Mostrar el registro sencillo del ítem
dc.contributor.author | Galindo-Albarrán, Ariel O | |
dc.contributor.author | López-Portales, Oscar H | |
dc.contributor.author | Gutiérrez-Reyna, Darely Y | |
dc.contributor.author | Rodríguez-Jorge, Otoniel | |
dc.contributor.author | Sánchez-Villanueva, José Antonio | |
dc.contributor.author | Ramírez-Pliego, Oscar | |
dc.contributor.author | Bergon, Aurélie | |
dc.contributor.author | Loriod, Béatrice | |
dc.contributor.author | Holota, Hélène | |
dc.contributor.author | Imbert, Jean | |
dc.contributor.author | Hernández-Mendoza, Armando | |
dc.contributor.author | Ferrier, Pierre | |
dc.contributor.author | Carrillo-de Santa Pau, Enrique | |
dc.contributor.author | Valencia, Alfonso | |
dc.contributor.author | Spicuglia, Salvatore | |
dc.contributor.author | Santana, M Angélica | |
dc.date.accessioned | 2019-07-12T09:31:22Z | |
dc.date.available | 2019-07-12T09:31:22Z | |
dc.date.issued | 2016-11-15 | |
dc.identifier.citation | Cell Rep. 2016;17(8):2151-2160. | es_ES |
dc.identifier.issn | 22111247 | es_ES |
dc.identifier.uri | http://hdl.handle.net/20.500.12105/7900 | |
dc.description.abstract | To better understand why human neonates show a poor response to intracellular pathogens, we compared gene expression and histone modification profiles of neonatal naive CD8+ T cells with that of their adult counterparts. We found that neonatal lymphocytes have a distinct epigenomic landscape associated with a lower expression of genes involved in T cell receptor (TCR) signaling and cytotoxicity and a higher expression of genes involved in the cell cycle and innate immunity. Functional studies corroborated that neonatal CD8+ T cells are less cytotoxic, transcribe antimicrobial peptides, and produce reactive oxygen species. Altogether, our results show that neonatal CD8+ T cells have a specific genetic program biased toward the innate immune response. These findings will contribute to better diagnosis and management of the neonatal immune response. | es_ES |
dc.description.sponsorship | This project was specifically supported by a joint EcosNord-Anuies-SEP-Con-acyt project (M11S01). Work in the M.A.S. laboratory is supported by grantsfrom Consejo Nacional de Ciencia y Tecnologı ́a(CONACYT; CB-2011-01168182) and Programa de Mejoramiento del Profesorado (PROMEPSI-UAEM/13/342). Work in the S.S. laboratory is supported by recurrent fundingfrom the Inserm and Aix-Marseille University and by specific grants from theEuropean Union’s FP7 Program (agreement 282510-BLUEPRINT), the Associ-ation pour la Recherche contre le Cancer (ARC) (project SFI20111203756), andthe Aix-Marseille initiative d’excelence (A*MIDEX) project ANR-11-IDEX-0001-02. We thank Centro Estatal de la Transfusio ́n Sanguı ́nea in Cuernavaca for thedonation of leukocyte concentrates and the mothers and babies of HospitalGeneral Parres in Cuernavaca for the donation of cord blood. This study makesuse of data generated by the Blueprint and Roadmap consortia. A full list of theinvestigators who contributed to the generation of the data is availablefromwww.blueprint-epigenome.euandhttp://www.roadmapepigenomics.org/. Funding for the Blueprint project was provided by the European Union’sSeventh Framework Program (FP7/2007-2013) under grant agreement282510 – BLUEPRINT. The Roadmap consortium is financed by the NIH. Weare grateful to Professor C.I. Pogson for critical reading of the manuscript. | es_ES |
dc.language.iso | eng | es_ES |
dc.publisher | Elsevier | es_ES |
dc.type.hasVersion | VoR | es_ES |
dc.rights.uri | http://creativecommons.org/licenses/by-nc-sa/4.0/ | * |
dc.subject | T lymphocyte | es_ES |
dc.subject | Epigenome | es_ES |
dc.subject | Human immunity | es_ES |
dc.subject | Immune response | es_ES |
dc.subject.mesh | Adult | es_ES |
dc.subject.mesh | CD8-Positive T-Lymphocytes | es_ES |
dc.subject.mesh | Cytotoxicity, Immunologic | es_ES |
dc.subject.mesh | Epigenesis, Genetic | es_ES |
dc.subject.mesh | Gene Expression Profiling | es_ES |
dc.subject.mesh | Gene Expression Regulation, Developmental | es_ES |
dc.subject.mesh | Humans | es_ES |
dc.subject.mesh | Immunity, Innate | es_ES |
dc.subject.mesh | Infant, Newborn | es_ES |
dc.subject.mesh | Transcription Factors | es_ES |
dc.title | CD8+ T Cells from Human Neonates Are Biased toward an Innate Immune Response | es_ES |
dc.type | journal article | es_ES |
dc.rights.license | Atribución-NoComercial-CompartirIgual 4.0 Internacional | * |
dc.identifier.pubmedID | 27851975 | es_ES |
dc.format.volume | 17 | es_ES |
dc.format.number | 8 | es_ES |
dc.format.page | 2151-2160 | es_ES |
dc.identifier.doi | 10.1016/j.celrep.2016.10.056 | es_ES |
dc.contributor.funder | Consejo Nacional de Ciencia y Tecnología (México) | |
dc.contributor.funder | Unión Europea. Comisión Europea. European Research Council (ERC) | |
dc.contributor.funder | Programa de Mejoramiento del Profesorado | |
dc.contributor.funder | Aix-Marseille University (Francia) | |
dc.contributor.funder | Fondation ARC pour la recherche sur le cancer | |
dc.description.peerreviewed | Sí | es_ES |
dc.identifier.e-issn | 2211-1247 | es_ES |
dc.relation.publisherversion | https://doi.org/10.1016/j.celrep.2016.10.056. | es_ES |
dc.identifier.journal | Cell reports | es_ES |
dc.repisalud.institucion | CNIO | es_ES |
dc.repisalud.orgCNIO | CNIO::Grupos de investigación::Grupo de Biología Computacional Estructural | es_ES |
dc.relation.projectID | info:eu-repo/grantAgreement/EC/FP7/282510 | es_ES |
dc.rights.accessRights | open access | es_ES |