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基于体外多试验数据的人工神经网络分析用于预测化学品的皮肤致敏强度。

Artificial neural network analysis of data from multiple in vitro assays for prediction of skin sensitization potency of chemicals.

机构信息

Shiseido Research Center, Shiseido Co Ltd, 2-12-1 Fukuura, Kanazawa-ku, Yokohama-shi, Kanagawa 236-8643, Japan.

出版信息

Toxicol In Vitro. 2013 Jun;27(4):1233-46. doi: 10.1016/j.tiv.2013.02.013. Epub 2013 Mar 1.

DOI:10.1016/j.tiv.2013.02.013
PMID:23458967
Abstract

In order to develop in vitro risk assessment systems for skin sensitization, it is important to predict a threshold from the murine local lymph node assay (LLNA). We first confirmed that the combination of the human Cell Line Activation Test (h-CLAT) and the SH test improved the accuracy and sensitivity of prediction of LLNA data compared with each individual test. Next, we assessed the mutual correlations among maximum amount of change of cell-surface thiols (MAC value) in the SH test, CV75 value (concentration giving 75% cell viability) in a cytotoxicity assay, EC150 and EC200 values (thresholds concentrations of CD86 and CD54 expression, respectively) in h-CLAT and published LLNA thresholds of 64 chemicals. Based on the results, we selected MAC value and the minimum of CV75, EC150 (CD86) and EC200 (CD54) as descriptors for the input layer of an artificial neural network (ANN) system. The ANN-predicted values were well correlated with reported LLNA thresholds. We also found a correlation between the SH test and the peptide-binding assay used to evaluate hapten-protein complex formation. Thus, this model, which we designate as the "iSENS ver. 1", may be useful for risk assessment of skin sensitization potential of chemicals from in vitro test data.

摘要

为了开发皮肤致敏性的体外风险评估系统,从小鼠局部淋巴结试验 (LLNA) 中预测一个阈值是很重要的。我们首先证实,与每个单独的试验相比,人细胞系激活试验 (h-CLAT) 和 SH 试验的组合提高了对 LLNA 数据预测的准确性和敏感性。接下来,我们评估了 SH 试验中细胞表面巯基最大变化量 (MAC 值)、细胞毒性测定中 CV75 值 (导致 75%细胞活力的浓度)、h-CLAT 中 EC150 和 EC200 值 (CD86 和 CD54 表达的阈值浓度) 以及 64 种化学物质公布的 LLNA 阈值之间的相互相关性。基于这些结果,我们选择 MAC 值和 CV75、EC150 (CD86) 和 EC200 (CD54) 的最小值作为人工神经网络 (ANN) 系统输入层的描述符。ANN 预测值与报告的 LLNA 阈值有很好的相关性。我们还发现 SH 试验与用于评估半抗原-蛋白质复合物形成的肽结合测定之间存在相关性。因此,这个模型,我们称之为“iSENS ver. 1”,可能对从体外试验数据评估化学物质的皮肤致敏潜能有用。

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