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利用人细胞系THP-1上的表面标志物CD86和/或CD54表达预测防腐剂致敏潜力。

Prediction of preservative sensitization potential using surface marker CD86 and/or CD54 expression on human cell line, THP-1.

作者信息

Sakaguchi Hitoshi, Miyazawa Masaaki, Yoshida Yukiko, Ito Yuichi, Suzuki Hiroyuki

机构信息

Kao Corporation, Safety and Microbial Control Research Center, 2606 Akabane, Ichikai-Machi, Haga-Gun, Tochigi, 321-3497, Japan.

出版信息

Arch Dermatol Res. 2007 Feb;298(9):427-37. doi: 10.1007/s00403-006-0714-9. Epub 2006 Nov 21.

Abstract

Preservatives are important components in many products, but have a history of purported allergy. Several assays [e.g., guinea pig maximization test (GPMT), local lymph node assay (LLNA)] are used to evaluate allergy potential of preservatives. We recently developed the human Cell Line Activation Test (h-CLAT), an in vitro skin sensitization test using human THP-1 cells. This test evaluates the augmentation of CD86 and CD54 expression, which are key events in the sensitization process, as an indicator of allergy following treatment with test chemical. Earlier, we found that a sub-toxic concentration was needed for the up-regulation of surface marker expression. In this study, we further evaluate the capability of h-CLAT to predict allergy potential using eight preservatives. Cytotoxicity was determined using propidium iodide with flow cytometry analysis and five doses that produce a 95, 85, 75, 65, and 50% cell viability were selected. If a material did not have any cytotoxicity at the highest technical dose (HTD), five doses are set using serial 1.3 dilutions of the HTD. The test materials used were six known allergic preservatives (e.g., methylchloroisothiazolinone/methylisothiazolinone, formaldehyde), and two non-allergic preservatives (methylparaben and 4-hydroxybenzoic acid). All allergic preservatives augmented CD86 and/or CD54 expression, indicating h-CLAT correctly identified the allergens. No augmentation was observed with the non-allergic preservatives; also correctly identified by h-CLAT. In addition, we report two threshold concentrations that may be used to categorize skin sensitization potency like the LLNA estimated concentration that yield a three-fold stimulation (EC3) value. These corresponding values are the estimated concentration which gives a relative fluorescence intensity (RFI) = 150 for CD86 and an RFI = 200 for CD54. These data suggest that h-CLAT, using THP-1 cells, may be able to predict the allergy potential of preservatives and possibility classify the potency of an allergen.

摘要

防腐剂是许多产品中的重要成分,但素有引发过敏的历史。有几种试验方法[如豚鼠最大化试验(GPMT)、局部淋巴结试验(LLNA)]用于评估防腐剂的过敏可能性。我们最近开发了人细胞系激活试验(h-CLAT),这是一种使用人THP-1细胞的体外皮肤致敏试验。该试验评估CD86和CD54表达的增加,这是致敏过程中的关键事件,作为受试化学品处理后过敏的指标。此前,我们发现上调表面标志物表达需要亚毒性浓度。在本研究中,我们使用八种防腐剂进一步评估h-CLAT预测过敏可能性的能力。使用碘化丙啶通过流式细胞术分析确定细胞毒性,并选择产生95%、85%、75%、65%和50%细胞活力的五个剂量。如果一种物质在最高技术剂量(HTD)下没有任何细胞毒性,则使用HTD的连续1.3倍稀释设置五个剂量。所用的受试材料为六种已知的过敏性防腐剂(如甲基氯异噻唑啉酮/甲基异噻唑啉酮、甲醛)和两种非过敏性防腐剂(对羟基苯甲酸甲酯和4-羟基苯甲酸)。所有过敏性防腐剂均增加了CD86和/或CD54的表达,表明h-CLAT正确识别了过敏原。非过敏性防腐剂未观察到增加;h-CLAT也正确识别。此外,我们报告了两个阈值浓度,可用于对皮肤致敏效力进行分类,类似于LLNA估计浓度产生三倍刺激(EC3)值。这些相应的值是使CD86的相对荧光强度(RFI)=150和CD54的RFI=200的估计浓度。这些数据表明,使用THP-1细胞的h-CLAT可能能够预测防腐剂的过敏可能性,并有可能对过敏原的效力进行分类。

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