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Updated: Jul 13, 2026

Human Neutrophil Flow Chamber Adhesion Assay
Published on: July 2, 2014
Pathogenesis-related adhesion molecules in Henoch-Schonlein vasculitis
Faysal Gok1, Yesim Ugur, Seza Ozen
1Department of Pediatric Nephrology, Gulhane Military Medical Academy, School of Medicine, 06018, Etlik, Ankara, Turkey. faysalgok@yahoo.com
Henoch-Schonlein purpura involves increased skin expression of adhesion molecules like P-selectin and ICAM-2 during the acute phase. These markers, crucial for inflammation, decrease as the condition resolves.
Area of Science:
- Immunology
- Dermatology
- Pathology
Background:
- Henoch-Schonlein purpura (HSP) is a systemic vasculitis characterized by inflammation.
- Adhesion molecules play a critical role in inflammatory cell recruitment and endothelial activation.
Purpose of the Study:
- To investigate the expression patterns of key adhesion molecules in HSP skin lesions.
- To compare the distribution of inflammation and endothelium-related adhesion molecules between acute and convalescent phases of HSP.
Main Methods:
- Skin biopsies were analyzed from pediatric patients with HSP during the acute purpura and convalescent phases.
- Immunohistochemical methods were used to assess the expression of P-selectin, E-selectin, ICAM-1, ICAM-2, ICAM-3, and VCAM-1.
Main Results:
- Significantly higher endothelial P-selectin, endothelial and inflammatory ICAM-2, and inflammatory ICAM-3 expression were observed in the acute phase compared to the convalescent phase.
- While decreased in the convalescent phase, the reduction in endothelial E-selectin, VCAM-1, and ICAM-1 expression was not statistically significant.
Conclusions:
- Specific adhesion molecules (P-selectin, ICAM-2, ICAM-3) are upregulated during the active phase of Henoch-Schonlein purpura.
- These findings highlight the role of endothelial activation and inflammatory cell infiltration in HSP pathogenesis.
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