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肿瘤坏死因子-α诱导人类朗格汉斯细胞迁移。

Tumour necrosis factor-alpha induces Langerhans cell migration in humans.

作者信息

Cumberbatch M, Griffiths C E, Tucker S C, Dearman R J, Kimber I

机构信息

Zeneca Central Toxicology Laboratory, Alderley Park, Macclesfield, Cheshire SK10 4TJ, UK.

出版信息

Br J Dermatol. 1999 Aug;141(2):192-200. doi: 10.1046/j.1365-2133.1999.02964.x.

Abstract

The role of tumour necrosis factor (TNF)-alpha in the mobilization and migration of human epidermal Langerhans cells (LC) has been investigated. Intradermal injection of normal human volunteers with homologous recombinant TNF-alpha was found to cause a dose-dependent reduction in the frequency of LC within epidermal sheets 2 h later. Equivalent results were obtained when epidermal LC were identified on the basis of either CD1a or HLA-DR expression. At the dose of TNF-alpha used routinely (500 U), treatment resulted in an average reduction in LC density of approximately 24%. Treatment with TNF-alpha was associated with a perivascular polymorphonuclear infiltration at 2 h, but the epidermis appeared normal with neither fibrinoid necrosis nor vasculitis, and LC morphology was not affected significantly. These results demonstrate that TNF-alpha provides an important signal for LC migration in humans and is likely therefore to play a crucial part in the induction of cutaneous immune responses.

摘要

肿瘤坏死因子(TNF)-α在人表皮朗格汉斯细胞(LC)的动员和迁移中的作用已得到研究。向正常人类志愿者皮内注射同源重组TNF-α后发现,2小时后表皮片中LC的频率呈剂量依赖性降低。基于CD1a或HLA-DR表达鉴定表皮LC时,得到了相同的结果。在常规使用的TNF-α剂量(500 U)下,治疗导致LC密度平均降低约24%。TNF-α治疗在2小时时伴有血管周围多形核细胞浸润,但表皮外观正常,既无纤维蛋白样坏死也无血管炎,LC形态也未受到显著影响。这些结果表明,TNF-α为人类LC迁移提供了重要信号,因此可能在皮肤免疫反应的诱导中起关键作用。

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