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dc.contributor.authorPerdomo Celis, Federico-
dc.contributor.authorTaborda Vanegas, Natalia Andrea-
dc.contributor.authorRugeles López, María Teresa-
dc.date.accessioned2023-03-14T22:35:43Z-
dc.date.available2023-03-14T22:35:43Z-
dc.date.issued2017-
dc.identifier.urihttps://hdl.handle.net/10495/34010-
dc.description.abstractABSTRACT: The lymphoid follicle is critical for the development of humoral immune responses. Cell circulation to this site is highly regulated by the differential expression of chemokine receptors. This feature contributes to the establishment of viral reservoirs in lymphoid follicles and the development of some types of malignancies that are able to evade immune surveillance, especially conventional CD8+ T cells. Interestingly, a subtype of CD8+ T cells located within the lymphoid follicle (follicular CD8+ T cells) was recently described; these cells have been proposed to play an important role in viral and tumor control, as well as to modulate humoral and T follicular helper cell responses. In this review, we summarize the knowledge on this novel CD8+ T cell population, its origin, function, and potential role in health and disease, in particular, in the context of the infection by the human immunodeficiency virus.spa
dc.format.extent13spa
dc.format.mimetypeapplication/pdfspa
dc.language.isoengspa
dc.publisherFrontiers Research Foundationspa
dc.type.hasversioninfo:eu-repo/semantics/publishedVersionspa
dc.rightsinfo:eu-repo/semantics/openAccessspa
dc.rights.urihttp://creativecommons.org/licenses/by/2.5/co/*
dc.titleFollicular CD8 + T Cells : Origin, Fuction and Importance During HIV Infectionspa
dc.typeinfo:eu-repo/semantics/articlespa
dc.publisher.groupInmunovirologíaspa
dc.identifier.doi10.3389/fimmu.2017.01241-
oaire.versionhttp://purl.org/coar/version/c_970fb48d4fbd8a85spa
dc.rights.accessrightshttp://purl.org/coar/access_right/c_abf2spa
dc.identifier.eissn1664-3224-
oaire.citationtitleFrontiers in Immunologyspa
oaire.citationstartpage1spa
oaire.citationendpage13spa
oaire.citationvolume8spa
oaire.citationissue1241spa
thesis.degree.disciplinesin facultad - programaspa
dc.rights.creativecommonshttps://creativecommons.org/licenses/by/4.0/spa
dc.publisher.placeLausana, Suizaspa
dc.type.coarhttp://purl.org/coar/resource_type/c_dcae04bcspa
dc.type.redcolhttps://purl.org/redcol/resource_type/ARTREVspa
dc.type.localArtículo de revisiónspa
dc.subject.decsLinfocitos T-
dc.subject.decsT-Lymphocytes-
dc.subject.decsLinfocitos B-
dc.subject.decsB-Lymphocytes-
dc.subject.decsT-Lymphocytes, Cytotoxic-
dc.subject.decsLinfocitos T Citotóxicos-
dc.subject.decsCD8 Antigens-
dc.subject.decsAntígenos CD8-
dc.subject.decsReceptors, CXCR5-
dc.subject.decsReceptores CXCR5-
dc.identifier.urlhttps://www.frontiersin.org/articles/10.3389/fimmu.2017.01241/fullspa
dc.description.researchgroupidCOL0012444spa
dc.relation.ispartofjournalabbrevFront. Immunol.spa
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