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局部淋巴结法变异性:全面评估非动物皮肤致敏试验方法和策略的关键要素。

LLNA variability: An essential ingredient for a comprehensive assessment of non-animal skin sensitization test methods and strategies.

作者信息

Hoffmann Sebastian

机构信息

seh consulting + services, Paderborn, Germany.

出版信息

ALTEX. 2015;32(4):379-83. doi: 10.14573/altex.1505051. Epub 2015 Jul 13.

Abstract

The development of non-animal skin sensitization test methods and strategies is quickly progressing. Either individually or in combination, the predictive capacity is usually described in comparison to local lymph node assay (LLNA) results. In this process the important lesson from other endpoints, such as skin or eye irritation, to account for variability reference test results - here the LLNA - has not yet been fully acknowledged. In order to provide assessors as well as method and strategy developers with appropriate estimates, we investigated the variability of EC3 values from repeated substance testing using the publicly available NICEATM (NTP Interagency Center for the Evaluation of Alternative Toxicological Methods) LLNA database. Repeat experiments for more than 60 substances were analyzed - once taking the vehicle into account and once combining data over all vehicles. In general, variability was higher when different vehicles were used. In terms of skin sensitization potential, i.e., discriminating sensitizer from non-sensitizers, the false positive rate ranged from 14-20%, while the false negative rate was 4-5%. In terms of skin sensitization potency, the rate to assign a substance to the next higher or next lower potency class was approx.10-15%. In addition, general estimates for EC3 variability are provided that can be used for modelling purposes. With our analysis we stress the importance of considering the LLNA variability in the assessment of skin sensitization test methods and strategies and provide estimates thereof.

摘要

非动物皮肤致敏试验方法和策略的发展正在迅速推进。无论是单独还是组合使用,其预测能力通常是与局部淋巴结试验(LLNA)结果相比较来描述的。在此过程中,从其他终点(如皮肤或眼睛刺激性)中吸取的关于考虑参考试验结果变异性(此处为LLNA)的重要教训尚未得到充分认识。为了给评估人员以及方法和策略开发者提供适当的估计,我们使用公开可用的NICEATM(美国国家毒理学计划跨机构替代毒理学方法评估中心)LLNA数据库,研究了重复物质测试中EC3值的变异性。分析了60多种物质的重复实验——一次考虑赋形剂,一次合并所有赋形剂的数据。一般来说,使用不同赋形剂时变异性更高。就皮肤致敏潜力而言,即区分致敏剂和非致敏剂,假阳性率在14%至20%之间,而假阴性率为4%至5%。就皮肤致敏强度而言,将一种物质归为下一个更高或更低强度类别的比率约为10%至15%。此外,还提供了可用于建模目的的EC3变异性的一般估计。通过我们的分析,我们强调了在评估皮肤致敏试验方法和策略时考虑LLNA变异性的重要性,并提供了相关估计。

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