Augmented production of soluble CD93 in patients with systemic sclerosis and clinical association with severity of skin sclerosis

Summary Background  The cell surface protein CD93, expressed on endothelial and myeloid cells, mediates phagocytosis, inflammation and cell adhesion. A soluble form of CD93 (sCD93) is released during inflammation. Objectives  To determine the serum sCD93 level and its association with clinical param...

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Veröffentlicht in:British journal of dermatology (1951) 2012-09, Vol.167 (3), p.542-547
Hauptverfasser: Yanaba, K., Asano, Y., Noda, S., Akamata, K., Aozasa, N., Taniguchi, T., Takahashi, T., Ichimura, Y., Toyama, T., Sumida, H., Kuwano, Y., Tada, Y., Sugaya, M., Kadono, T., Sato, S.
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Sprache:eng
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Zusammenfassung:Summary Background  The cell surface protein CD93, expressed on endothelial and myeloid cells, mediates phagocytosis, inflammation and cell adhesion. A soluble form of CD93 (sCD93) is released during inflammation. Objectives  To determine the serum sCD93 level and its association with clinical parameters in patients with systemic sclerosis (SSc). Methods  Serum sCD93 levels were examined by enzyme‐linked immunosorbent assay in 59 patients with SSc, 24 patients with systemic lupus erythematosus and 47 healthy individuals. The expression of CD93 in skin tissues was examined immunohistochemically. In a retrospective longitudinal study, sera from 11 patients with SSc were analysed. Results  Serum sCD93 levels were increased in patients with SSc compared with healthy individuals (P 
ISSN:0007-0963
1365-2133
DOI:10.1111/j.1365-2133.2012.11020.x