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Accelerated and intensified manufacturing of an adenovirus-vectored vaccine to enable rapid outbreak response.
Joe, Carina C D; Segireddy, Rameswara R; Oliveira, Cathy; Berg, Adam; Li, Yuanyuan; Doultsinos, Dimitrios; Scholze, Steffi; Ahmad, Asma; Nestola, Piergiuseppe; Niemann, Julia; Douglas, Alexander D.
Afiliação
  • Joe CCD; Jenner Institute, Nuffield Department of Medicine, University of Oxford, Oxford, UK.
  • Segireddy RR; Jenner Institute, Nuffield Department of Medicine, University of Oxford, Oxford, UK.
  • Oliveira C; Clinical Biomanufacturing Facility, Nuffield Department of Medicine, University of Oxford, Oxford, UK.
  • Berg A; Jenner Institute, Nuffield Department of Medicine, University of Oxford, Oxford, UK.
  • Li Y; Jenner Institute, Nuffield Department of Medicine, University of Oxford, Oxford, UK.
  • Doultsinos D; Jenner Institute, Nuffield Department of Medicine, University of Oxford, Oxford, UK.
  • Scholze S; Nuffield Department of Surgical Sciences, John Radcliffe Hospital, University of Oxford, Oxford, UK.
  • Ahmad A; Sartorius Stedim Biotech GmbH, Goettingen, Germany.
  • Nestola P; Repligen Corporation, Waltham, Massachusetts, USA.
  • Niemann J; Sartorius Stedim Biotech GmbH, Goettingen, Germany.
  • Douglas AD; Sartorius Stedim Biotech GmbH, Goettingen, Germany.
Biotechnol Bioeng ; 121(1): 176-191, 2024 01.
Article em En | MEDLINE | ID: mdl-37747758
The Coalition for Epidemic Preparedness Innovations' "100-day moonshot" aspires to launch a new vaccine within 100 days of pathogen identification, followed by large-scale vaccine availability within the "second hundred days." Here, we describe work to optimize adenoviral vector manufacturing for rapid response, by minimizing time to clinical trial and first large-scale supply, and maximizing output from the available manufacturing footprint. We describe a rapid virus seed expansion workflow that allows vaccine release to clinical trials within 60 days of antigen sequence identification, followed by vaccine release from globally distributed sites within a further 40 days. We also describe a perfusion-based upstream production process, designed to maximize output while retaining simplicity and suitability for existing manufacturing facilities. This improves upstream volumetric productivity of ChAdOx1 nCoV-19 by approximately fourfold and remains compatible with the existing downstream process, yielding drug substance sufficient for 10,000 doses from each liter of bioreactor capacity. This accelerated manufacturing process, along with other advantages such as thermal stability, supports the ongoing value of adenovirus-vectored vaccines as a rapidly adaptable and deployable platform for emergency response.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Adenoviridae / Vacinas contra Adenovirus Limite: Humans Idioma: En Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Adenoviridae / Vacinas contra Adenovirus Limite: Humans Idioma: En Ano de publicação: 2024 Tipo de documento: Article