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迈向对麻风结节性红斑病理学的理解。

Towards understanding the pathology of erythema nodosum leprosum.

作者信息

Kahawita I P, Lockwood D N J

机构信息

Department of Infectious and Tropical Diseases, London School of Hygiene and Tropical Medicine, Keppel Street, London WC1E 7HT, UK.

出版信息

Trans R Soc Trop Med Hyg. 2008 Apr;102(4):329-37. doi: 10.1016/j.trstmh.2008.01.004. Epub 2008 Mar 3.

Abstract

Erythema nodosum leprosum (ENL) is an immune-mediated complication of leprosy presenting with inflammatory skin nodules and involvement of multiple organ systems, often running a protracted course. Immune complex production and deposition as well as complement activation have long been regarded as the principal aetiology of ENL. However, new data show that cell-mediated immunity is also important. We have performed a critical analysis of studies on the pathology of ENL. Our main findings are as follows. ENL is characterised by an inflammatory infiltrate of neutrophils with vasculitis and/or panniculitis. There is deposition of immune complexes and complement together with Mycobacterium leprae antigens in the skin. Changes in serum levels of Igs indicate a transient, localised immune response. The major T-cell subtype in ENL is the CD4 cell, in contrast to lepromatous leprosy where CD8 cells predominate. The cytokines TNFalpha and IL-6 are consistently found whilst IL-4 is low or absent in ENL lesions, indicating a T(H)1 type response. Keratinocyte 1a and intercellular adhesion molecule-1 (ICAM-1) have been shown to be present in the epidermis in ENL, which is evidence of a cell-mediated immune response. Co-stimulatory molecules such as B7-1 have also been studied but further work is needed to draw strong conclusions. We also highlight potential areas for future research.

摘要

结节性红斑麻风(ENL)是麻风的一种免疫介导并发症,表现为炎症性皮肤结节并累及多个器官系统,病程往往迁延。免疫复合物的产生和沉积以及补体激活长期以来一直被视为ENL的主要病因。然而,新数据表明细胞介导的免疫也很重要。我们对ENL的病理学研究进行了批判性分析。我们的主要发现如下。ENL的特征是伴有血管炎和/或脂膜炎的中性粒细胞炎性浸润。皮肤中有免疫复合物、补体以及麻风杆菌抗原的沉积。血清免疫球蛋白水平的变化表明存在短暂的局部免疫反应。与以CD8细胞为主的瘤型麻风不同,ENL中的主要T细胞亚型是CD4细胞。在ENL病变中始终能检测到细胞因子肿瘤坏死因子α(TNFα)和白细胞介素6(IL-6),而IL-4水平较低或不存在,表明是T(H)1型反应。已证实在ENL的表皮中有角蛋白1a和细胞间黏附分子-1(ICAM-1),这是细胞介导免疫反应的证据。也对共刺激分子如B7-1进行了研究,但需要进一步开展工作才能得出有力结论。我们还强调了未来研究的潜在领域。

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