Publication:
The role of infectious agents in the pathogenesis, clinical manifestations and treatment strategies in Behcet's disease

dc.contributor.authorsMumcu, G.; Inanc, N.; Yavuz, S.; Direskeneli, H.
dc.date.accessioned2022-03-12T17:32:25Z
dc.date.accessioned2026-01-11T05:57:12Z
dc.date.available2022-03-12T17:32:25Z
dc.date.issued2007
dc.description.abstractBehcet's disease (BD) is a multisystemic disorder characterized by oral, genital ulcers and involvement of the cutaneous (erythema nodosum, pustular vasculitis), ocular (anterior or posterior uveitis), musculoskeletal, vascular (both arterial and venous vasculitis), gastrointestinal and central nervous (meningoencephalitis) systems. It has an unpredictable clinical spectrum from mild mucocutaneous manifestations to severe ocular, vascular or neurological disability. In this review, the aetiology, clinical presentations and treatment modalities of BD are evaluated in the context of microbial factors within the existing literature. The relationships between microbial agents (streptococcia and herpes simplex virus), microbial antigens [heat shock proteins (HSP), lipoteichoic acid (LTA)] and immune mechanisms such as innate and adaptive responses against microorganisms are discussed.
dc.identifier.doidoiWOS:000252147400007
dc.identifier.eissn1593-098X
dc.identifier.issn0392-856X
dc.identifier.pubmed17949548
dc.identifier.urihttps://hdl.handle.net/11424/228573
dc.identifier.wosWOS:000252147400007
dc.language.isoeng
dc.publisherCLINICAL & EXPER RHEUMATOLOGY
dc.relation.ispartofCLINICAL AND EXPERIMENTAL RHEUMATOLOGY
dc.rightsinfo:eu-repo/semantics/closedAccess
dc.subjectetiopathogenesis
dc.subjectimmune responses
dc.subjectBehcet's disease
dc.subjectT-CELL RESPONSES
dc.subjectHEAT-SHOCK PROTEINS
dc.subjectSTREPTOCOCCUS-SANGUIS
dc.subjectLIPOTEICHOIC ACID
dc.subjectSKIN-LESIONS
dc.subjectSYMPTOMS
dc.subjectPOLYMORPHISMS
dc.subjectASSOCIATION
dc.subjectGENE
dc.subjectANTIGEN
dc.titleThe role of infectious agents in the pathogenesis, clinical manifestations and treatment strategies in Behcet's disease
dc.typearticle
dspace.entity.typePublication
oaire.citation.endPageS33
oaire.citation.issue4
oaire.citation.startPageS27
oaire.citation.titleCLINICAL AND EXPERIMENTAL RHEUMATOLOGY
oaire.citation.volume25

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