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从局部淋巴结试验剂量反应推导EC3值的统计方法比较。

A comparison of statistical approaches to the derivation of EC3 values from local lymph node assay dose responses.

作者信息

Basketter D A, Lea L J, Dickens A, Briggs D, Pate I, Dearman R J, Kimber I

机构信息

Safety and Environmental Assurance Centre, Unilever Research, Sharnbrook, UK.

出版信息

J Appl Toxicol. 1999 Jul-Aug;19(4):261-6. doi: 10.1002/(sici)1099-1263(199907/08)19:4<261::aid-jat572>3.0.co;2-5.

DOI:10.1002/(sici)1099-1263(199907/08)19:4<261::aid-jat572>3.0.co;2-5
PMID:10439340
Abstract

Effective risk assessment and management of allergic contact dermatitis require three key factors: adequate hazard identification, measurement of the relative potency of identified hazards and an understanding of the nature, extent and duration of exposure. Suitable methods for hazard identification, such as the murine local lymph node assay (LLNA) and the guinea-pig maximization test, are well established and conditions of human exposure normally can be well anticipated. Thus, the need is for a robust and quantitative method for the estimation of relative skin sensitizing potency. One possible approach is via the analysis of LLNA dose-response data. In the LLNA, contact allergens are defined currently as those chemicals that cause a threefold or greater increase in lymph node cell proliferative activity compared with concurrent vehicle-treated controls. It is possible to estimate the concentration of a sensitizer required to generate a threefold stimulation of proliferation in draining lymph nodes; such a concentration is known as the EC3 value. Using a variety of statistical approaches to derive EC3 values from LLNA dose-response data for 10 chemicals, it has been demonstrated that simple linear interpolation between the values either side of the threefold stimulation index provides a robust assessment of the EC3 value without the need for recourse to more sophisticated statistical techniques. Provided that the appropriate concentrations of test chemical have been selected, EC3 values obtained in this way are reproducible both within and between laboratories and form the basis for examination of the utility of this approach for the estimation of relative skin sensitizing potency.

摘要

过敏性接触性皮炎的有效风险评估和管理需要三个关键因素

充分的危害识别、对已识别危害相对强度的测量以及对接触的性质、程度和持续时间的了解。用于危害识别的合适方法,如小鼠局部淋巴结试验(LLNA)和豚鼠最大化试验,已经确立,并且通常可以很好地预测人体接触条件。因此,需要一种可靠的定量方法来估计相对皮肤致敏强度。一种可能的方法是通过分析LLNA剂量反应数据。在LLNA中,接触性过敏原目前被定义为与同时用赋形剂处理的对照相比,能使淋巴结细胞增殖活性增加三倍或更多的那些化学物质。可以估计在引流淋巴结中产生三倍增殖刺激所需的致敏剂浓度;这样的浓度被称为EC3值。使用多种统计方法从10种化学物质的LLNA剂量反应数据中得出EC3值,结果表明,在三倍刺激指数两侧的值之间进行简单的线性插值,无需借助更复杂的统计技术,就能对EC3值进行可靠评估。只要选择了合适浓度的受试化学物质,以这种方式获得的EC3值在实验室内和实验室间都是可重复的,并且构成了检验这种方法用于估计相对皮肤致敏强度效用的基础。

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