+CD8+ γδ T cells (p&lt;0.001) were observed in CC patients. Apoptosis was significantly increased in all conventional and both αβ and γδ T cell subsets in patients with CC vs healthy subjects. γδ T cells were decreased in peripheral blood of patients with microscopic infiltration in tissues, history of cancer and synchronous colon cancer (p &lt; 0.05). IFN-γ was significantly reduced in CC patients compared to controls. Cytotoxic effector γδ T cells TEMRA (CD8 and CD56) are the proportionally most abundant T cells in peripheral blood of CC patients. Patients with CC present a deep downregulation in the systemic T-cell immunity. These variations are evident through all tumor stages and suggest that a deficiency in γδ T cell populations could be preventing control of tumor progression. This fact prove the role of immunomodulation on CC carcinogenesis.</mods:abstract>
   <mods:language>
      <mods:languageTerm>eng</mods:languageTerm>
   </mods:language>
   <mods:accessCondition type="useAndReproduction">http://creativecommons.org/licenses/by/4.0/</mods:accessCondition>
   <mods:accessCondition type="useAndReproduction">open access</mods:accessCondition>
   <mods:accessCondition type="useAndReproduction">Attribution 4.0 International</mods:accessCondition>
   <mods:titleInfo>
      <mods:title>Differences in circulating γδ T cells in patients with primary colon cancer and relation with prognostic factors</mods:title>
   </mods:titleInfo>
   <mods:genre>journal article</mods:genre>
</mods:mods></metadata></record></GetRecord></OAI-PMH>