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肿瘤坏死因子α定位于鼻黏膜肥大细胞,并在急性变应性鼻炎中释放。

TNF alpha is localized to nasal mucosal mast cells and is released in acute allergic rhinitis.

作者信息

Bradding P, Mediwake R, Feather I H, Madden J, Church M K, Holgate S T, Howarth P H

机构信息

Immunopharmacology Group, Southampton University, UK.

出版信息

Clin Exp Allergy. 1995 May;25(5):406-15. doi: 10.1111/j.1365-2222.1995.tb01071.x.

DOI:10.1111/j.1365-2222.1995.tb01071.x
PMID:7553243
Abstract

Allergic mucosal inflammation is characterized by tissue infiltration with eosinophils, and associated activation of mast cells and T lymphocytes. Tumour necrosis factor (TNF) alpha/cachectin is a candidate cytokine relevant to the pathogenesis of these events through its capacity to upregulate the expression of endothelial cell adhesion molecules, mediate granulocyte chemoattraction, and activate eosinophils, mast cells and T cells. To investigate the presence and localization of TNF alpha in the nasal mucosa in allergic rhinitis, nasal biopsies from perennial rhinitic (n = 13) and non-rhinitic volunteers (n = 11) were embedded in glycol methacrylate and immunostained with a monoclonal antibody directed against TNF alpha, and adjacent 2 microns sections stained for tryptase, CD3 and eosinophil cationic protein. This identified positive immunostaining for TNF alpha in the submucosa of both the rhinitic and normal subjects (median cell counts 13 and 23 cells/mm2 respectively, P = 0.24) with cellular localization to mast cells but not to T-lymphocytes or eosinophils. In a subsequent study of seven atopic subjects, nasal allergen challenge produced increases in lavage levels of histamine and albumin, which was associated with significant release of TNF alpha as early as 2 min post-allergen when compared with the saline control day (P = 0.05). This difference was also apparent when studying the area under the curve both at 30 and 60 min post-challenge t-test (P = 0.015 and 0.02 respectively).(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

变应性黏膜炎症的特征是嗜酸性粒细胞浸润组织,并伴有肥大细胞和T淋巴细胞的激活。肿瘤坏死因子(TNF)α/恶病质素是一种候选细胞因子,通过上调内皮细胞黏附分子的表达、介导粒细胞趋化作用以及激活嗜酸性粒细胞、肥大细胞和T细胞,与这些事件的发病机制相关。为了研究变应性鼻炎患者鼻黏膜中TNFα的存在和定位,将常年性鼻炎患者(n = 13)和非鼻炎志愿者(n = 11)的鼻活检组织包埋在甲基丙烯酸乙二醇酯中,并用抗TNFα单克隆抗体进行免疫染色,相邻的2微米切片用嗜酸性粒细胞阳离子蛋白、CD3和类胰蛋白酶染色。结果发现,鼻炎患者和正常受试者的黏膜下层均有TNFα阳性免疫染色(中位数细胞计数分别为13和23个细胞/mm²,P = 0.24),细胞定位于肥大细胞,而非T淋巴细胞或嗜酸性粒细胞。在随后对7名特应性受试者的研究中,鼻内变应原激发导致灌洗液中组胺和白蛋白水平升高,与生理盐水对照日相比,变应原激发后2分钟TNFα即显著释放(P = 0.05)。在研究激发后30分钟和60分钟的曲线下面积时,这种差异也很明显(t检验,P分别为0.015和0.02)。(摘要截短至250字)

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