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http://purl.uniprot.org/citations/27799548http://www.w3.org/1999/02/22-rdf-syntax-ns#typehttp://purl.uniprot.org/core/Journal_Citation
http://purl.uniprot.org/citations/27799548http://www.w3.org/2000/01/rdf-schema#comment"The protein encoded by the autoimmune-associated protein tyrosine phosphatase nonreceptor type 22 gene, PTPN22, has wide-ranging effects in immune cells including suppression of T-cell receptor signaling and promoting efficient production of type I interferons (IFN-I) by myeloid cells. Here we show that mice deficient in PTPN22 resist chronic viral infection with lymphocytic choriomeningitis virus clone 13 (LCMV cl13). The numbers and function of viral-specific CD4 T lymphocytes is greatly enhanced, whereas expression of the IFNβ-induced IL-2 repressor, cAMP-responsive element modulator (CREM) is reduced. Reduction of CREM expression in wild-type CD4 T lymphocytes prevents the loss of IL-2 production by CD4 T lymphocytes during infection with LCMV cl13. These findings implicate the IFNβ/CREM/IL-2 axis in regulating T-lymphocyte function during chronic viral infection."xsd:string
http://purl.uniprot.org/citations/27799548http://purl.org/dc/terms/identifier"doi:10.1073/pnas.1603738113"xsd:string
http://purl.uniprot.org/citations/27799548http://purl.uniprot.org/core/author"Sherman L.A."xsd:string
http://purl.uniprot.org/citations/27799548http://purl.uniprot.org/core/author"Teijaro J.R."xsd:string
http://purl.uniprot.org/citations/27799548http://purl.uniprot.org/core/author"Marquardt K."xsd:string
http://purl.uniprot.org/citations/27799548http://purl.uniprot.org/core/author"Maine C.J."xsd:string
http://purl.uniprot.org/citations/27799548http://purl.uniprot.org/core/date"2016"xsd:gYear
http://purl.uniprot.org/citations/27799548http://purl.uniprot.org/core/name"Proc Natl Acad Sci U S A"xsd:string
http://purl.uniprot.org/citations/27799548http://purl.uniprot.org/core/pages"E7231-E7239"xsd:string
http://purl.uniprot.org/citations/27799548http://purl.uniprot.org/core/title"PTPN22 contributes to exhaustion of T lymphocytes during chronic viral infection."xsd:string
http://purl.uniprot.org/citations/27799548http://purl.uniprot.org/core/volume"113"xsd:string
http://purl.uniprot.org/citations/27799548http://www.w3.org/2004/02/skos/core#exactMatchhttp://purl.uniprot.org/pubmed/27799548
http://purl.uniprot.org/citations/27799548http://xmlns.com/foaf/0.1/primaryTopicOfhttps://pubmed.ncbi.nlm.nih.gov/27799548
http://purl.uniprot.org/uniprot/#_E9QAS3-mappedCitation-27799548http://www.w3.org/1999/02/22-rdf-syntax-ns#objecthttp://purl.uniprot.org/citations/27799548
http://purl.uniprot.org/uniprot/#_P29352-mappedCitation-27799548http://www.w3.org/1999/02/22-rdf-syntax-ns#objecthttp://purl.uniprot.org/citations/27799548
http://purl.uniprot.org/uniprot/#_Q3TEL9-mappedCitation-27799548http://www.w3.org/1999/02/22-rdf-syntax-ns#objecthttp://purl.uniprot.org/citations/27799548
http://purl.uniprot.org/uniprot/P29352http://purl.uniprot.org/core/mappedCitationhttp://purl.uniprot.org/citations/27799548
http://purl.uniprot.org/uniprot/E9QAS3http://purl.uniprot.org/core/mappedCitationhttp://purl.uniprot.org/citations/27799548
http://purl.uniprot.org/uniprot/Q3TEL9http://purl.uniprot.org/core/mappedCitationhttp://purl.uniprot.org/citations/27799548