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http://purl.uniprot.org/citations/27033173http://www.w3.org/1999/02/22-rdf-syntax-ns#typehttp://purl.uniprot.org/core/Journal_Citation
http://purl.uniprot.org/citations/27033173http://www.w3.org/2000/01/rdf-schema#comment"Multiple sclerosis (MS) is considered as a T cell mediated autoimmune disease of the CNS, although a pathogenic role has also been attributed to other immune cell types as well as to environmental and genetic factors. Considering that T cells are interesting from an immunopathogenic point of view and consequently from a therapeutic perspective, various T cell targeted therapies have been approved for MS. Interferon beta (IFN-β) is widely used as first-line intervention for modulating T cell responses, although its pleiotropic and multifaceted activities influence its effectiveness on the disease development, with mechanisms that are not yet fully understood. Since different T cell populations, including pro-inflammatory and regulatory T cells, might affect the course of MS, the effects of IFN-β become even more complex. This review will summarize recent findings regarding the T cell targeted effect of IFN-β in MS and its animal model EAE, with emphasis on the direct actions of endogenous and exogenous IFN-β on each T cell subpopulation involved in CNS autoimmunity. Delineating how IFN-β exerts its action on different T cell types may eventually contribute to the designing of therapeutic strategies aiming to improve the effectiveness of this drug for MS treatment."xsd:string
http://purl.uniprot.org/citations/27033173http://purl.org/dc/terms/identifier"doi:10.1016/j.cytogfr.2016.03.013"xsd:string
http://purl.uniprot.org/citations/27033173http://purl.uniprot.org/core/author"Haralambous S."xsd:string
http://purl.uniprot.org/citations/27033173http://purl.uniprot.org/core/author"Kavrochorianou N."xsd:string
http://purl.uniprot.org/citations/27033173http://purl.uniprot.org/core/author"Markogiannaki M."xsd:string
http://purl.uniprot.org/citations/27033173http://purl.uniprot.org/core/date"2016"xsd:gYear
http://purl.uniprot.org/citations/27033173http://purl.uniprot.org/core/name"Cytokine Growth Factor Rev"xsd:string
http://purl.uniprot.org/citations/27033173http://purl.uniprot.org/core/pages"47-54"xsd:string
http://purl.uniprot.org/citations/27033173http://purl.uniprot.org/core/title"IFN-beta differentially regulates the function of T cell subsets in MS and EAE."xsd:string
http://purl.uniprot.org/citations/27033173http://purl.uniprot.org/core/volume"30"xsd:string
http://purl.uniprot.org/citations/27033173http://www.w3.org/2004/02/skos/core#exactMatchhttp://purl.uniprot.org/pubmed/27033173
http://purl.uniprot.org/citations/27033173http://xmlns.com/foaf/0.1/primaryTopicOfhttps://pubmed.ncbi.nlm.nih.gov/27033173
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http://purl.uniprot.org/uniprot/#_B5BUQ5-mappedCitation-27033173http://www.w3.org/1999/02/22-rdf-syntax-ns#objecthttp://purl.uniprot.org/citations/27033173
http://purl.uniprot.org/uniprot/#_P01574-mappedCitation-27033173http://www.w3.org/1999/02/22-rdf-syntax-ns#objecthttp://purl.uniprot.org/citations/27033173
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http://purl.uniprot.org/uniprot/#_Q15943-mappedCitation-27033173http://www.w3.org/1999/02/22-rdf-syntax-ns#objecthttp://purl.uniprot.org/citations/27033173
http://purl.uniprot.org/uniprot/A0A7R8GV38http://purl.uniprot.org/core/mappedCitationhttp://purl.uniprot.org/citations/27033173
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http://purl.uniprot.org/uniprot/B5BUQ5http://purl.uniprot.org/core/mappedCitationhttp://purl.uniprot.org/citations/27033173