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Transient transfection of serum-free suspension HEK 293 cell culture for efficient production of human rFVIII

BACKGROUND: Hemophilia A is a bleeding disorder caused by deficiency in coagulation factor VIII. Recombinant factor VIII (rFVIII) is an alternative to plasma-derived FVIII for the treatment of hemophilia A. However, commercial manufacturing of rFVIII products is inefficient and costly and is associa...

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Autores principales: Swiech, Kamilla, Kamen, Amine, Ansorge, Sven, Durocher, Yves, Picanço-Castro, Virgínia, Russo-Carbolante, Elisa MS, Neto, Mário SA, Covas, Dimas T
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3254136/
https://www.ncbi.nlm.nih.gov/pubmed/22115125
http://dx.doi.org/10.1186/1472-6750-11-114
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author Swiech, Kamilla
Kamen, Amine
Ansorge, Sven
Durocher, Yves
Picanço-Castro, Virgínia
Russo-Carbolante, Elisa MS
Neto, Mário SA
Covas, Dimas T
author_facet Swiech, Kamilla
Kamen, Amine
Ansorge, Sven
Durocher, Yves
Picanço-Castro, Virgínia
Russo-Carbolante, Elisa MS
Neto, Mário SA
Covas, Dimas T
author_sort Swiech, Kamilla
collection PubMed
description BACKGROUND: Hemophilia A is a bleeding disorder caused by deficiency in coagulation factor VIII. Recombinant factor VIII (rFVIII) is an alternative to plasma-derived FVIII for the treatment of hemophilia A. However, commercial manufacturing of rFVIII products is inefficient and costly and is associated to high prices and product shortage, even in economically privileged countries. This situation may be solved by adopting more efficient production methods. Here, we evaluated the potential of transient transfection in producing rFVIII in serum-free suspension HEK 293 cell cultures and investigated the effects of different DNA concentration (0.4, 0.6 and 0.8 μg/10(6 )cells) and repeated transfections done at 34° and 37°C. RESULTS: We observed a decrease in cell growth when high DNA concentrations were used, but no significant differences in transfection efficiency and in the biological activity of the rFVIII were noticed. The best condition for rFVIII production was obtained with repeated transfections at 34°C using 0.4 μg DNA/10(6 )cells through which almost 50 IU of active rFVIII was produced six days post-transfection. CONCLUSION: Serum-free suspension transient transfection is thus a viable option for high-yield-rFVIII production. Work is in progress to further optimize the process and validate its scalability.
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spelling pubmed-32541362012-01-11 Transient transfection of serum-free suspension HEK 293 cell culture for efficient production of human rFVIII Swiech, Kamilla Kamen, Amine Ansorge, Sven Durocher, Yves Picanço-Castro, Virgínia Russo-Carbolante, Elisa MS Neto, Mário SA Covas, Dimas T BMC Biotechnol Research Article BACKGROUND: Hemophilia A is a bleeding disorder caused by deficiency in coagulation factor VIII. Recombinant factor VIII (rFVIII) is an alternative to plasma-derived FVIII for the treatment of hemophilia A. However, commercial manufacturing of rFVIII products is inefficient and costly and is associated to high prices and product shortage, even in economically privileged countries. This situation may be solved by adopting more efficient production methods. Here, we evaluated the potential of transient transfection in producing rFVIII in serum-free suspension HEK 293 cell cultures and investigated the effects of different DNA concentration (0.4, 0.6 and 0.8 μg/10(6 )cells) and repeated transfections done at 34° and 37°C. RESULTS: We observed a decrease in cell growth when high DNA concentrations were used, but no significant differences in transfection efficiency and in the biological activity of the rFVIII were noticed. The best condition for rFVIII production was obtained with repeated transfections at 34°C using 0.4 μg DNA/10(6 )cells through which almost 50 IU of active rFVIII was produced six days post-transfection. CONCLUSION: Serum-free suspension transient transfection is thus a viable option for high-yield-rFVIII production. Work is in progress to further optimize the process and validate its scalability. BioMed Central 2011-11-24 /pmc/articles/PMC3254136/ /pubmed/22115125 http://dx.doi.org/10.1186/1472-6750-11-114 Text en Copyright ©2011 Swiech et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Swiech, Kamilla
Kamen, Amine
Ansorge, Sven
Durocher, Yves
Picanço-Castro, Virgínia
Russo-Carbolante, Elisa MS
Neto, Mário SA
Covas, Dimas T
Transient transfection of serum-free suspension HEK 293 cell culture for efficient production of human rFVIII
title Transient transfection of serum-free suspension HEK 293 cell culture for efficient production of human rFVIII
title_full Transient transfection of serum-free suspension HEK 293 cell culture for efficient production of human rFVIII
title_fullStr Transient transfection of serum-free suspension HEK 293 cell culture for efficient production of human rFVIII
title_full_unstemmed Transient transfection of serum-free suspension HEK 293 cell culture for efficient production of human rFVIII
title_short Transient transfection of serum-free suspension HEK 293 cell culture for efficient production of human rFVIII
title_sort transient transfection of serum-free suspension hek 293 cell culture for efficient production of human rfviii
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3254136/
https://www.ncbi.nlm.nih.gov/pubmed/22115125
http://dx.doi.org/10.1186/1472-6750-11-114
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