减少疫苗效力试验中动物数量的方法

Jodie Kulpa-Eddy , Geetha Srinivas
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引用次数: 10

摘要

进行疫苗效力测试是为了在疫苗产品投放市场之前向制造商和监管官员提供有关疫苗产品效力的信息。许可后效力测试方案通常被描述并纳入法规或指导文件。这为制造商提供了一个一致和统一的框架,以遵循市场发布。其中一些协议以广泛接受的国际测试方法为基础;其他的已经存在了几十年,并且是基于当时最好的科学信息。为了确保在活体动物上进行的疫苗测试能提供最佳的动物福利,应考虑并在适当时使用包含减少、替代和改进技术的替代测试方法。罗素和伯奇在《人道实验技术原理》中把减少定义为“减少用于获得一定数量和精度的信息的动物数量”。本文将重点介绍三种减少效价检测动物数量的方法。这些减少方法包括(1)实验设计的改变,(2)基于统计审查的改变,以及(3)由于测试要求的统一而产生的改变。
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Approaches to reducing animal numbers in vaccine potency testing

Vaccine potency testing is conducted to provide manufacturers and regulatory officials information regarding the potency of vaccine products prior to market release. Post-licensing potency test protocols are often described and incorporated into regulation or guidance documents. This provides manufacturers with a consistent and uniform framework to follow for market release. Some of these protocols are based on widely accepted international test methods; others have been in existence for decades and were based on the best scientific information available at that time. In an effort to ensure that vaccine testing conducted on live animals provides optimal animal welfare, alternative test methods incorporating reduction, replacement, and refinement techniques should be considered and used when appropriate. Russell and Burch, in The Principles of Humane Experimental Technique, define reduction as “reduction in the numbers of animals used to obtain information of a given amount and precision.” This paper will focus on three methods of reducing the number of animals used for potency testing. These reduction methods include (1) a change in experimental design, (2) a change based on statistical review, and (3) changes resulting from the harmonization of test requirements.

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