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比较基因组过敏原快速检测(GARD)测定法与哺乳动物测定法在预测农药活性成分的皮肤致敏潜力方面的预测性质。

Comparison of the predictive nature of the Genomic Allergen Rapid Detection (GARD) assay with mammalian assays in determining the skin sensitisation potential of agrochemical active ingredients.

机构信息

Syngenta, International Research Centre, Jealott's Hill, Bracknell, Berks RG42 6EY, United Kingdom; School of Pharmacy and Biomolecular Sciences, Liverpool John Moores University, Byrom Street, Liverpool L3 3AF, United Kingdom.

Syngenta, International Research Centre, Jealott's Hill, Bracknell, Berks RG42 6EY, United Kingdom; Penman Consulting Limited, Aspect House, Waylands Avenue, Wantage, Oxon OX12 9FF, United Kingdom.

出版信息

Toxicol In Vitro. 2021 Feb;70:105017. doi: 10.1016/j.tiv.2020.105017. Epub 2020 Oct 8.

Abstract

Alternatives to mammalian testing are highly desirable to predict the skin sensitisation potential of agrochemical active ingredients (AI). The GARD assay, a stimulated, dendritic cell-like, cell line measuring genomic signatures, was evaluated using twelve AIs (seven sensitisers and five non-sensitisers) and the results compared with historical results from guinea pig or local lymph node assay (LLNA) studies. Initial GARD results suggested 11/12 AIs were sensitisers and six concurred with mammalian data. Conformal predictions changed one AI to a non-sensitiser. An AI identified as non-sensitising in the GARD assay was considered a potent sensitiser in the LLNA. In total 7/12 GARD results corresponded with mammalian data. AI chemistries might not be comparable to the GARD training set in terms of applicability domains. Whilst the GARD assay can replace mammalian tests for skin sensitisation evaluation for compounds including cosmetic ingredients, further work in agrochemical chemistries is needed for this assay to be a viable replacement to animal testing. The work conducted here is, however, considered exploratory research and the methodology needs further development to be validated for agrochemicals. Mammalian and other alternative assays for regulatory safety assessments of AIs must provide confidence to assign the appropriate classification for human health protection.

摘要

替代哺乳动物测试对于预测农用化学品活性成分 (AI) 的皮肤致敏潜力非常可取。GARD 测定法是一种受刺激的、树突状细胞样的细胞系,用于测量基因组特征,使用 12 种 AI(7 种致敏剂和 5 种非致敏剂)进行了评估,并将结果与豚鼠或局部淋巴结测定法 (LLNA) 研究的历史结果进行了比较。最初的 GARD 结果表明,12 种 AI 中有 11 种是致敏剂,其中 6 种与哺乳动物数据一致。一致性预测将一种 AI 从致敏剂改为非致敏剂。在 GARD 测定法中被鉴定为非致敏剂的 AI 在 LLNA 中被认为是一种强效致敏剂。总共 7/12 的 GARD 结果与哺乳动物数据相符。AI 化学性质在适用性域方面可能与 GARD 训练集不具有可比性。虽然 GARD 测定法可用于评估包括化妆品成分在内的化合物的皮肤致敏性,但是对于该测定法替代动物测试,还需要在农用化学品化学领域进行进一步的工作。然而,这里进行的工作被认为是探索性研究,该方法需要进一步开发,才能在农用化学品方面得到验证。用于 AI 监管安全评估的哺乳动物和其他替代测定法必须为人类健康保护分配适当分类提供信心。

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