Reliability and relevance of the ES®-RHE model for in vitro skin irritation test application

IF 2.6 3区 医学 Q3 TOXICOLOGY Toxicology in Vitro Pub Date : 2024-09-01 DOI:10.1016/j.tiv.2024.105932
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Abstract

Introduction

In vitro methods have been widely used to assess adverse effects. Reconstructed Human Epidermis (RHE) poses as a fascinating test system employed to assess the dermal irritation hazard potential of chemicals. Although several RHE models are reported in the OECD Test Guideline No. 439, the OECD Document No. 220 encourages the scientific community to develop and validate new RHE test systems due to its relevance for socio-economic advancement.

Methods

Following the criteria documented in the OECD No. 220, a blind study for skin irritation (OECD 439) was conducted employing the Minimum List of Reference Chemicals for Determination of Reproducibility and Predictive Capacity using ES®-RHE. Structural and functional characteristics were assessed alongside the prediction model.

Results

The model has shown reproducibility of optical density and barrier function, similarly to internationally validated methods. Furthermore, it shows the cell layers' development and differentiation ability due to Cytokeratin14, Cytokeratin10, and filaggrin expression. The prediction model resulted in sensitivity, specificity and accuracy rates of 100, 70, and 77 %, respectively.

Conclusions

The ES®-RHE demonstrated reliability and relevance, with similar structural and functional characteristics comparable to internationally validated models, in addition to the accepted predictive capacity according to OECD required minimum criteria, thus confirming the suitability of the national ES®-RHE in the hazard prediction of dermal irritation based on OECD Test Guideline No. 439.

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用于体外皮肤刺激性测试的 ES®-RHE 模型的可靠性和相关性。
介绍:体外方法已被广泛用于评估不良影响。重建人体表皮(RHE)是一种极具吸引力的测试系统,可用于评估化学品的皮肤刺激危害潜力。尽管经合组织第 439 号测试指南中报告了几种 RHE 模型,但由于其与社会经济发展的相关性,经合组织第 220 号文件鼓励科学界开发和验证新的 RHE 测试系统:方法:根据经合组织第 220 号文件中的标准,采用《使用 ES®-RHE 确定重现性和预测能力的参考化学品最低清单》进行了一项皮肤刺激性盲法研究(经合组织第 439 号文件)。对预测模型的结构和功能特性进行了评估:结果:该模型显示了光密度和屏障功能的再现性,与国际验证方法类似。此外,由于细胞角蛋白 14、细胞角蛋白 10 和丝胶蛋白的表达,它还显示了细胞层的发育和分化能力。预测模型的灵敏度、特异性和准确率分别为 100%、70% 和 77%:ES®-RHE具有可靠性和相关性,其结构和功能特征与国际验证的模型相似,此外还具有符合经合组织最低标准要求的公认预测能力,从而证实了国家ES®-RHE适用于根据经合组织第439号试验准则进行皮肤刺激性危害预测。
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来源期刊
Toxicology in Vitro
Toxicology in Vitro 医学-毒理学
CiteScore
6.50
自引率
3.10%
发文量
181
审稿时长
65 days
期刊介绍: Toxicology in Vitro publishes original research papers and reviews on the application and use of in vitro systems for assessing or predicting the toxic effects of chemicals and elucidating their mechanisms of action. These in vitro techniques include utilizing cell or tissue cultures, isolated cells, tissue slices, subcellular fractions, transgenic cell cultures, and cells from transgenic organisms, as well as in silico modelling. The Journal will focus on investigations that involve the development and validation of new in vitro methods, e.g. for prediction of toxic effects based on traditional and in silico modelling; on the use of methods in high-throughput toxicology and pharmacology; elucidation of mechanisms of toxic action; the application of genomics, transcriptomics and proteomics in toxicology, as well as on comparative studies that characterise the relationship between in vitro and in vivo findings. The Journal strongly encourages the submission of manuscripts that focus on the development of in vitro methods, their practical applications and regulatory use (e.g. in the areas of food components cosmetics, pharmaceuticals, pesticides, and industrial chemicals). Toxicology in Vitro discourages papers that record reporting on toxicological effects from materials, such as plant extracts or herbal medicines, that have not been chemically characterized.
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