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基于遗传修饰细胞的生物制品效价检测方法的建立与应用。

Development and application of potency assays based on genetically modified cells for biological products.

机构信息

Key Laboratory of the Ministry of Health for Research on Quality and Standardization of Biotech Products, National Institutes for Food and Drug Control, No. 2, Tiantan Xili, Dongcheng District, Beijing 100050, China.

Key Laboratory of the Ministry of Health for Research on Quality and Standardization of Biotech Products, National Institutes for Food and Drug Control, No. 2, Tiantan Xili, Dongcheng District, Beijing 100050, China.

出版信息

J Pharm Biomed Anal. 2023 Jun 15;230:115397. doi: 10.1016/j.jpba.2023.115397. Epub 2023 Apr 14.

Abstract

Potency assays are key to the development, registration, and quality control of biological products. Although previously preferred for clinical relevance, in vivo bioassays have greatly diminished with the advent of dependent cell lines as well as due to ethical concerns. However, for some products, the development of in vitro cell-based assay is challenging, or existing method has limitations such as tedious procedure or low sensitivity. The generation of genetically modified (GM) cell line with improved response to the analyte provides a scientific and promising solution. Potency assays based on GM cell lines are currently used for the quality control of biological products including cytokines, hormones, therapeutic antibodies, vaccines and gene therapy products. In this review, we have discussed the general principles of designing and developing GM cells-based potency assays, including identification of cellular signaling pathways and detectable biological effects, generation of responsive cell lines and constitution of test systems, based on the current research progress. In addition, the applications of some novel technologies and the common concerns regarding GM cells have also been discussed. The research presented in this review provides insights for the development and application of novel GM cells-based potency assays for biological products.

摘要

效价测定是生物制品研发、注册和质量控制的关键。尽管体内生物测定法以前因其与临床的相关性而被优先选用,但随着依赖细胞系的出现以及出于伦理方面的考虑,其应用已大大减少。然而,对于某些产品,开发基于体外细胞的测定法具有挑战性,或者现有的方法存在繁琐的程序或低灵敏度等局限性。具有改善对分析物反应的遗传修饰(GM)细胞系的产生为解决这一问题提供了科学和有前途的方法。基于 GM 细胞系的效价测定法目前用于生物制品的质量控制,包括细胞因子、激素、治疗性抗体、疫苗和基因治疗产品。在这篇综述中,我们根据当前的研究进展,讨论了设计和开发基于 GM 细胞系的效价测定法的一般原则,包括鉴定细胞信号通路和可检测的生物学效应、产生有反应性的细胞系和构建测试系统。此外,还讨论了一些新技术的应用以及 GM 细胞的常见关注点。本综述中介绍的研究为生物制品新型 GM 细胞系效价测定法的开发和应用提供了思路。

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