白癜风
脱色
FOXP3型
医学
免疫学
免疫染色
病理
分子生物学
免疫组织化学
免疫系统
生物
皮肤病科
作者
Marwa Abdallah,Ranya Lotfi,Wessam Othman,Riham Galal
摘要
Abstract Background The exact etiology of vitiligo remains obscure. Studies have indicated a role for cellular immunity in the pathogenesis of vitiligo. The aim of this study is to assess tissue F oxP3 + natural regulatory T ‐cells (Tregs), as well as CD 4 + and CD 8 + T‐cells in active vs. stable nonsegmental vitiligo. Materials and methods Immunohistochemical double‐staining for expression of CD 4 + and CD 8 + T ‐cells with immunostaining for expression of F oxP3 in lesional, marginal, and nonlesional skin of nonsegmental vitiligo was used to evaluate the abundance of Tregs among CD 4 + and CD 8 + T‐cells in active and stable cases of vitiligo. Results A significant increase in the number of CD 4 + and CD 8 + T‐cells and a highly significant reduction in the number of F oxP3‐expressing Tregs were detected in marginal skin in both stable and active vitiligo cases. F oxP3 + cells were decreased in tissue of patients with vitiligo compared with healthy controls. The number of CD 8 + T‐cells was increased in the epidermis and dermoepidermal junction ( DEJ ) in comparison with the number of CD 4 + T ‐cells. Tregs were mostly present at the DEJ . Conclusion The reduction in the number of FoxP3 + cells in the marginal skin suggests that this is the site where regulatory activity is needed to suppress the activity of helper and cytotoxic T‐cells that are actively contributing to depigmentation.
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