dos Santos G Galvão, Reinders J, Ouwehand K, Rustemeyer T, Scheper R J, Gibbs S
Department of Dermatology, VU University Medical Centre, Amsterdam, The Netherlands.
Toxicol Appl Pharmacol. 2009 May 1;236(3):372-82. doi: 10.1016/j.taap.2009.02.004. Epub 2009 Feb 14.
Allergic contact dermatitis is the result of an adaptive immune response of the skin to direct exposure to an allergen. Since many chemicals are also allergens, European regulations require strict screening of all ingredients in consumer products. Until recently, identifying a potential allergen has completely relied on animal testing (e.g.: Local Lymph Node Assay). In addition to the ethical problems, both the 7th Amendment to the Cosmetics Directive and REACH have stimulated the development of alternative tests for the assessment of potential sensitizers. This review is aimed at summarising the progress on cell based assays, in particular dendritic cell based assays, being developed as animal alternatives. Primary cells (CD34(+) derived dendritic cells, monocyte derived dendritic cells) as well as dendritic cell-like cell lines (THP-1, U-937, MUTZ-3, KG-1, HL-60, and K562) are extensively described along with biomarkers such as cell surface markers, cytokines, chemokines and kinases. From this review, it can be concluded that no single cell based assay nor single marker is yet able to distinguish all sensitizers from non-sensitizers in a test panel of chemicals, nor is it possible to rank the sensitizing potential of the test chemicals. This suggests that sensitivity and specificity may be increased by a tiered assay approach. Only a limited number of genomic and proteomic studies have been completed until now. Such studies have the potential to identify novel biomarkers for inclusion in future assay development. Although progress is promising, this review suggests that it may be difficult to meet the up and coming European regulatory deadlines.
过敏性接触性皮炎是皮肤对直接接触过敏原产生适应性免疫反应的结果。由于许多化学物质也是过敏原,欧洲法规要求对消费品中的所有成分进行严格筛选。直到最近,识别潜在过敏原完全依赖于动物试验(例如:局部淋巴结试验)。除了伦理问题外,《化妆品指令》第7次修订案和《化学品注册、评估、授权和限制法规》(REACH)都推动了用于评估潜在致敏剂的替代试验的发展。本综述旨在总结作为动物替代试验正在开发的基于细胞的试验,特别是基于树突状细胞的试验的进展。原代细胞(CD34(+)衍生的树突状细胞、单核细胞衍生的树突状细胞)以及树突状细胞样细胞系(THP-1、U-937、MUTZ-3、KG-1、HL-60和K562)以及细胞表面标志物、细胞因子、趋化因子和激酶等生物标志物都有广泛描述。从本综述可以得出结论,在一组化学物质的试验中,没有一种基于细胞的试验或单一标志物能够将所有致敏剂与非致敏剂区分开来,也不可能对受试化学物质的致敏潜力进行排名。这表明通过分层试验方法可能会提高敏感性和特异性。到目前为止,仅完成了数量有限的基因组和蛋白质组学研究。此类研究有潜力识别新的生物标志物,以纳入未来的试验开发中。尽管进展令人鼓舞,但本综述表明,可能难以满足即将到来的欧洲监管期限。