Suppr超能文献

人类免疫缺陷病毒调节蛋白tat、nef和rev的表位在特应性皮炎患者的皮肤中表达。

Epitopes of human immunodeficiency virus regulatory proteins tat, nef and rev are expressed in skin in atopic dermatitis.

作者信息

Schuurman H J, Joling P, van Wichen D F, Tobin D, van der Putte S C

机构信息

Department of Pathology, University Hospital, Utrecht, The Netherlands.

出版信息

Int Arch Allergy Immunol. 1993;100(2):107-14. doi: 10.1159/000236396.

Abstract

We extend our previous documentation that epitopes of HIV regulatory proteins tat, rev, and nef are expressed in tissue from uninfected individuals by the immunohistochemical analysis of normal skin (n = 10) and skin in some selected inflammatory dermatoses including urticaria (n = 6), systemic lupus erythematosus (n = 6), and atopic dermatitis (affected skin, n = 10, and after epicutaneous patch test for allergens, n = 8). A rabbit antibody to HIV-2 tat did not show immunolabeling of skin. Blood vessel endothelium was immunolabeled by one of two antibodies applied to HIV-1 tat, by an antibody to HIV-1 rev, and by two antibodies to HIV-1 nef. In addition one of the anti-nef antibodies labeled Langerhans cells. The anti-rev antibody labeled Langerhans cells and melanocytes in the epidermis, and dendritic cells in the dermis. The labeling of these skin components did not differ in prevalence between controls and groups of dermatosis. For other components, diseased skin conditions especially atopic dermatitis showed additional labeling. In affected skin, keratinocytes were labeled by antibodies to rev and one of two antibodies to nef. Skin after epicutaneous allergen patch testing also showed a statistically significantly increased prevalence of immunolabeling of dendritic cells and Langerhans cells by one of the anti-tat antibodies. We conclude that skin components show expression of epitopes recognized by antibodies to HIV-1 tat, rev, and nef; this expression is more extensive in atopic dermatitis than in normal skin, and can be further increased after epicutaneous allergen patch testing.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

我们扩展了之前的文献记录,通过对正常皮肤(n = 10)以及一些选定的炎症性皮肤病(包括荨麻疹,n = 6;系统性红斑狼疮,n = 6;特应性皮炎,患病皮肤,n = 10,以及在进行变应原经皮斑贴试验后,n = 8)的免疫组织化学分析,发现未感染个体的组织中表达了HIV调节蛋白tat、rev和nef的表位。一种针对HIV - 2 tat的兔抗体未显示皮肤的免疫标记。应用于HIV - 1 tat的两种抗体之一、针对HIV - 1 rev的抗体以及针对HIV - 1 nef的两种抗体对血管内皮进行了免疫标记。此外,一种抗nef抗体标记了朗格汉斯细胞。抗rev抗体标记了表皮中的朗格汉斯细胞和黑素细胞以及真皮中的树突状细胞。这些皮肤成分的标记在对照组和皮肤病组之间的发生率没有差异。对于其他成分,患病皮肤状况尤其是特应性皮炎显示出额外的标记。在患病皮肤中,角质形成细胞被针对rev的抗体以及针对nef的两种抗体之一标记。经皮变应原斑贴试验后的皮肤也显示,一种抗tat抗体对树突状细胞和朗格汉斯细胞的免疫标记发生率在统计学上显著增加。我们得出结论,皮肤成分显示出被针对HIV - 1 tat、rev和nef的抗体识别的表位的表达;这种表达在特应性皮炎中比在正常皮肤中更广泛,并且在经皮变应原斑贴试验后可以进一步增加。(摘要截短于250字)

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验