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dc.creatorVarona, Rosa-
dc.creatorVillares, Ricardo-
dc.creatorCarramolino, Laura-
dc.creatorGoya, Íñigo-
dc.date2008-04-16T08:58:39Z-
dc.date2008-04-16T08:58:39Z-
dc.date2001-03-
dc.date.accessioned2017-01-31T01:02:25Z-
dc.date.available2017-01-31T01:02:25Z-
dc.identifierThe Journal of Clinical Investigation,vol. 107, 2001, March, pp. R37-45-
dc.identifier0021-9738-
dc.identifierhttp://hdl.handle.net/10261/3607-
dc.identifier.urihttp://dspace.mediu.edu.my:8181/xmlui/handle/10261/3607-
dc.descriptionEl copyright pertenece a The American Society for Clinical Investigation-
dc.descriptionCCR6 expression in dendritic, T, and B cells suggests that this b-chemokine receptor may regulate the migration and recruitment of antigen-presenting and immunocompetent cells during inflammatory and immunological responses. Here we demonstrate that CCR6–/– mice have underdeveloped Peyer’s patches, in which the myeloid CD11b+ CD11c+ dendritic-cell subset is not present in the subepithelial dome. CCR6–/– mice also have increased numbers in T-cell subpopulations within the intestinal mucosa. In 2,4-dinitrofluorobenzene–induced contact hypersensitivity (CHS) studies, CCR6–/– mice developed more severe and more persistent inflammation than wild-type (WT) animals. Conversely, in a delayedtype hypersensitivity (DTH) model induced with allogeneic splenocytes, CCR6–/– mice developed no inflammatory response. The altered responses seen in the CHS and DTH assays suggest the existence of a defect in the activation and/or migration of the CD4+ T-cell subsets that downregulate or elicit the inflammation response, respectively. These findings underscore the role of CCR6 in cutaneous and intestinal immunity and the utility of CCR6–/– mice as a model to study pathologies in these tissues.-
dc.descriptionPeer reviewed-
dc.format1804153 bytes-
dc.formatapplication/pdf-
dc.languageeng-
dc.publisherAmerican Society for Clinical Investigation-
dc.rightsopenAccess-
dc.titleCCR6-deficient mice have impaired leukocyte homeostasis and altered contact hypersensitivity and delayed-type hypersensitivity responses-
dc.typeArtículo-
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