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变应原特异性白细胞黏附抑制(LAI)试验:敏感性、特异性及机制

Allergen-specific leukocyte adherence inhibition (LAI) assay: sensitivity, specificity and mechanism.

作者信息

Fink A, Heller L, Eliraz A, Weisman Z, Miskin A, Schlezinger M, Bibi H, Bentwich Z

机构信息

Ruth Ben-Ari Institute of Clinical Immunology, Kaplan Hospital, Rehovot Israel.

出版信息

Immunol Lett. 1987 Oct;16(1):65-70. doi: 10.1016/0165-2478(87)90063-0.

Abstract

An allergen-specific tube leukocyte adherence inhibition (LAI) assay has been developed in order to study the mechanism by which leukocytes lose their normal property of adherence to glass. Peripheral blood leukocytes (PBL) from 27 individuals allergic to Dermatophagoides farinae (DF), 10 with seasonal rhinitis not induced by DF and 49 non-allergic healthy volunteers were challenged in vitro with DF and a non-relevant allergen, Artemisia vulgaris (AV) and then assayed for the ability to adhere to glass tubes. Challenge by DF, but not by AV, resulted in loss of adherence by PBL from patients allergic to DF, but not in those of normal controls. The specific LAI response was dose-dependent and occurred only when a critical dose of 0.5 X 10(3) was employed. Following in vitro challenge with DF, radio-immunoassay using an antiserum to LTC4 detected immunoreactive material in supernatants of PBL from DF-allergic individuals. When highly enriched mononuclear cells from non-allergic individuals were armed with cytophilic allergen-specific IgE and challenged with the specific allergen, they lost the property of glass adherence and released a substance that was immunoreactive with LTC4. The results suggest that the chain of events leading to the LAI response in PBL from allergic individuals involves primary recognition of the allergen by specific IgE antibodies bound to receptors on mononuclear cells. The cells are thus triggered to synthesize cysteinyl-containing leukotrienes which mediate the LAI phenomenon. The results suggest that this assay may be used to study allergen-antibody interaction and the subsequent events leading to the clinical picture of atopic diseases.

摘要

为了研究白细胞丧失其正常玻璃黏附特性的机制,已经开发出一种变应原特异性的试管白细胞黏附抑制(LAI)试验。用粉尘螨(DF)和一种不相关的变应原黄花蒿(AV)对27名对粉尘螨过敏的个体、10名非由粉尘螨诱发季节性鼻炎的个体以及49名非过敏健康志愿者的外周血白细胞(PBL)进行体外激发,然后检测其黏附于玻璃试管的能力。粉尘螨激发而非黄花蒿激发导致对粉尘螨过敏患者的PBL丧失黏附性,但正常对照组的PBL则未出现这种情况。特异性LAI反应呈剂量依赖性,且仅在使用0.5×10³的临界剂量时才会发生。用粉尘螨进行体外激发后,使用抗白三烯C4(LTC4)抗血清的放射免疫测定法在对粉尘螨过敏个体的PBL上清液中检测到免疫反应性物质。当用亲细胞性变应原特异性IgE武装非过敏个体的高度富集单核细胞并用特异性变应原进行激发时,它们丧失了玻璃黏附特性并释放出一种与LTC4有免疫反应性的物质。结果表明,导致过敏个体PBL中LAI反应的一系列事件涉及与单核细胞上受体结合的特异性IgE抗体对变应原的初次识别。这些细胞因此被触发合成含半胱氨酰的白三烯,后者介导LAI现象。结果表明,该试验可用于研究变应原 - 抗体相互作用以及导致特应性疾病临床表现的后续事件。

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