| Literature DB >> 30543841 |
Xiaofeng Dai1, Yi Mei2, Dongyan Cai3, Weidong Han4.
Abstract
CAR-T therapy, grafting the specificity of a monoclonal antibody onto a T cell to target certain cancer cells, has been recognized as a promising therapeutic approach for cancer control as evidenced by the two CAR-T products proved by FDA in 2017. However, the unique heterogeneity of CAR-T therapy has restricted its production in a limited number of institutions and made it a boutique oncotherapy. By reviewing outstanding issues surrounding the commercial scale production of CAR-T therapy, we conclude that achieving mass production of CAR-T therapy without sacrificing its personalized nature is a worldwild challenge for making CAR-T a key element in the next generation of precision medicine, which can be achieved by standardizing 7 prominent factors that collectively determine the scale of CAR-T manufacturing.Entities:
Keywords: Ancillary reagents; Chimeric antigen receptor; Government regulation; Manufacturing process; Post-treatment immune monitoring; Quality control; Source materials; Standardization; Viral vectors
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Year: 2018 PMID: 30543841 DOI: 10.1016/j.biotechadv.2018.12.002
Source DB: PubMed Journal: Biotechnol Adv ISSN: 0734-9750 Impact factor: 14.227