Publication:
Monocyte activity in Behcet's disease

dc.contributor.authorsSahin, S; Lawrence, R; Direskeneli, H; Hamuryudan, V; Yazici, H; Akoglu, T
dc.date.accessioned2022-03-12T16:57:15Z
dc.date.accessioned2026-01-11T19:21:55Z
dc.date.available2022-03-12T16:57:15Z
dc.date.issued1996
dc.description.abstractMonocytes obtained from patients with Behcet's disease (BD) were examined for differentiation markers (expression of CD14 and antigens reacting with monoclonal antibodies 25F9 and G16/1) and for expression of selected adhesion molecules. There was significantly raised expression of the CD14 molecule, and increased staining with 25F9 and G16/1 antibodies in monocytes obtained from patients with ED. A monocyte activation marker, soluble CD14, was also found to be raised in patients' serum compared with normal serum (8.1 +/- 9.2 vs 1.4 +/- 0.7 mu g/ml). Furthermore, BD patients' monocyte culture supernatants caused significantly increased adhesion of normal neutrophils to endothelial cell monolayers in vitro. All these findings show that BD patients' monocytes are active in vivo and produce a number of pro-inflammatory cytokines which may play a role in the chronic inflammation found in these patients.
dc.identifier.doidoiWOS:A1996UM86300005
dc.identifier.issn0263-7103
dc.identifier.pubmed8646431
dc.identifier.urihttps://hdl.handle.net/11424/226906
dc.identifier.wosWOS:A1996UM86300005
dc.language.isoeng
dc.publisherOXFORD UNIV PRESS
dc.relation.ispartofBRITISH JOURNAL OF RHEUMATOLOGY
dc.rightsinfo:eu-repo/semantics/closedAccess
dc.subjectmonocyte
dc.subjectBehcet's disease
dc.subjectadhesion molecules
dc.subjectNECROSIS-FACTOR-ALPHA
dc.subjectHUMAN ENDOTHELIAL-CELLS
dc.subjectMACROPHAGES
dc.subjectCD14
dc.subjectLIPOPOLYSACCHARIDE
dc.subjectGENERATION
dc.subjectACTIVATION
dc.subjectADHERENCE
dc.subjectRECEPTOR
dc.subjectADHESION
dc.titleMonocyte activity in Behcet's disease
dc.typearticle
dspace.entity.typePublication
oaire.citation.endPage429
oaire.citation.issue5
oaire.citation.startPage424
oaire.citation.titleBRITISH JOURNAL OF RHEUMATOLOGY
oaire.citation.volume35

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