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HIV疾病进展会影响表皮朗格汉斯细胞密度吗?

Does HIV disease progression influence epidermal Langerhans cell density?

作者信息

Nandwani R, Gazzard B G, Barton S E, Hawkins D A, Zemelman V, Staughton R C

机构信息

Department of HIV/Genitourinary Medicine, Chelsea & Westminster Hospital, London, U.K.

出版信息

Br J Dermatol. 1996 Jun;134(6):1087-92.

PMID:8763430
Abstract

Langerhans cells (LC) are antigen-presenting CD4+ dendritic cells in the skin which may become infected by the human immunodeficiency virus (HIV). Decreased LC function could account for the cutaneous manifestations seen in HIV disease. Previous studies of epidermal LC density in HIV-infected subjects have produced conflicting results. A definitive, prospective, case-control study was performed to determine whether there is an association between epidermal LC density and HIV clinical disease stage. Skin cryosections were stained with the CD1 monoclonal antibody using a three-step immunoperoxidase method. LC were counted by light microscopy and epidermal dimensions calculated with computer-assisted planimetry. The stage of the HIV clinical disease correlated with epidermal LC densities was quantified by three different methods: mean LC numbers per mm length of basement membrane, mean LC per mm2 of epidermal area, and mean LC population per mm of epidermal surface length. Seventy-one subjects, recruited from a large out-patient HIV clinic in London, comprised 56 HIV-positive men and 15 male HIV-negative controls. Contrary to previous smaller studies, there was no detectable association between epidermal LC density (quantified by any of the three methods) and the stage of the HIV clinical disease. Given that HIV infects large numbers of CD4+ cells, we propose possible hypotheses to account for the apparent preservation of static LC numbers in the skin. Further studies of LC kinetics and function are required to elucidate their role in the natural history of HIV infection.

摘要

朗格汉斯细胞(LC)是皮肤中呈递抗原的CD4⁺树突状细胞,可能会被人类免疫缺陷病毒(HIV)感染。LC功能下降可能是HIV疾病中出现皮肤表现的原因。先前关于HIV感染受试者表皮LC密度的研究结果相互矛盾。本研究进行了一项权威性的前瞻性病例对照研究,以确定表皮LC密度与HIV临床疾病分期之间是否存在关联。采用三步免疫过氧化物酶法,用CD1单克隆抗体对皮肤冷冻切片进行染色。通过光学显微镜计数LC,并使用计算机辅助平面测量法计算表皮尺寸。采用三种不同方法对与表皮LC密度相关的HIV临床疾病分期进行量化:每毫米基底膜长度的平均LC数量、每平方毫米表皮面积的平均LC数量以及每毫米表皮表面长度的平均LC总数。从伦敦一家大型门诊HIV诊所招募的71名受试者包括56名HIV阳性男性和15名HIV阴性男性对照。与先前规模较小的研究相反,表皮LC密度(通过三种方法中的任何一种进行量化)与HIV临床疾病分期之间未发现可检测到的关联。鉴于HIV感染大量CD4⁺细胞,我们提出了一些可能的假说来解释皮肤中静态LC数量明显保持不变的现象。需要进一步研究LC的动力学和功能,以阐明它们在HIV感染自然史中的作用。

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