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Updated: Nov 4, 2025

Lymphocyte Isolation from Human Skin for Phenotypic Analysis and Ex Vivo Cell Culture
Published on: April 8, 2016
CD93 has a crucial role in pathogenesis of psoriasis
Wafaa Ahmed Shehata1, Alaa Hassan Maraee1, Nermin Tayel2
1Department of Dermatology, Andrology and STDs, Faculty of Medicine- Menoufia University, Shebin El-Kom, Egypt.
Insights
Cluster of differentiation 93 (CD93) is significantly expressed in psoriatic skin, indicating its role in disease pathogenesis. This finding suggests CD93 as a potential therapeutic target for psoriasis.
Area of Science:
- Dermatology and immunology
- Molecular biology and genetics
Background:
- Psoriasis is a chronic inflammatory skin condition characterized by epidermal proliferation and angiogenesis.
- Cluster of differentiation 93 (CD93) is an angiogenic factor involved in cell adhesion and inflammation.
Purpose of the Study:
- To investigate the immunohistochemical expression of CD93 in psoriatic skin.
- To examine the association between CD93 single nucleotide polymorphisms (SNPs) rs2749817 and psoriasis pathogenesis and severity.
Main Methods:
- A case-control study involving 50 psoriasis vulgaris patients and 50 healthy controls.
- Immunohistochemical staining of skin biopsies to assess CD93 expression.
- Real-time PCR (TaqMan assay) to analyze CD93 rs2749817 gene polymorphism.
Main Results:
- CD93 expression was significantly higher in dermal endothelial and inflammatory cells of psoriatic skin compared to controls.
- Stronger CD93 intensity and higher positive cell percentages were observed in psoriasis patients.
- The TC genotype of CD93 rs2749817 was less frequent in patients, while the CC genotype was exclusively found in cases.
Conclusions:
- Cluster of differentiation 93 (CD93) plays a significant role in the pathogenesis of psoriasis.
- CD93 represents a promising therapeutic target for managing psoriasis.
Background:
Psoriasis is a chronic, immune-related disorder; inflammation, higher rate of epidermal proliferation, and angiogenesis are the main pathognomonic features. Cluster of differentiation 93 (CD93), an angiogenic element, plays a role in cell adhesion regulation and has a putative function in inflammation.
Objective:
To assess CD93 immunohistochemical expression in psoriatic skin and the association of CD93 single nucleotide polymorphisms (SNPs) rs2749817 to disease pathogenesis and severity.
Methods:
This case-control study was done on 50 patients with psoriasis vulgaris beside 50 age- and sex-matched healthy controls. Assessment of psoriasis severity was done by Psoriasis Area and Severity Index (PASI) score. 3 mm punch skin biopsies were taken from every participant, and hematoxylin and eosin staining and immunohistochemical staining for CD93 antibody were done. Assessment of CD93 rs2749817 gene polymorphism by the TaqMan allelic discrimination assay technique (real-time PCR) was done.
Results:
Immunohistochemical expression of CD93 showed membrano-cytoplasmic localization in both endothelial and inflammatory cells of cases and controls with significant more positivity in dermal endothelial and inflammatory cells of cases than controls (p = 0.001 and 0.014 respectively). Strong intensity was present in 18 of cases endothelial cells and 24 inflammatory cells with absence in controls (p = 0.001 for both) with significantly higher H-score and higher percent of positive cells (p = 0.001 for both). The TC genotype was lower in patients compared to control (p-value = 0.006) and CC genotype which was present only in cases (p-value = 0.021).
Conclusion:
Cluster of differentiation 93 has an essential role in psoriasis and an encouraging future therapy for psoriasis.
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