| Literature DB >> 34568831 |
Mohamed Abou-El-Enein1,2, Magdi Elsallab2, Gerhard Bauer3, Barbara Savoldo4, Steven A Feldman5, Andrew D Fesnak6,7, Helen E Heslop8, Peter Marks9, Brian G Till10.
Abstract
As of April 2021, there are five commercially available chimeric antigen receptor (CAR) T cell therapies for hematological malignancies. With the current transition of CAR T cell manufacturing from academia to industry, there is a shift toward Good Manufacturing Practice (GMP)-compliant closed and automated systems to ensure reproducibility and to meet the increased demand for cancer patients. In this review we describe current CAR T cells clinical manufacturing models and discuss emerging technological advances that embrace scaling and production optimization. We summarize measures being used to shorten CAR T-cell manufacturing times and highlight regulatory challenges to scaling production for clinical use. STATEMENT OF SIGNIFICANCE ∣: As the demand for CAR T cell cancer therapy increases, several closed and automated production platforms are being deployed, and others are in development.This review provides a critical appraisal of these technologies that can be leveraged to scale and optimize the production of next generation CAR T cells.Entities:
Keywords: Automation; CAR T cells; Clinical Production; GMP; Genetic Modification; Hematological Malignancies; Manufacturing; Scaling; Solid Tumors
Mesh:
Year: 2021 PMID: 34568831 PMCID: PMC8462122 DOI: 10.1158/2643-3230.BCD-21-0084
Source DB: PubMed Journal: Blood Cancer Discov ISSN: 2643-3230