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http://purl.uniprot.org/citations/30314757http://www.w3.org/1999/02/22-rdf-syntax-ns#typehttp://purl.uniprot.org/core/Journal_Citation
http://purl.uniprot.org/citations/30314757http://www.w3.org/2000/01/rdf-schema#comment"CD8+ T cell exhaustion impedes control of chronic viral infection; yet how new T cell responses are mounted during chronic infection is unclear. Unlike T cells primed at the onset of infection that rapidly differentiate into effectors and exhaust, we demonstrate that virus-specific CD8+ T cells primed after establishment of chronic LCMV infection preferentially generate memory-like transcription factor TCF1+ cells that were transcriptionally and proteomically distinct, less exhausted, and more responsive to immunotherapy. Mechanistically, adaptations of antigen-presenting cells and diminished T cell signaling intensity promoted differentiation of the memory-like subset at the expense of rapid effector cell differentiation, which was now highly dependent on IL-21-mediated CD4+ T cell help for its functional generation. Chronic viral infection similarly redirected de novo differentiation of tumor-specific CD8+ T cells, ultimately preventing cancer control. Thus, targeting these T cell stimulatory pathways could enable strategies to control chronic infection, tumors, and enhance immunotherapeutic efficacy."xsd:string
http://purl.uniprot.org/citations/30314757http://purl.org/dc/terms/identifier"doi:10.1016/j.immuni.2018.08.002"xsd:string
http://purl.uniprot.org/citations/30314757http://purl.uniprot.org/core/author"Law J.C."xsd:string
http://purl.uniprot.org/citations/30314757http://purl.uniprot.org/core/author"Brooks D.G."xsd:string
http://purl.uniprot.org/citations/30314757http://purl.uniprot.org/core/author"Guidos C.J."xsd:string
http://purl.uniprot.org/citations/30314757http://purl.uniprot.org/core/author"Gavin M.A."xsd:string
http://purl.uniprot.org/citations/30314757http://purl.uniprot.org/core/author"Dickson R.J."xsd:string
http://purl.uniprot.org/citations/30314757http://purl.uniprot.org/core/author"McGaha T.L."xsd:string
http://purl.uniprot.org/citations/30314757http://purl.uniprot.org/core/author"Snell L.M."xsd:string
http://purl.uniprot.org/citations/30314757http://purl.uniprot.org/core/author"Hezaveh K."xsd:string
http://purl.uniprot.org/citations/30314757http://purl.uniprot.org/core/author"Elsaesser H.J."xsd:string
http://purl.uniprot.org/citations/30314757http://purl.uniprot.org/core/author"Osokine I."xsd:string
http://purl.uniprot.org/citations/30314757http://purl.uniprot.org/core/author"MacLeod B.L."xsd:string
http://purl.uniprot.org/citations/30314757http://purl.uniprot.org/core/date"2018"xsd:gYear
http://purl.uniprot.org/citations/30314757http://purl.uniprot.org/core/name"Immunity"xsd:string
http://purl.uniprot.org/citations/30314757http://purl.uniprot.org/core/pages"678-694.e5"xsd:string
http://purl.uniprot.org/citations/30314757http://purl.uniprot.org/core/title"CD8+ T Cell Priming in Established Chronic Viral Infection Preferentially Directs Differentiation of Memory-like Cells for Sustained Immunity."xsd:string
http://purl.uniprot.org/citations/30314757http://purl.uniprot.org/core/volume"49"xsd:string
http://purl.uniprot.org/citations/30314757http://www.w3.org/2004/02/skos/core#exactMatchhttp://purl.uniprot.org/pubmed/30314757
http://purl.uniprot.org/citations/30314757http://xmlns.com/foaf/0.1/primaryTopicOfhttps://pubmed.ncbi.nlm.nih.gov/30314757
http://purl.uniprot.org/uniprot/#_P01887-mappedCitation-30314757http://www.w3.org/1999/02/22-rdf-syntax-ns#objecthttp://purl.uniprot.org/citations/30314757
http://purl.uniprot.org/uniprot/#_Q3U679-mappedCitation-30314757http://www.w3.org/1999/02/22-rdf-syntax-ns#objecthttp://purl.uniprot.org/citations/30314757
http://purl.uniprot.org/uniprot/#_Q9D239-mappedCitation-30314757http://www.w3.org/1999/02/22-rdf-syntax-ns#objecthttp://purl.uniprot.org/citations/30314757
http://purl.uniprot.org/uniprot/P01887http://purl.uniprot.org/core/mappedCitationhttp://purl.uniprot.org/citations/30314757