a Institute for Translational Vaccinology (Intravacc) , Bilthoven , The Netherlands.
b United States Food and Drug Administration Center for Biologics Evaluation and Research, Silver Spring , MD , USA.
Hum Vaccin Immunother. 2017 Nov 2;13(11):2522-2530. doi: 10.1080/21645515.2017.1349585.
The current test of acellular Bordetella pertussis (aP) vaccines for residual pertussis toxin (PTx) is the Histamine Sensitization test (HIST), based on the empirical finding that PTx sensitizes mice to histamine. Although HIST has ensured the safety of aP vaccines for years, it is criticized for the limited understanding of how it works, its technical difficulty, and for animal welfare reasons. To estimate the number of mice used worldwide for HIST, we surveyed major aP manufacturers and organizations performing, requiring, or recommending the test. The survey revealed marked regional differences in regulatory guidelines, including the number of animals used for a single test. Based on information provided by the parties surveyed, we estimated the worldwide number of mice used for testing to be 65,000 per year: ∼48,000 by manufacturers and ∼17,000 by national control laboratories, although the latter number is more affected by uncertainty, due to confidentiality policies. These animals covered the release of approximately 850 final lots and 250 in-process lots of aP vaccines yearly. Although there are several approaches for HIST refinement and reduction, we discuss why the efforts needed for validation and implementation of these interim alternatives may not be worthwhile, when there are several in vitro alternatives in various stages of development, some already fairly advanced. Upon implementation, one or more of these replacement alternatives can substantially reduce the number of animals currently used for the HIST, although careful evaluation of each alternative's mechanism and its suitable validation will be necessary in the path to implementation.
目前,无细胞百日咳博德特氏菌 (aP) 疫苗残留百日咳毒素 (PTx) 的检测方法是组胺致敏试验 (HIST),这一方法基于 PTx 使小鼠致敏于组胺的经验性发现。尽管 HIST 多年来确保了 aP 疫苗的安全性,但它因对其工作原理的理解有限、技术难度以及出于动物福利的原因而受到批评。为了估计全球用于 HIST 的小鼠数量,我们调查了主要的 aP 制造商和进行、要求或推荐该检测的组织。调查显示,监管指南存在明显的区域差异,包括单次检测使用的动物数量。根据被调查方提供的信息,我们估计全球用于检测的小鼠数量为每年 65,000 只:制造商使用约 48,000 只,国家控制实验室使用约 17,000 只,尽管由于保密政策,后者的数量受不确定性影响更大。这些动物涵盖了每年约 850 个最终批次和 250 个 aP 疫苗中间批次的放行。尽管 HIST 有几种改进和减少的方法,但我们讨论了为什么在有几种处于不同开发阶段的替代物的情况下,验证和实施这些临时替代物的努力可能不值得,其中一些替代物已经相当先进。一旦实施,这些替代物中的一种或多种可以大大减少目前用于 HIST 的动物数量,尽管在实施过程中需要对每种替代物的机制及其适当的验证进行仔细评估。