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首页> 外文期刊>Alternatives to laboratory animals: ATLA >Assessment of In Vitro COPD Models for Tobacco Regulatory Science: Workshop Proceedings, Conclusions and Paths Forward for In Vitro Model Use
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Assessment of In Vitro COPD Models for Tobacco Regulatory Science: Workshop Proceedings, Conclusions and Paths Forward for In Vitro Model Use

机译:烟草管制科学的体外COPD模型评估:研讨会论文集,体外模型使用的结论和前进路径

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摘要

The Family Smoking Prevention and Tobacco Control Act of 2009 established the Food and Drug Administration Center for Tobacco Products (FDA-CTP), and gave it regulatory authority over the marketing, manufacture and distribution of tobacco products, including those termed ` modified risk'. On 8-10 December 2014, IIVS organised a workshop conference, entitled Assessment of In Vitro COPD Models for Tobacco Regulatory Science, to bring together stakeholders representing regulatory agencies, academia, industry and animal protection, to address the research priorities articulated by the FDA-CTP. Specific topics were covered to assess the status of current in vitro technologies as they are applied to understanding the adverse pulmonary events resulting from tobacco product exposure, and in particular, the progression of chronic obstructive pulmonary disease (COPD). The four topics covered were: a) Inflammation and Oxidative Stress; b) Ciliary Dysfunction and Ion Transport; c) Goblet Cell Hyperplasia and Mucus Production; and d) Parenchymal/ Bronchial Tissue Destruction and Remodelling. The 2.5 day workshop included 18 expert speakers, plus poster sessions, networking and breakout sessions, which identified key findings and provided recommendations to advance the in vitro technologies and assays used to evaluate tobaccoinduced disease etiologies. The workshop summary was reported at the 2015 Society of Toxicology Annual Meeting, and the recommendations led to an IIVS-organised technical workshop in June 2015, entitled Goblet Cell Hyperplasia, Mucus Production, and Ciliary Beating Assays, to assess these assays and to conduct a proof-of-principle multi-laboratory exercise to determine their suitability for standardisation. Here, we report on the proceedings, recommendations and outcomes of the December 2014 workshop, including paths forward to continue the development of non-animal methods to evaluate tissue responses that model the disease processes that may lead to COPD, a major cause of mortality worldwide.
机译:2009年《防止家庭吸烟和烟草控制法》建立了食品和药物管理局烟草制品管理中心(FDA-CTP),并赋予其对烟草制品的营销,制造和分销的监管权,包括那些被称为“改良风险”的产品。 2014年12月8日至10日,IIVS组织了一个研讨会会议,名为“烟草管制科学的体外COPD模型评估”,召集了代表监管机构,学术界,工业界和动物保护局的利益相关者,以解决FDA-提出的研究重点。 CTP。涵盖了特定主题以评估当前体外技术的状态,因为这些技术被用于了解由烟草制品暴露引起的不良肺事件,尤其是慢性阻塞性肺疾病(COPD)的进展。涵盖的四个主题是:a)炎症和氧化应激; b)睫状功能障碍和离子运输; c)杯状细胞增生和粘液产生; d)实质/支气管组织破坏和重塑。为期2.5天的研讨会包括18位专家演讲者,以及张贴者会议,网络和分组讨论会,这些会议确定了主要发现并提出了建议,以促进用于评估烟草诱发疾病病因的体外技术和测定方法。研讨会总结在2015年毒理学学会年会上进行了报道,这些建议导致在2015年6月由IIVS组织的一次技术研讨会名为“杯状细胞增生,粘液产生和睫状跳动试验”,以评估这些试验并进行原理验证的多实验室练习,以确定其是否适合标准化。在此,我们报告2014年12月研讨会的议事程序,建议和成果,包括继续开发非动物方法以评估组织反应的途径,该方法模拟了可能导致COPD(世界范围内主要死亡原因)的疾病过程。

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