Downregulation of the inhibitor of apoptosis protein survivin in keratinocytes and endothelial cells in psoriasis skin following infliximab therapy

Summary Background  Survivin, an inhibitor of apoptosis protein (IAP), has been implicated in endothelial cell stability, through inhibition of apoptosis and in cell proliferation. Objectives  To evaluate the effect of antitumour necrosis factor (TNF)‐α therapy on survivin expression in psoriasis sk...

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Veröffentlicht in:British journal of dermatology (1951) 2006-12, Vol.155 (6), p.1191-1196
Hauptverfasser: Markham, T., Mathews, C., Rogers, S., Mullan, R., Bresnihan, B., FitzGerald, O., Veale, D.J., Fearon, U.
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Sprache:eng
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Zusammenfassung:Summary Background  Survivin, an inhibitor of apoptosis protein (IAP), has been implicated in endothelial cell stability, through inhibition of apoptosis and in cell proliferation. Objectives  To evaluate the effect of antitumour necrosis factor (TNF)‐α therapy on survivin expression in psoriasis skin at 0, 2 and 12 weeks after infliximab therapy. Methods  Skin biopsies were obtained from 16 patients; 11 also had arthritis with active skin/joint disease. Clinical scores [Psoriasis Area and Severity Index (PASI), involved body surface area (BSA), Disease Activity Score (DAS28) and Health Assessment Questionnaire] were recorded. Inflammatory infiltration and survivin protein expression were examined and graded by immunohistochemical staining, and mRNA levels were determined by real‐time polymerase chain reaction. Results  Survivin mRNA and protein were demonstrated in all baseline lesional biopsies. Survivin mRNA and protein expression was significantly greater in lesional compared with nonlesional baseline skin (P 
ISSN:0007-0963
1365-2133
DOI:10.1111/j.1365-2133.2006.07522.x