Expression and activity of IL-17 receptor subunits in human cutaneous cells as targets for anti-IL-17 therapeutic antibodies

被引:0
|
作者
Wohlrab, Johannes [1 ,2 ]
Gerloff, Dennis [1 ]
Gebhardt, Kathleen [1 ]
机构
[1] Martin Luther Univ Halle Wittenberg, Dept Dermatol & Venerol, Ernst Grube Str 40, D-06097 Halle, Germany
[2] Martin Luther Univ Halle Wittenberg, Inst Appl Dermatopharm, Halle, Germany
关键词
Psoriatic pathogenesis; IL-17; cytokines; receptors; ENDOTHELIAL-CELLS; T(H)17 CELLS; PSORIASIS; SKIN; KERATINOCYTES; COMORBIDITY; CYTOKINE; PROLIFERATION; PHENOTYPE; PROMOTES;
D O I
10.1016/j.biopha.2021.112569
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
The key players in different chronic inflammatory skin diseases are cytokines belonging to the IL-17 group, IL-17 receptors and a T helper cell population, Th17 cells. Successful therapeutic strategies that target either IL-17 or the major IL-17 receptor IL-17RA have confirmed the immune-pathogenic pathway. To study the IL-17-ligand receptor axis at the molecular level, a number of cutaneous cell types from healthy human subjects has been cultured and analyzed for the expression of IL-17 receptors. IL-17RA was the most abundantly expressed receptor type in keratinocytes, epidermal stem cells, fibroblasts, mesenchymal stem cells, hemo- and lymphovascular endothelial cells. IL-17RC and IL-17RD showed moderate expression, while the genes for IL-17RB and IL-17RE were poorly expressed. In none of the investigated cell types, IL-17 ligands caused an increased expression level of the five receptor types in time- and dose-dependent experiments. No evidence for IL-17A, -C, -E or -F induced signal transduction cascades could be obtained by a qRT-PCR and western blot analyses. Further studies are necessary to identify relevant co-stimulating factors from IL-17 subtypes under physiological and pathophysiological conditions.
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页数:8
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