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dc.contributor.authorShahneh, FZ
dc.contributor.authorMohammadian, M
dc.contributor.authorBabaloo, Z
dc.contributor.authorBaradaran, B
dc.date.accessioned2018-08-26T09:31:19Z
dc.date.available2018-08-26T09:31:19Z
dc.date.issued2013
dc.identifier.urihttp://dspace.tbzmed.ac.ir:8080/xmlui/handle/123456789/57001
dc.description.abstractBehط£آ§et Disease (BD) is an autoimmune disorder with recurrent ocular, vascular, central nervous system, articular, mucocutaneous, and gastrointestinal manifestations with unclear etiology and pathogenesis. The further characterization of inflammatory features of Behط£آ§et's disease may eventually lead to development of better treatment options. Clinical and laboratory observations suggested an important role of IL-17, IL-21 and neutrophil-mediated process in the pathogenesis of BD. New therapeutic modalities target specific and nonspecific suppression of the immune system. The various non-specific immunosuppressive drugs, used either alone or in combinations, frequently fail to control inflammation or maintain remissions. Due to encouraging clinical results (i.e. Antigenic specification, prolonged survival with acceptable levels of toxicity); antibody-based drugs could be effective for the clinical management of Behط£آ§et's disease. ط¢آ© 2013 by Tabriz University of Medical Sciences.
dc.language.isoEnglish
dc.relation.ispartofAdvanced Pharmaceutical Bulletin
dc.subjectadalimumab
dc.subjectcolchicine
dc.subjectetanercept
dc.subjectinfliximab
dc.subjectinterleukin 17
dc.subjectinterleukin 21
dc.subjectarticle
dc.subjectBehcet disease
dc.subjectcell activation
dc.subjectcytokine production
dc.subjectdisease association
dc.subjectdrug efficacy
dc.subjecthuman
dc.subjectimmunopathogenesis
dc.subjectimmunotherapy
dc.subjectinnate immunity
dc.subjectleukocyte activation
dc.subjectTh17 cell
dc.titleNew approaches in immunotherapy of behçet disease
dc.typeArticle
dc.citation.volume3
dc.citation.issue1
dc.citation.spage9
dc.citation.epage11
dc.citation.indexScopus
dc.identifier.DOIhttps://doi.org/10.5681/apb.2013.002


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