Transcription of the unique ruminant class II major histocompatibility complex-DYA and DIB genes in dendritic cells

cg.identifier.doihttps://doi.org/10.1002/1521-4141(200101)31:1<82en
cg.issn0014-2980en
cg.issue1en
cg.journalEuropean Journal of Immunologyen
cg.subject.ilriVACCINESen
cg.subject.ilriGENETICSen
cg.volume31en
dc.contributor.authorBallingall, Keith T.en
dc.contributor.authorMacHugh, Niall D.en
dc.contributor.authorTaracha, E.L.N.en
dc.contributor.authorMertens, B.en
dc.contributor.authorMcKeever, B.D.en
dc.date.accessioned2013-07-03T05:25:44Zen
dc.date.available2013-07-03T05:25:44Zen
dc.identifier.urihttps://hdl.handle.net/10568/32905
dc.titleTranscription of the unique ruminant class II major histocompatibility complex-DYA and DIB genes in dendritic cellsen
dcterms.abstractDendritic cells (DC) constitute the most effective immune cell population for priming and recalling T cell responses to foreign antigens. DC patrol the peripheral tissues collecting foreign antigen for subsequent presentation by classical class II MHC molecules to T cells in the draining lymph nodes. Since the description of the DYA and DIB class II MHC genes, which are unique to ruminants, no transcript or protein have been reported. Here we provide evidence that these genes are transcribed in cattle and that paired transcription is restricted in afferent lymph to a functionally distinct population of DC. Analysis of lymph node, lung and thymus suggests that tissue DC also transcribe both genes. Cytokine-induced differentiation of cultured monocytes to a DC phenotype is linked with induction of both DYA and DIB transcription. This is consistent with an association of their products with the potent antigen presenting capacity of these cells in cattle.en
dcterms.accessRightsLimited Access
dcterms.bibliographicCitationEuropean Journal of Immunology;31(1): 82-86en
dcterms.extentp. 82-86en
dcterms.issued2001
dcterms.languageen
dcterms.publisherWileyen
dcterms.subjectveterinary medicineen
dcterms.subjectimmunologyen
dcterms.subjectmajor histocompatibility complexen
dcterms.subjectcellsen
dcterms.typeJournal Article

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