Overview of currently approved veterinary vaccine potency testing methods and methods in development that do not require animal use

Hans Draayer
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引用次数: 17

Abstract

Veterinary vaccines must be safe, pure, potent, and effective. Potency tests help ensure that each consistently manufactured batch of vaccine provides a level of protection as determined in the original efficacy study throughout the products shelf life. Currently approved assays range from host animal vaccination and challenge to the quantification of specific protective antigens using in vitro technology. The development, maintenance, and update of in vitro potency assays continue to be a priority for both the animal health industry and the corresponding regulatory agencies. New assay development emphasis is being placed on assays that currently involve laboratory animal vaccination/challenge such as vaccines containing the Leptospira and Clostridium spp. antigens. This paper provides an overview of various in vitro potency assays available, the factors that can impact the accuracy of these methods, and specific considerations to be taken into account during assay development.

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概述目前批准的兽医疫苗效力测试方法和正在开发的不需要动物使用的方法
兽医疫苗必须是安全、纯净、强效和有效的。效力测试有助于确保每一批一贯生产的疫苗在整个产品保质期内都能提供原始功效研究中确定的保护水平。目前批准的检测方法包括从宿主动物疫苗接种和挑战到使用体外技术对特定保护性抗原进行定量。体外效力测定法的开发、维护和更新仍然是动物保健行业和相应监管机构的优先事项。新的检测开发的重点是目前涉及实验室动物疫苗接种/挑战的检测,例如含有钩端螺旋体和梭状芽孢杆菌抗原的疫苗。本文概述了各种可用的体外效力测定法,可能影响这些方法准确性的因素,以及在测定开发过程中要考虑的具体因素。
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