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Accelerated and intensified manufacturing of an adenovirus-vectored vaccine to enable rapid outbreak response.

Authors
  • Joe, Carina C D1
  • Segireddy, Rameswara R1
  • Oliveira, Cathy2
  • Berg, Adam1
  • Li, Yuanyuan1
  • Doultsinos, Dimitrios1, 3
  • Scholze, Steffi4
  • Ahmad, Asma5
  • Nestola, Piergiuseppe4
  • Niemann, Julia4
  • Douglas, Alexander D1
  • 1 Jenner Institute, Nuffield Department of Medicine, University of Oxford, Oxford, UK.
  • 2 Clinical Biomanufacturing Facility, Nuffield Department of Medicine, University of Oxford, Oxford, UK. , (Oman)
  • 3 Nuffield Department of Surgical Sciences, John Radcliffe Hospital, University of Oxford, Oxford, UK.
  • 4 Sartorius Stedim Biotech GmbH, Goettingen, Germany. , (Germany)
  • 5 Repligen Corporation, Waltham, Massachusetts, USA.
Type
Published Article
Journal
Biotechnology and Bioengineering
Publisher
Wiley (John Wiley & Sons)
Publication Date
Jan 01, 2024
Volume
121
Issue
1
Pages
176–191
Identifiers
DOI: 10.1002/bit.28553
PMID: 37747758
Source
Medline
Keywords
Language
English
License
Unknown

Abstract

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. © 2023 The Authors. Biotechnology and Bioengineering published by Wiley Periodicals LLC.

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