Mizumachi Hideyuki, Suzuki Sho, Sakuma Megumi, Natsui Midori, Imai Noriyasu, Miyazawa Masaaki
Safety Science Research, Kao Corporation, Haga-gun, Japan.
Safety and Analytical Research Laboratories, KOSÉ Corporation, Tokyo, Japan.
J Appl Toxicol. 2024 Mar;44(3):415-427. doi: 10.1002/jat.4551. Epub 2023 Oct 17.
The hazards and potency of skin sensitizers are traditionally determined using animal tests such as the local lymph node assay (LLNA); however, significant progress has been made in the development of non-animal test methods addressing the first three mechanistic key events of adverse outcome pathway in skin sensitization. We developed the epidermal sensitization assay (EpiSensA), which is a reconstructed human epidermis-based assay, by measuring four genes related to critical keratinocyte responses during skin sensitization. Four in vitro skin sensitization test methods (EpiSensA, direct peptide reactivity assay [DPRA], KeratinoSens™, and human cell line activation test [h-CLAT]) were systematically evaluated using 136 chemicals including lipophilic chemicals and pre/pro-haptens, which may be related to assay-specific limitations. The constructed database included existing and newly generated data. The EpiSensA showed a broader applicability domain and predicted the hazards with 82.4% and 78.8% accuracy than LLNA and human data. The EpiSensA could detect 76 out of 88 sensitizers at lower concentrations than the LLNA, indicating that the EpiSensA has higher sensitivity for the detection of minor sensitizing constituents. These results confirmed the potential use of the EpiSensA in evaluating a mixture of unknown compositions that can be evaluated by animal tests. To combine different information sources, the reconstructed human epidermis-based testing strategy (RTS) was developed based on weighted multiple information from the EpiSensA and TImes MEtabolism Simulator platform for predicting Skin Sensitization (TIMES-SS; RTSv1) or Organization for Economic Cooperation and Development (OECD) QSAR Toolbox automated workflow (RTSv2). The predictivities of the hazards and Globally Harmonized System (GHS) subcategories were equal to or better than the defined approaches (2 out of 3, integrated testing strategy [ITS]v1, and ITSv2) adopted as OECD Guideline 497.
传统上,皮肤致敏剂的危害和效力是通过动物试验来确定的,如局部淋巴结试验(LLNA);然而,在开发针对皮肤致敏不良结局途径前三个机制关键事件的非动物试验方法方面已经取得了重大进展。我们开发了表皮致敏试验(EpiSensA),这是一种基于重建人表皮的试验,通过测量与皮肤致敏过程中关键角质形成细胞反应相关的四个基因来进行。使用136种化学物质(包括亲脂性化学物质和前体/半抗原,这些可能与特定试验的局限性有关)对四种体外皮肤致敏试验方法(EpiSensA、直接肽反应性试验[DPRA]、KeratinoSens™和人细胞系激活试验[h-CLAT])进行了系统评估。构建的数据库包括现有数据和新生成的数据。EpiSensA显示出更广泛的适用范围,预测危害的准确率比LLNA和人类数据分别高82.4%和78.8%。EpiSensA能够在比LLNA更低的浓度下检测出88种致敏剂中的76种,这表明EpiSensA在检测微量致敏成分方面具有更高的灵敏度。这些结果证实了EpiSensA在评估可通过动物试验进行评估的未知成分混合物方面的潜在用途。为了整合不同的信息来源,基于来自EpiSensA的加权多重信息以及用于预测皮肤致敏的时间代谢模拟器平台(TIMES-SS;RTSv1)或经济合作与发展组织(OECD)QSAR工具箱自动化工作流程(RTSv2),开发了基于重建人表皮的测试策略(RTS)。危害预测和全球协调系统(GHS)子类别的预测能力等于或优于作为经合组织准则497采用的既定方法(3种方法中的2种,综合测试策略[ITS]v1和ITSv2)。