AlphaLISA检测改善疫苗开发过程。

Developments in biologicals Pub Date : 2012-01-01
G Cosentino
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引用次数: 0

摘要

测试疫苗涉及昂贵的动物模型和广泛的体外表征。ELISA和ELISPOT等技术传统上用于测量免疫原性、评估重组疫苗的效力和检测生物污染物的存在。然而,这些久经考验的技术受到影响整个疫苗开发进程的技术限制。限制包括:消耗大量的生物样品(例如;等离子体),高可变性和有限的动态范围。此外,ELISA和ELISPOT涉及大量的阻断和洗涤步骤,这限制了它们的自动化。AlphaLISA技术是一种非常敏感的非洗涤免疫分析平台,减轻了上述所有缺点,使人们能够改善生物制剂的开发过程。将介绍AlphaLISA测定法如何用于评估疫苗效力的例子。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
AlphaLISA assays to improve the vaccine development process.

Testing vaccines involves expensive animal models and extensive in vitro characterization. Techniques such as ELISA and ELISPOT are traditionally used to measure immunogenicity, assess the potency of recombinant vaccines and detect the presence of biological contaminants. However, these time-proven techniques suffer from technical limitations affecting the overall vaccine development process. Limitations include: consumption of large volumes of biological sample (eg. plasma), high variability, and limited dynamic range. Furthermore, ELISA and ELISPOT involve a multitude of blocking and wash steps which limit their automatability. AlphaLISA technology is an exceptionally sensitive non-wash immunoassay platform which alleviates all the aforementioned drawbacks, allowing one to improve biologics development processes. Examples of how AlphaLISA assays can be used to assess the potency of vaccines will be presented.

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