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体外检测接触过敏原:使用人外周血单核细胞来源的树突状细胞优化方案的开发。

In vitro detection of contact allergens: development of an optimized protocol using human peripheral blood monocyte-derived dendritic cells.

机构信息

Research and Development, Beiersdorf AG, Hamburg, Germany.

出版信息

Toxicol In Vitro. 2011 Feb;25(1):315-23. doi: 10.1016/j.tiv.2010.09.016. Epub 2010 Oct 29.

Abstract

Allergic contact dermatitis is a delayed T-cell mediated allergic response associated with relevant social and economic impacts. Animal experiments (e.g. the local lymph node assay) are still supplying most of the data used to assess the sensitization potential of new chemicals. However, the 7th amendment to the EU Cosmetic Directive will introduce a testing ban for cosmetic ingredients after 2013. In vitro alternative methods are thus being actively developed. Although promising results have been obtained with cell lines, their reduced functionality and inherent genomic instability led us to reinvestigate the use of peripheral blood monocyte-derived dendritic cells (PBMDCs) for the establishment of a reliable in vitro sensitization test. To solve the issues associated with the use of primary cells, the culture and exposure conditions (cytokine concentrations, incubation time, readout, pooled vs. single donors and cytotoxicity) were re-assessed and optimized. Here we propose a stable and reproducible protocol based on PBMDCs. This should allow a wider acceptance of PBMDCs as a reliable test system for the detection of human skin sensitizers and the inclusion of this protocol in an integrated testing strategy.

摘要

变应性接触性皮炎是一种迟发型 T 细胞介导的过敏反应,与相关的社会和经济影响有关。动物实验(如局部淋巴结试验)仍在提供大多数用于评估新化学物质致敏潜力的数据。然而,欧盟化妆品指令的第 7 修正案将在 2013 年后禁止对化妆品成分进行测试。因此,正在积极开发体外替代方法。尽管细胞系已经取得了有希望的结果,但由于其功能降低和固有的基因组不稳定性,我们重新研究了使用外周血单核细胞衍生的树突状细胞(PBMDC)建立可靠的体外致敏试验。为了解决使用原代细胞相关的问题,我们重新评估和优化了培养和暴露条件(细胞因子浓度、孵育时间、读出、混合供体与单个供体和细胞毒性)。在这里,我们提出了一个基于 PBMDC 的稳定且可重复的方案。这应该允许更广泛地接受 PBMDC 作为检测人类皮肤致敏剂的可靠测试系统,并将该方案纳入综合测试策略中。

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