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鱼类疫苗生产与质量控制中的3R方法

Three Rs Approaches in the Production and Quality Control of Fish Vaccines.

作者信息

Midtlyng Paul J, Hendriksen Coenraad, Balks Elisabeth, Bruckner Lukas, Elsken Lawrence, Evensen Oystein, Fyrand Kjetil, Guy Allison, Halder Marlies, Hawkins Penny, Kisen Gunn, Romstad Anne Berit, Salonius Kira, Smith Patrick, Sneddon Lynne U

机构信息

VESO, P.O. Box 300 Sentrum, 0103 Oslo, Norway.

出版信息

Biologicals. 2011 Mar;39(2):117-28. doi: 10.1016/j.biologicals.2011.02.001. Epub 2011 Mar 2.

Abstract

The workshop on Three Rs Approaches in the Production and Quality Control of Fish Vaccines aimed a) to identify animal tests currently stipulated for the production and quality control of fish vaccines and to highlight animal welfare concerns associated with these tests; b) to identify viable options to replace, reduce, and refine animal use for fish vaccine testing; and c) to discuss the way forward and set out how the Three Rs may be implemented without jeopardizing the quality of the vaccines. The workshop participants - experts from academia, regulatory authorities, a scientific animal welfare organization, and the fish vaccine industry - agreed that efforts should be undertaken to replace the vaccination-challenge batch potency testing with tests based on antigen quantification or antibody response tests. Regulatory requirements of questionable scientific value and relevance for the quality of fish vaccines, such as the re-testing of batches produced outside Europe, or the double-dose batch safety test, should be re-considered. As an immediate measure the design of the current animal tests should be evaluated and modified in the light of refinement and reduction, for example, the number of unprotected control fish in vaccination-challenge tests should be reduced to the minimum.

摘要

鱼类疫苗生产与质量控制中的“3R”方法研讨会旨在:a)确定目前鱼类疫苗生产和质量控制规定的动物试验,并强调与这些试验相关的动物福利问题;b)确定可行的选项,以替代、减少和优化鱼类疫苗测试中的动物使用;c)讨论未来方向,并阐述如何在不损害疫苗质量的情况下实施“3R”原则。研讨会参与者——来自学术界、监管机构、科学动物福利组织和鱼类疫苗行业的专家——一致认为,应努力用基于抗原定量或抗体反应测试的方法取代疫苗接种-攻毒批次效力测试。对于鱼类疫苗质量而言,科学价值和相关性存疑的监管要求,如对欧洲以外地区生产的批次进行重新测试,或双剂量批次安全性测试,应重新考虑。作为一项立即采取的措施,应根据优化和减少的原则评估并修改当前动物试验的设计,例如,疫苗接种-攻毒试验中未受保护的对照鱼数量应减至最少。

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