Ayehunie Seyoum, Snell Maureen, Child Matthew, Klausner Mitchell
MatTek Corporation, Ashland, MA 01721, United States.
Toxicology. 2009 Oct 1;264(1-2):1-9. doi: 10.1016/j.tox.2009.07.021. Epub 2009 Aug 7.
A predictive allergenicity test system for assessing the contact allergenicity of chemicals is needed by the cosmetic and pharmaceutical industry to monitor product safety in the marketplace. Development of such non-animal alternative assay systems for skin sensitization and hazard identification has been pursued by policy makers and regulatory agencies. We investigated whether phenotypic and functional changes to a subset of dendritic cells (DC), plasmacytoid DC (pDC), could be used to identify contact allergens. To achieve this goal, normal human DC were generated from CD34+ progenitor cells and cryopreserved. Frozen DC were thawed and the pDC fraction (CD123+/CD11c-) was harvested using FACS sorting. The pDC were cultured, expanded, and exposed to chemical allergens (N=26) or non-allergens (N=22). Concentrations of each chemical that resulted in >50% viability was determined using FACS analysis of propidium iodide stained cells using pDC from 2 to 5 donors. Expression of the surface marker, CD86, which has been implicated in dendritic cell maturation, was used as a marker of allergenicity. CD86 expression increased (> or =1.5-fold) for 25 of 26 allergens (sensitivity=96%) but did not increase for 19 of 22 non-allergens (specificity=86%). In a direct comparison to historical data for the regulatory approved, mouse local lymph node assay (LLNA) for 23 allergens and 22 non-allergens, the pDC method had sensitivity and specificity of 96% and 86%, respectively, while the sensitivity and specificity of the LLNA assay was 83% and 82%, respectively. In conclusion, CD86 expression in pDC appears to be a sensitive and specific indicator to identify contact allergenicity. Such an assay method utilizing normal human cells will be useful for high throughput screening of chemicals for allergenicity.
化妆品和制药行业需要一种用于评估化学品接触致敏性的预测性致敏性测试系统,以监测市场上产品的安全性。政策制定者和监管机构一直在寻求开发这种用于皮肤致敏和危害识别的非动物替代检测系统。我们研究了树突状细胞(DC)亚群,即浆细胞样DC(pDC)的表型和功能变化是否可用于识别接触性过敏原。为实现这一目标,从CD34+祖细胞生成正常人DC并进行冷冻保存。解冻冷冻的DC,使用荧光激活细胞分选(FACS)分选收获pDC部分(CD123+/CD11c-)。培养、扩增pDC,并使其暴露于化学过敏原(N = 26)或非过敏原(N = 22)。使用来自2至5名供体的pDC,通过碘化丙啶染色细胞的FACS分析确定每种导致>50%活力的化学物质的浓度。表面标志物CD86的表达与树突状细胞成熟有关,用作致敏性的标志物。26种过敏原中有25种(敏感性 = 96%)的CD86表达增加(≥1.5倍),但22种非过敏原中有19种的CD86表达未增加(特异性 = 86%)。与监管批准的用于23种过敏原和22种非过敏原的小鼠局部淋巴结试验(LLNA)的历史数据直接比较,pDC方法的敏感性和特异性分别为96%和86%,而LLNA试验的敏感性和特异性分别为83%和82%。总之,pDC中CD86的表达似乎是识别接触致敏性的敏感且特异的指标。这种利用正常人细胞的检测方法将有助于高通量筛选化学品的致敏性。