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特定神经肽在大疱性类天疱疮和疱疹样皮炎发病机制中的表达

Expression of selected neuropeptides in pathogenesis of bullous pemphigoid and dermatitis herpetiformis.

作者信息

Cynkier Anna, Zebrowska Agnieszka, Wągrowska-Danilewicz Małgorzata, Danilewicz Marian, Erkiert-Polguj Anna, Stasikowska-Kanicka Olga, Sysa-Jędrzejowska Anna, Waszczykowska Elżbieta

机构信息

Department of Dermatology and Venereology, Medical University of Lodz, Lodz, Poland.

出版信息

Pol J Pathol. 2012 Mar;63(1):31-9.

PMID:22535604
Abstract

Bullous pemphigoid (BP) and dermatitis herpetiformis (DH) are chronic subepidermal bullous diseases, which progress together with an itch and an inflammatory reaction. These symptoms may be the cause of a phenomenon described in the literature as a neurogenic skin inflammation. Neuropeptides are one of the mediators which take part in this process. The aim of our study was to indicate the expression of selected neuropeptides - CRF (corticotropin releasing factor), CGRP (calcitonin gene-related peptide), NKB (neurokinin B), SP (substance P) and the receptor for endothelin B (ETRB) - in the skin of patients suffering from BP or DH. A significantly increased expression of CRF was found in the specimen collected from the skin lesions of patients with BP and DH as well as a significantly increased expression of receptor for endothelin B in the patients with DH by the immunohistochemical method. The results obtained give evidence of a possible participation of CRF and receptor for endothelin B in the pathogenesis of the itch in the dermatitis herpetiformis as well as CRF in bullous pemphigoid.

摘要

大疱性类天疱疮(BP)和疱疹样皮炎(DH)是慢性表皮下大疱性疾病,伴有瘙痒和炎症反应。这些症状可能是文献中所描述的神经源性皮肤炎症现象的原因。神经肽是参与这一过程的介质之一。我们研究的目的是表明所选神经肽——促肾上腺皮质激素释放因子(CRF)、降钙素基因相关肽(CGRP)、神经激肽B(NKB)、P物质(SP)以及内皮素B受体(ETRB)——在BP或DH患者皮肤中的表达情况。通过免疫组织化学方法发现,从BP和DH患者皮肤病变处采集的标本中CRF表达显著增加,且DH患者中内皮素B受体的表达也显著增加。所获得的结果证明CRF和内皮素B受体可能参与疱疹样皮炎瘙痒的发病机制,以及CRF参与大疱性类天疱疮的发病机制。

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Expression of selected neuropeptides in pathogenesis of bullous pemphigoid and dermatitis herpetiformis.特定神经肽在大疱性类天疱疮和疱疹样皮炎发病机制中的表达
Pol J Pathol. 2012 Mar;63(1):31-9.
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