Improved harmonization of critical characterization assays across cell therapies

被引:10
|
作者
Karanu, Francis [1 ]
Ott, Lindsey [1 ]
Webster, Debra Aub [2 ]
Stehno-Bittel, Lisa [1 ,3 ]
机构
[1] Likarda LLC, 10330 Hickman Mills Dr, Kansas City, MO 64137 USA
[2] Cardinal Hlth Regulatory Sci, 7400 West 100th St, Overland Pk, KS 66210 USA
[3] Univ Kansas, Med Ctr, Dept Rehabil Sci, MS 2002,3901 Rainbow Blvd, Kansas City, MO USA
关键词
cell therapy; embryonic stem cells; hematopoetic stem cells; induced pluripotent stem cells; industry; manufacturing; mesenchymal stromal cells; regulation; MESENCHYMAL STROMAL CELLS; BONE-MARROW; STEM-CELLS; MICROBIAL-CONTAMINATION; BACTERIAL-CONTAMINATION; ISLET TRANSPLANTATION; INTERNATIONAL-SOCIETY; SURFACE-MARKERS; RISK-FACTORS; IDENTIFICATION;
D O I
10.2217/rme-2020-0003
中图分类号
Q813 [细胞工程];
学科分类号
摘要
The field of cell therapy has blossomed, providing exciting new options for treating a variety of diseases. While few cell therapy products have US FDA approval, there are thousands of cell treatments at various stages of development, pointing to a potential revolutionary shift in patient care. The expanding number and nature of cellular therapies necessitate greater standardization. Several international organizations are collaborating to pursue some level of global standardization, especially concerning cell banking. However, less harmonization surrounds assays used for critical quality characterization including: identity, purity, safety and potency. Frequently, there is divergence regarding the terms describing the characterization assays across regulatory authorities and guidances. This review summarizes the critical quality assays currently used for different categories of cell therapies. Areas of harmonization and an absence of standardization are highlighted. We propose potential solutions to facilitate harmonization of critical quality characterization assays and the language used to describe them.
引用
收藏
页码:1661 / 1678
页数:18
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