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dc.contributor.authorTrujillo Vargas, Claudia Milena-
dc.contributor.authorGalletti, Jeremias G-
dc.contributor.authorScholand, Kaitlin K-
dc.contributor.authorYu, Zhiyuan-
dc.contributor.authorMauduit, Oliver-
dc.contributor.authorDelcroix, Vanessa-
dc.contributor.authorMakarenkova, Helen P-
dc.contributor.authorDe Paiva, Cintia S-
dc.date.accessioned2024-04-22T23:54:55Z-
dc.date.available2024-04-22T23:54:55Z-
dc.date.issued2023-
dc.identifier.citationGalletti JG, Scholand KK, Trujillo-Vargas CM, Yu Z, Mauduit O, Delcroix V, Makarenkova HP, de Paiva CS. Ectopic lymphoid structures in the aged lacrimal glands. Clin Immunol. 2023 Mar;248:109251. doi: 10.1016/j.clim.2023.109251.spa
dc.identifier.issn1521-6616-
dc.identifier.urihttps://hdl.handle.net/10495/39106-
dc.description.abstractABSTRACT: Aging is a complex biological process in which many organs are pathologically affected. We previously reported that aged C57BL/6J had increased lacrimal gland (LG) lymphoid infiltrates that suggest ectopic lymphoid structures. However, these ectopic lymphoid structures have not been fully investigated. Using C57BL/6J mice of different ages, we analyzed the transcriptome of aged murine LGs and characterized the B and T cell populations. Age-related changes in the LG include increased differentially expressed genes associated with B and T cell activation, germinal center formation, and infiltration by marginal zone-like B cells. We also identified an age-related increase in B1+ cells and CD19+B220+ cells. B220+CD19+ cells were GL7+ (germinal center-like) and marginal zone-like and progressively increased with age. There was an upregulation of transcripts related to T follicular helper cells, and the number of these cells also increased as mice aged. Compared to a mouse model of Sjögren syndrome, aged LGs have similar transcriptome responses but also unique ones. And lastly, the ectopic lymphoid structures in aged LGs are not exclusive to a specific mouse background as aged diverse outbred mice also have immune infiltration. Altogether, this study identifies a profound change in the immune landscape of aged LGs where B cells become predominant. Further studies are necessary to investigate the specific function of these B cells during the aged LGs.spa
dc.format.extent17 páginasspa
dc.format.mimetypeapplication/pdfspa
dc.language.isoengspa
dc.publisherElsevierspa
dc.publisherAcademic Pressspa
dc.type.hasversioninfo:eu-repo/semantics/publishedVersionspa
dc.rightsinfo:eu-repo/semantics/openAccessspa
dc.rights.urihttp://creativecommons.org/licenses/by/2.5/co/*
dc.titleEctopic lymphoid structures in the aged lacrimal glandsspa
dc.typeinfo:eu-repo/semantics/articlespa
dc.publisher.groupInmunodeficiencias Primariasspa
dc.identifier.doi10.1016/j.clim.2023.109251-
oaire.versionhttp://purl.org/coar/version/c_970fb48d4fbd8a85spa
dc.rights.accessrightshttp://purl.org/coar/access_right/c_abf2spa
dc.identifier.eissn1521-7035-
oaire.citationtitleClinical Immunologyspa
oaire.citationstartpage1spa
oaire.citationendpage17spa
oaire.citationvolume248spa
dc.rights.creativecommonshttps://creativecommons.org/licenses/by/4.0/spa
oaire.fundernameNational Eye Institutespa
dc.publisher.placeOrlando, Estados Unidosspa
dc.type.coarhttp://purl.org/coar/resource_type/c_2df8fbb1spa
dc.type.redcolhttps://purl.org/redcol/resource_type/ARTspa
dc.type.localArtículo de investigaciónspa
dc.subject.decsLinfocitos B-
dc.subject.decsB-Lymphocytes-
dc.subject.decsAparato Lagrimal-
dc.subject.decsLacrimal Apparatus-
dc.subject.decsTejido Linfoide-
dc.subject.decsLymphoid Tissue-
dc.subject.decsRatones Endogámicos C57BL-
dc.subject.decsMice, Inbred C57BL-
dc.subject.decsSíndrome de Sjögren-
dc.subject.decsSjogren's Syndrome-
dc.description.researchgroupidCOL0012426spa
oaire.awardnumberR01EY030447spa
dc.subject.meshurihttps://id.nlm.nih.gov/mesh/D001402-
dc.subject.meshurihttps://id.nlm.nih.gov/mesh/D007765-
dc.subject.meshurihttps://id.nlm.nih.gov/mesh/D008221-
dc.subject.meshurihttps://id.nlm.nih.gov/mesh/D008810-
dc.subject.meshurihttps://id.nlm.nih.gov/mesh/D012859-
dc.relation.ispartofjournalabbrevClin. Immunol.spa
oaire.funderidentifier.rorRoR:03wkg3b53-
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