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A bioreactor system for the manufacture of a genetically modified Plasmodium falciparum blood stage malaria cell bank for use in a clinical trial

BACKGROUND: Although the use of induced blood stage malaria infection has proven to be a valuable tool for testing the efficacy of vaccines and drugs against Plasmodium falciparum, a limiting factor has been the availability of Good Manufacturing Practice (GMP)—compliant defined P. falciparum strain...

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Autores principales: Pawliw, Rebecca, Farrow, Rebecca, Sekuloski, Silvana, Jennings, Helen, Healer, Julie, Phuong, Thuan, Sathe, Pri, Pasay, Cielo, Evans, Krystal, Cowman, Alan F., Schofield, Louis, Chen, Nanhua, McCarthy, James, Trenholme, Katharine
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6080485/
https://www.ncbi.nlm.nih.gov/pubmed/30081913
http://dx.doi.org/10.1186/s12936-018-2435-x
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author Pawliw, Rebecca
Farrow, Rebecca
Sekuloski, Silvana
Jennings, Helen
Healer, Julie
Phuong, Thuan
Sathe, Pri
Pasay, Cielo
Evans, Krystal
Cowman, Alan F.
Schofield, Louis
Chen, Nanhua
McCarthy, James
Trenholme, Katharine
author_facet Pawliw, Rebecca
Farrow, Rebecca
Sekuloski, Silvana
Jennings, Helen
Healer, Julie
Phuong, Thuan
Sathe, Pri
Pasay, Cielo
Evans, Krystal
Cowman, Alan F.
Schofield, Louis
Chen, Nanhua
McCarthy, James
Trenholme, Katharine
author_sort Pawliw, Rebecca
collection PubMed
description BACKGROUND: Although the use of induced blood stage malaria infection has proven to be a valuable tool for testing the efficacy of vaccines and drugs against Plasmodium falciparum, a limiting factor has been the availability of Good Manufacturing Practice (GMP)—compliant defined P. falciparum strains for in vivo use. The aim of this study was to develop a cost-effective method for the large-scale production of P. falciparum cell banks suitable for use in clinical trials. METHODS: Genetically-attenuated parasites (GAP) were produced by targeted deletion of the gene encoding the knob associated histidine rich protein (kahrp) from P. falciparum strain 3D7. A GAP master cell bank (MCB) was manufactured by culturing parasites in an FDA approved single use, closed system sterile plastic bioreactor. All components used to manufacture the MCB were screened to comply with standards appropriate for in vivo use. The cryopreserved MCB was subjected to extensive testing to ensure GMP compliance for a phase 1 investigational product. RESULTS: Two hundred vials of the GAP MCB were successfully manufactured. At harvest, the GAP MCB had a parasitaemia of 6.3%, with 96% of parasites at ring stage. Testing confirmed that all release criteria were met (sterility, absence of viral contaminants and endotoxins, parasite viability following cryopreservation, identity and anti-malarial drug sensitivity of parasites). CONCLUSION: Large-scale in vitro culture of P. falciparum parasites using a wave bioreactor can be achieved under GMP-compliant conditions. This provides a cost-effective methodology for the production of malaria parasites suitable for administration in clinical trials.
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spelling pubmed-60804852018-08-09 A bioreactor system for the manufacture of a genetically modified Plasmodium falciparum blood stage malaria cell bank for use in a clinical trial Pawliw, Rebecca Farrow, Rebecca Sekuloski, Silvana Jennings, Helen Healer, Julie Phuong, Thuan Sathe, Pri Pasay, Cielo Evans, Krystal Cowman, Alan F. Schofield, Louis Chen, Nanhua McCarthy, James Trenholme, Katharine Malar J Methodology BACKGROUND: Although the use of induced blood stage malaria infection has proven to be a valuable tool for testing the efficacy of vaccines and drugs against Plasmodium falciparum, a limiting factor has been the availability of Good Manufacturing Practice (GMP)—compliant defined P. falciparum strains for in vivo use. The aim of this study was to develop a cost-effective method for the large-scale production of P. falciparum cell banks suitable for use in clinical trials. METHODS: Genetically-attenuated parasites (GAP) were produced by targeted deletion of the gene encoding the knob associated histidine rich protein (kahrp) from P. falciparum strain 3D7. A GAP master cell bank (MCB) was manufactured by culturing parasites in an FDA approved single use, closed system sterile plastic bioreactor. All components used to manufacture the MCB were screened to comply with standards appropriate for in vivo use. The cryopreserved MCB was subjected to extensive testing to ensure GMP compliance for a phase 1 investigational product. RESULTS: Two hundred vials of the GAP MCB were successfully manufactured. At harvest, the GAP MCB had a parasitaemia of 6.3%, with 96% of parasites at ring stage. Testing confirmed that all release criteria were met (sterility, absence of viral contaminants and endotoxins, parasite viability following cryopreservation, identity and anti-malarial drug sensitivity of parasites). CONCLUSION: Large-scale in vitro culture of P. falciparum parasites using a wave bioreactor can be achieved under GMP-compliant conditions. This provides a cost-effective methodology for the production of malaria parasites suitable for administration in clinical trials. BioMed Central 2018-08-06 /pmc/articles/PMC6080485/ /pubmed/30081913 http://dx.doi.org/10.1186/s12936-018-2435-x Text en © The Author(s) 2018 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Methodology
Pawliw, Rebecca
Farrow, Rebecca
Sekuloski, Silvana
Jennings, Helen
Healer, Julie
Phuong, Thuan
Sathe, Pri
Pasay, Cielo
Evans, Krystal
Cowman, Alan F.
Schofield, Louis
Chen, Nanhua
McCarthy, James
Trenholme, Katharine
A bioreactor system for the manufacture of a genetically modified Plasmodium falciparum blood stage malaria cell bank for use in a clinical trial
title A bioreactor system for the manufacture of a genetically modified Plasmodium falciparum blood stage malaria cell bank for use in a clinical trial
title_full A bioreactor system for the manufacture of a genetically modified Plasmodium falciparum blood stage malaria cell bank for use in a clinical trial
title_fullStr A bioreactor system for the manufacture of a genetically modified Plasmodium falciparum blood stage malaria cell bank for use in a clinical trial
title_full_unstemmed A bioreactor system for the manufacture of a genetically modified Plasmodium falciparum blood stage malaria cell bank for use in a clinical trial
title_short A bioreactor system for the manufacture of a genetically modified Plasmodium falciparum blood stage malaria cell bank for use in a clinical trial
title_sort bioreactor system for the manufacture of a genetically modified plasmodium falciparum blood stage malaria cell bank for use in a clinical trial
topic Methodology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6080485/
https://www.ncbi.nlm.nih.gov/pubmed/30081913
http://dx.doi.org/10.1186/s12936-018-2435-x
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