<?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>2026-06-14T05:06:28Z</responseDate><request verb="GetRecord" identifier="oai:repisalud.isciii.es:20.500.12105/8959" metadataPrefix="marc">https://repisalud.isciii.es/rest/oai/request</request><GetRecord><record><header><identifier>oai:repisalud.isciii.es:20.500.12105/8959</identifier><datestamp>2024-09-27T23:16:22Z</datestamp><setSpec>com_20.500.12105_2052</setSpec><setSpec>com_20.500.12105_2051</setSpec><setSpec>col_20.500.12105_19609</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">Aragoneses-Fenoll, Laura</subfield>
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      <subfield code="a">Ojeda, Gloria</subfield>
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      <subfield code="a">Montes-Casado, Maria</subfield>
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      <subfield code="a">Acosta-Ampudia, Yeny</subfield>
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      <subfield code="a">Dianzani, Umberto</subfield>
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      <subfield code="a">Portoles, Pilar</subfield>
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      <subfield code="a">Rojo, José M</subfield>
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      <subfield code="c">2018</subfield>
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      <subfield code="a">Class IA phosphatidylinositol 3-kinase (PI3K) catalytic subunits p110α and p110δ are targets in cancer therapy expressed at high levels in T lymphocytes. The role of p110δ PI3K in normal or pathological immune responses is well established, yet the importance of p110α subunits in T cell-dependent immune responses is not clear. To address this problem, mice with p110α conditionally deleted in CD4+ and CD8+ T lymphocytes (p110α-/-ΔT) were used. p110α-/-ΔT mice show normal development of T cell subsets, but slightly reduced numbers of CD4+ T cells in the spleen. "In vitro," TCR/CD3 plus CD28 activation of naive CD4+ and CD8+ p110α-/-ΔT T cells showed enhanced effector function, particularly IFN-γ secretion, T-bet induction, and Akt, Erk, or P38 activation. Tfh derived from p110α-/-ΔT cells also have enhanced responses when compared to normal mice, and IL-2 expanded p110α-/-ΔT CD8+ T cells had enhanced levels of LAMP-1 and Granzyme B. By contrast, the expansion of p110α-/-ΔT iTreg cells was diminished. Also, p110α-/-ΔT mice had enhanced anti-keyhole limpet hemocyanin (KLH) IFN-γ, or IL-4 responses and IgG1 and IgG2b anti-KLH antibodies, using CFA or Alum as adjuvant, respectively. When compared to WT mice, p110α-/-ΔT mice inoculated with B16.F10 melanoma showed delayed tumor progression. The percentage of CD8+ T lymphocytes was higher and the percentage of Treg cells lower in the spleen of tumor-bearing p110α-/-ΔT mice. Also, IFN-γ production in tumor antigen-activated spleen cells was enhanced. Thus, PI3K p110α plays a significant role in antigen activation and differentiation of CD4+ and CD8+ T lymphocytes modulating antitumor immunity.</subfield>
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      <subfield code="a">Front Immunol. 2018 Feb 27;9:332.</subfield>
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      <subfield code="a">10.3389/fimmu.2018.00332</subfield>
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      <subfield code="a">1664-3224</subfield>
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      <subfield code="a">Frontiers in immunology</subfield>
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      <subfield code="a">29535720</subfield>
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      <subfield code="a">http://hdl.handle.net/20.500.12105/8959</subfield>
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      <subfield code="a">CD28 costimulation</subfield>
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      <subfield code="a">PI3-kinase alpha subunit</subfield>
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      <subfield code="a">PI3K</subfield>
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      <subfield code="a">T lymphocytes</subfield>
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      <subfield code="a">Anti-KLH response</subfield>
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      <subfield code="a">Melanoma</subfield>
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   <datafield ind2="0" ind1="0" tag="245">
      <subfield code="a">T-Cell-Specific Loss of the PI-3-Kinase p110α Catalytic Subunit Results in Enhanced Cytokine Production and Antitumor Response</subfield>
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