Patlewicz Grace, Casati Silvia, Basketter David A, Asturiol David, Roberts David W, Lepoittevin Jean-Pierre, Worth Andrew P, Aschberger Karin
US Environmental Protection Agency, National Center for Computational Toxicology, Research Triangle Park, NC, USA.
European Commission, Joint Research Centre, Directorate F - Health, Consumers and Reference Materials, Chemical Safety and Alternative Methods Unit, Ispra, VA, Italy.
Regul Toxicol Pharmacol. 2016 Dec;82:147-155. doi: 10.1016/j.yrtph.2016.08.007. Epub 2016 Aug 26.
Predictive testing to characterize substances for their skin sensitization potential has historically been based on animal tests such as the Local Lymph Node Assay (LLNA). In recent years, regulations in the cosmetics and chemicals sectors have provided strong impetus to develop non-animal alternatives. Three test methods have undergone OECD validation: the direct peptide reactivity assay (DPRA), the KeratinoSens™ and the human Cell Line Activation Test (h-CLAT). Whilst these methods perform relatively well in predicting LLNA results, a concern raised is their ability to predict chemicals that need activation to be sensitizing (pre- or pro-haptens). This current study reviewed an EURL ECVAM dataset of 127 substances for which information was available in the LLNA and three non-animal test methods. Twenty eight of the sensitizers needed to be activated, with the majority being pre-haptens. These were correctly identified by 1 or more of the test methods. Six substances were categorized exclusively as pro-haptens, but were correctly identified by at least one of the cell-based assays. The analysis here showed that skin metabolism was not likely to be a major consideration for assessing sensitization potential and that sensitizers requiring activation could be identified correctly using one or more of the current non-animal methods.
历史上,用于表征物质皮肤致敏潜力的预测性测试一直基于动物试验,如局部淋巴结试验(LLNA)。近年来,化妆品和化学品行业的法规有力推动了非动物替代方法的开发。有三种测试方法已通过经合组织(OECD)验证:直接肽反应性测定法(DPRA)、KeratinoSens™ 和人细胞系激活试验(h-CLAT)。虽然这些方法在预测LLNA结果方面表现相对良好,但人们担心它们预测需要激活才能致敏的化学物质(前体或前半抗原)的能力。本研究回顾了欧洲替代方法验证中心(EURL ECVAM)的一个包含127种物质的数据集,这些物质在LLNA和三种非动物测试方法方面都有可用信息。其中28种致敏剂需要激活,大多数是前体。这些物质被1种或更多测试方法正确识别。有6种物质被专门归类为前半抗原,但至少被一种基于细胞的试验正确识别。此处的分析表明,皮肤代谢不太可能是评估致敏潜力的主要考虑因素,并且使用一种或多种当前的非动物方法可以正确识别需要激活的致敏剂。