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Psoriasis and Pro-angiogenetic Factor CD93: Gene Expression and Association with Gene Polymorphism Suggests a Role in
Albert Duvetorp1, Renate Slind Olsen, Marita Skarstedt
1Division of Dermatology, Ryhov Hospital, SE-55185 Jönköping, Sweden. albert.duvetorp@gmail.com.
Insights
CD93 protein is elevated in psoriasis skin, suggesting its role in the disease. Genetic variations in CD93 are linked to psoriasis, but narrowband UVB treatment doesn't affect its skin expression.
Area of Science:
- Immunology
- Dermatology
- Genetics
Background:
- Psoriasis pathogenesis involves angiogenesis and inflammation.
- CD93 (also known as C1qRp) is implicated in these processes.
Purpose of the Study:
- To investigate the role of CD93 in psoriasis.
- To assess CD93 expression and its association with genetic polymorphisms in patients with psoriasis.
Main Methods:
- Studied CD93 in serum, peripheral blood mononuclear cells, and skin of psoriasis patients and controls.
- Analyzed CD93 gene polymorphisms (rs2749812, rs2749817).
- Evaluated the effect of narrowband ultraviolet B (NB-UVB) treatment on CD93 skin expression.
Main Results:
- CD93 gene expression was significantly higher in lesional and non-lesional psoriatic skin.
- CD93 protein was detected in dermal endothelial cells of lesional skin.
- Psoriasis showed a significant association with the CD93 gene polymorphism rs2749817.
- NB-UVB treatment did not alter CD93 skin gene expression.
Conclusions:
- Increased CD93 expression in psoriatic skin and its association with the rs2749817 polymorphism suggest CD93 is involved in psoriasis pathogenesis.
- CD93 may represent a potential therapeutic target for psoriasis.
Abstract:
CD93 is involved in angiogenesis and inflammation, both of which are key processes in the pathogenesis of psoriasis. CD93 was studied in serum, peripheral blood mononuclear cells and skin of patients with psoriasis and controls. Furthermore, allele frequencies for CD93 single-nucleotide polymorphisms rs2749812 and rs2749817 were assessed in patients with psoriasis compared with controls and the effect of narrowband ultraviolet B (NB-UVB) treatment on CD93 gene expression was evaluated in the skin of patients with psoriasis. CD93 gene expression was significantly increased in lesional and non-lesional skin from patients with psoriasis compared with controls. Immunohistochemistry revealed CD93 staining in dermal endothelial cells in lesional skin, and psoriasis was significantly associated with rs2749817 CD93 gene polymorphism. NB-UVB treatment of patients with psoriasis did not alter skin CD93 gene expression. Increased protein expression of CD93 psoriatic skin and association with the rs2749817 polymorphism suggests that CD93 plays a role in psoriasis disease pathogenesis.
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