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

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.

Keywords: Biological products; Genetically modified cell line; Potency assay; Reporter gene assay.

Publication types

  • Review

MeSH terms

  • Biological Assay / methods
  • Biological Factors
  • Biological Products* / pharmacology
  • Cytokines
  • Quality Control

Substances

  • Biological Products
  • Biological Factors
  • Cytokines