<?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>2026-08-22T00:39:47Z</responseDate><request verb="GetRecord" identifier="oai:docta.ucm.es:20.500.14352/50380" metadataPrefix="oai_dc">https://docta.ucm.es/rest/oai/request</request><GetRecord><record><header><identifier>oai:docta.ucm.es:20.500.14352/50380</identifier><datestamp>2024-06-07T16:09:01Z</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>Elicitation from virus-naive individuals of cytotoxic T lymphocytes directed against conserved HIV-1 epitopes</dc:title>
   <dc:creator>Reche Gallardo, Pedro Antonio</dc:creator>
   <dc:creator>Keskin, Derin B</dc:creator>
   <dc:creator>Hussey, Rebecca E</dc:creator>
   <dc:creator>Ancuta, Petronela</dc:creator>
   <dc:creator>Gabuzda, Dana</dc:creator>
   <dc:creator>Reinherz, Ellis L</dc:creator>
   <dc:subject>612.017</dc:subject>
   <dc:subject>57:004</dc:subject>
   <dc:subject>Inmunología</dc:subject>
   <dc:subject>Microbiología (Biología)</dc:subject>
   <dc:subject>Biología molecular (Biología)</dc:subject>
   <dc:subject>Bioinformática</dc:subject>
   <dc:subject>2412 Inmunología</dc:subject>
   <dc:subject>2414 Microbiología</dc:subject>
   <dc:subject>2415 Biología Molecular</dc:subject>
   <dc:description>Cytotoxic T lymphocytes (CTL) protect against viruses including HIV-1. To avoid viral escape mutants that thwart immunity, we chose 25 CTL epitopes defined in the context of natural infection with functional and/or structural constraints that maintain sequence conservation. By combining HLA binding predictions with knowledge concerning HLA allele frequencies, a metric estimating population protection coverage (PPC) was computed and epitope pools assembled. Strikingly, only a minority of immunocompetent HIV-1 infected individuals responds to pools with PPC >95%. In contrast, virus-naive individuals uniformly expand IFNgamma producing cells and mount anti-HIV-1 cytolytic activity. This disparity suggests a vaccine design paradigm shift from infected to normal subjects.</dc:description>
   <dc:description>Depto. de Inmunología, Oftalmología y ORL</dc:description>
   <dc:description>Fac. de Medicina</dc:description>
   <dc:description>TRUE</dc:description>
   <dc:description>pub</dc:description>
   <dc:date>2023-06-20T09:48:05Z</dc:date>
   <dc:date>2023-06-20T09:48:05Z</dc:date>
   <dc:date>2006</dc:date>
   <dc:type>journal article</dc:type>
   <dc:identifier>https://hdl.handle.net/20.500.14352/50380</dc:identifier>
   <dc:identifier>1476-9433</dc:identifier>
   <dc:identifier>10.1186/1476-9433-5-1</dc:identifier>
   <dc:language>eng</dc:language>
   <dc:rights>Atribución 3.0 España</dc:rights>
   <dc:rights>https://creativecommons.org/licenses/by/3.0/es/</dc:rights>
   <dc:rights>open access</dc:rights>
   <dc:format>application/pdf</dc:format>
   <dc:publisher>BioMed Central</dc:publisher>
</oai_dc:dc></metadata></record></GetRecord></OAI-PMH>