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半抗原-蛋白质结合:从理论到体外皮肤致敏预测的实际应用

Hapten-protein binding: from theory to practical application in the in vitro prediction of skin sensitization.

作者信息

Divkovic Maja, Pease Camilla K, Gerberick G Frank, Basketter David A

机构信息

Unilever Colworth, Sharnbrook, Bedfordshire, UK.

出版信息

Contact Dermatitis. 2005 Oct;53(4):189-200. doi: 10.1111/j.0105-1873.2005.00683.x.

Abstract

In view of the forthcoming European Union ban on in vivo testing of cosmetic and toiletry ingredients, following the publication of the 7th amendment to the Cosmetics Directive, the search for practical, alternative, non-animal approaches is gathering pace. For the end-point of skin sensitization, the ultimate goal, i.e. the development and validation of alternative in vitro/in silico assays by 2013, may be achieved through a better understanding of the skin sensitization process on the cellular and molecular levels. One of the key molecular events in skin sensitization is protein haptenation, i.e. the chemical modification of self-skin protein(s) thus forming macromolecular immunogens. This concept is widely accepted and in theory can be used to explain the sensitizing capacity of many known skin sensitizers. Thus, the principle of protein or peptide haptenation could be used in in vitro assays to predict the sensitization potential of a new chemical entity. In this review, we consider some of the theoretical aspects of protein haptenation, how mechanisms of protein haptenation can be investigated experimentally and how we can use such knowledge in the development of novel, alternative approaches for predicting skin sensitization potential in the future.

摘要

鉴于随着《化妆品指令》第7次修订案的公布,欧盟即将禁止对化妆品和洗漱用品成分进行体内试验,寻找实用、替代、非动物的方法的步伐正在加快。对于皮肤致敏这一终点而言,最终目标,即在2013年前开发并验证替代的体外/计算机模拟试验,或许可以通过在细胞和分子水平上更好地理解皮肤致敏过程来实现。皮肤致敏过程中的关键分子事件之一是蛋白质半抗原化,即自身皮肤蛋白质的化学修饰,从而形成大分子免疫原。这一概念已被广泛接受,理论上可用于解释许多已知皮肤致敏剂的致敏能力。因此,蛋白质或肽半抗原化的原理可用于体外试验,以预测新化学实体的致敏潜力。在本综述中,我们探讨了蛋白质半抗原化的一些理论方面,如何通过实验研究蛋白质半抗原化的机制,以及我们如何在未来开发预测皮肤致敏潜力的新型替代方法中运用这些知识。

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