Associação Brasileira de Hematologia, Hemoterapia e Terapia Celular Consensus on genetically modified cells. VII. Present and future of technologies for production of CAR cell therapies
Chimeric Antigen Receptor T (CAR-T) cells are certainly an important therapy for patients with relapsed and/or refractory hematologic malignancies. Currently, there are five CAR-T cell products approved by the FDA but several research groups and/or biopharmaceutical companies are encouraged to devel...
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oai:doaj.org-article:558a6b96477e4bcba2af415589f2cdde2021-11-18T04:51:04ZAssociação Brasileira de Hematologia, Hemoterapia e Terapia Celular Consensus on genetically modified cells. VII. Present and future of technologies for production of CAR cell therapies2531-137910.1016/j.htct.2021.09.007https://doaj.org/article/558a6b96477e4bcba2af415589f2cdde2021-11-01T00:00:00Zhttp://www.sciencedirect.com/science/article/pii/S2531137921001413https://doaj.org/toc/2531-1379Chimeric Antigen Receptor T (CAR-T) cells are certainly an important therapy for patients with relapsed and/or refractory hematologic malignancies. Currently, there are five CAR-T cell products approved by the FDA but several research groups and/or biopharmaceutical companies are encouraged to develop new products based on CAR cells using T or other cell types. Production of CAR cells requires intensive work from the basic, pre-clinical to translational levels, aiming to overcome technical difficulties and failure in the production. At least five key common steps are needed for the manipulation of T-lymphocytes (or other cells), such as: cell type selection, activation, gene delivery, cell expansion and final product formulation. However, reproducible manufacturing of high-quality clinical-grade CAR cell products is still required to apply this technology to a greater number of patients. This chapter will discuss the present and future development of new CAR designs that are safer and more effective to improve this therapy, achieving more selective killing of malignant cells and less toxicity to be applied in the clinical setting.Rodrigo Nalio RamosVirginia Picanço-CastroTheo Gremen M. OliveiraAlfredo Mendrone, JuniorGil Cunha De SantisMartin Hernan BonaminoVanderson RochaElsevierarticleNew technologiesCAR cell therapiesManufacturingGene deliveryDiseases of the blood and blood-forming organsRC633-647.5ENHematology, Transfusion and Cell Therapy, Vol 43, Iss , Pp S46-S53 (2021) |
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New technologies CAR cell therapies Manufacturing Gene delivery Diseases of the blood and blood-forming organs RC633-647.5 |
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New technologies CAR cell therapies Manufacturing Gene delivery Diseases of the blood and blood-forming organs RC633-647.5 Rodrigo Nalio Ramos Virginia Picanço-Castro Theo Gremen M. Oliveira Alfredo Mendrone, Junior Gil Cunha De Santis Martin Hernan Bonamino Vanderson Rocha Associação Brasileira de Hematologia, Hemoterapia e Terapia Celular Consensus on genetically modified cells. VII. Present and future of technologies for production of CAR cell therapies |
description |
Chimeric Antigen Receptor T (CAR-T) cells are certainly an important therapy for patients with relapsed and/or refractory hematologic malignancies. Currently, there are five CAR-T cell products approved by the FDA but several research groups and/or biopharmaceutical companies are encouraged to develop new products based on CAR cells using T or other cell types. Production of CAR cells requires intensive work from the basic, pre-clinical to translational levels, aiming to overcome technical difficulties and failure in the production. At least five key common steps are needed for the manipulation of T-lymphocytes (or other cells), such as: cell type selection, activation, gene delivery, cell expansion and final product formulation. However, reproducible manufacturing of high-quality clinical-grade CAR cell products is still required to apply this technology to a greater number of patients. This chapter will discuss the present and future development of new CAR designs that are safer and more effective to improve this therapy, achieving more selective killing of malignant cells and less toxicity to be applied in the clinical setting. |
format |
article |
author |
Rodrigo Nalio Ramos Virginia Picanço-Castro Theo Gremen M. Oliveira Alfredo Mendrone, Junior Gil Cunha De Santis Martin Hernan Bonamino Vanderson Rocha |
author_facet |
Rodrigo Nalio Ramos Virginia Picanço-Castro Theo Gremen M. Oliveira Alfredo Mendrone, Junior Gil Cunha De Santis Martin Hernan Bonamino Vanderson Rocha |
author_sort |
Rodrigo Nalio Ramos |
title |
Associação Brasileira de Hematologia, Hemoterapia e Terapia Celular Consensus on genetically modified cells. VII. Present and future of technologies for production of CAR cell therapies |
title_short |
Associação Brasileira de Hematologia, Hemoterapia e Terapia Celular Consensus on genetically modified cells. VII. Present and future of technologies for production of CAR cell therapies |
title_full |
Associação Brasileira de Hematologia, Hemoterapia e Terapia Celular Consensus on genetically modified cells. VII. Present and future of technologies for production of CAR cell therapies |
title_fullStr |
Associação Brasileira de Hematologia, Hemoterapia e Terapia Celular Consensus on genetically modified cells. VII. Present and future of technologies for production of CAR cell therapies |
title_full_unstemmed |
Associação Brasileira de Hematologia, Hemoterapia e Terapia Celular Consensus on genetically modified cells. VII. Present and future of technologies for production of CAR cell therapies |
title_sort |
associação brasileira de hematologia, hemoterapia e terapia celular consensus on genetically modified cells. vii. present and future of technologies for production of car cell therapies |
publisher |
Elsevier |
publishDate |
2021 |
url |
https://doaj.org/article/558a6b96477e4bcba2af415589f2cdde |
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