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http://purl.uniprot.org/citations/20971950http://www.w3.org/1999/02/22-rdf-syntax-ns#typehttp://purl.uniprot.org/core/Journal_Citation
http://purl.uniprot.org/citations/20971950http://www.w3.org/2000/01/rdf-schema#comment"The interleukin (IL)-22R1 chain of the heterodimeric IL-22 receptor is not expressed on normal leukocytes, but this receptor is expressed on T cells from anaplastic lymphoma kinase-positive (ALK(+)) anaplastic large cell lymphoma (ALCL) patients. To investigate the consequences of aberrant expression of this receptor on lymphocytes, we generated transgenic mice that express IL-22R1 on lymphocytes. The health of these animals progressively deteriorated at 8 to 12 weeks of age, as they displayed respiratory distress, rough coat and sluggish movement, and subsequent lethality due to multiorgan inflammation. The IL-22R1 transgenic animals developed neutrophilia that correlated with increased levels of circulating IL-17 and granulocyte colony-stimulating factor. In addition, these mice had increased serum IL-22 levels, suggesting that T cells expressing IL-22R1 generate IL-22 in a positive autoregulatory loop. As a result of the mouse model findings, we analyzed circulating cytokine levels in ALK(+)ALCL patients and detected elevated levels of IL-22, IL-17, and IL-8 in untreated patient samples. Importantly, IL-22 and IL-17 were undetectable in all patients who were in complete remission after chemotherapy. This study documents a previously unknown role of IL-22R1 in inflammation and identifies the involvement of IL-22R1/IL-22 in ALK(+)ALCL."xsd:string
http://purl.uniprot.org/citations/20971950http://purl.org/dc/terms/identifier"doi:10.1182/blood-2010-05-285908"xsd:string
http://purl.uniprot.org/citations/20971950http://purl.uniprot.org/core/author"Wilson W.H."xsd:string
http://purl.uniprot.org/citations/20971950http://purl.uniprot.org/core/author"Feigenbaum L."xsd:string
http://purl.uniprot.org/citations/20971950http://purl.uniprot.org/core/author"Anderson S.K."xsd:string
http://purl.uniprot.org/citations/20971950http://purl.uniprot.org/core/author"Pittaluga S."xsd:string
http://purl.uniprot.org/citations/20971950http://purl.uniprot.org/core/author"Ramakrishnan K."xsd:string
http://purl.uniprot.org/citations/20971950http://purl.uniprot.org/core/author"Young H.A."xsd:string
http://purl.uniprot.org/citations/20971950http://purl.uniprot.org/core/author"Donnelly R.P."xsd:string
http://purl.uniprot.org/citations/20971950http://purl.uniprot.org/core/author"Savan R."xsd:string
http://purl.uniprot.org/citations/20971950http://purl.uniprot.org/core/author"Klinman D.M."xsd:string
http://purl.uniprot.org/citations/20971950http://purl.uniprot.org/core/author"Shirota H."xsd:string
http://purl.uniprot.org/citations/20971950http://purl.uniprot.org/core/author"Reynolds D.A."xsd:string
http://purl.uniprot.org/citations/20971950http://purl.uniprot.org/core/author"Dunleavy K."xsd:string
http://purl.uniprot.org/citations/20971950http://purl.uniprot.org/core/author"Karwan M."xsd:string
http://purl.uniprot.org/citations/20971950http://purl.uniprot.org/core/author"McFarland A.P."xsd:string
http://purl.uniprot.org/citations/20971950http://purl.uniprot.org/core/date"2011"xsd:gYear
http://purl.uniprot.org/citations/20971950http://purl.uniprot.org/core/name"Blood"xsd:string
http://purl.uniprot.org/citations/20971950http://purl.uniprot.org/core/pages"575-584"xsd:string
http://purl.uniprot.org/citations/20971950http://purl.uniprot.org/core/title"A novel role for IL-22R1 as a driver of inflammation."xsd:string
http://purl.uniprot.org/citations/20971950http://purl.uniprot.org/core/volume"117"xsd:string
http://purl.uniprot.org/citations/20971950http://www.w3.org/2004/02/skos/core#exactMatchhttp://purl.uniprot.org/pubmed/20971950
http://purl.uniprot.org/citations/20971950http://xmlns.com/foaf/0.1/primaryTopicOfhttps://pubmed.ncbi.nlm.nih.gov/20971950
http://purl.uniprot.org/uniprot/#_A0A0U1RP02-mappedCitation-20971950http://www.w3.org/1999/02/22-rdf-syntax-ns#objecthttp://purl.uniprot.org/citations/20971950