Evidence map›Paper›PMID 37747758›Full record

ArticleBiotechnology and bioengineering2024

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

Carina C D Joe, Rameswara R Segireddy, Cathy Oliveira, Adam Berg, Yuanyuan Li, Dimitrios Doultsinos, Steffi Scholze, Asma Ahmad, Piergiuseppe Nestola, Julia Niemann and 1 more

Open access · hybridAbstract read
In one paragraph

Article in Biotechnology and bioengineering, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
3.4field-weighted citation impact, top 7% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

10 citing papers in PubMed, 11 citations in OpenAlex.

  1. Trial
  2. Article
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  4. Article
  5. Article
  6. Developing the next-generation of adenoviral vector vaccines.Human vaccines & immunotherapeutics · 2025
    Review
  7. Review
  8. Article
  9. Article
  10. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

11 authors at 4 institutions in 3 countries.

Carina C D JoeJenner Institute, Nuffield Department of Medicine, University of Oxford, Oxford, UK.
Rameswara R SegireddyJenner Institute, Nuffield Department of Medicine, University of Oxford, Oxford, UK.
Cathy OliveiraClinical Biomanufacturing Facility, Nuffield Department of Medicine, University of Oxford, Oxford, UK.
Adam BergJenner Institute, Nuffield Department of Medicine, University of Oxford, Oxford, UK.
Yuanyuan LiJenner Institute, Nuffield Department of Medicine, University of Oxford, Oxford, UK.
Dimitrios DoultsinosJenner Institute, Nuffield Department of Medicine, University of Oxford, Oxford, UK.
Steffi ScholzeSartorius Stedim Biotech GmbH, Goettingen, Germany.
Asma AhmadRepligen Corporation, Waltham, Massachusetts, USA.
Piergiuseppe NestolaSartorius Stedim Biotech GmbH, Goettingen, Germany.
Julia NiemannSartorius Stedim Biotech GmbH, Goettingen, Germany.
Alexander D DouglasJenner Institute, Nuffield Department of Medicine, University of Oxford, Oxford, UK.ORCID 0000-0002-5410-7562
University of Oxford · GBSartorius (Germany) · DEJohn Radcliffe Hospital · GBRepligen (United States) · US

Funding

Wellcome TrustWellcome Trust 220679/Z/20/Z
6 · The paper itself

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.

Indexed as

AdenoviridaeAdenovirus VaccinesBioreactorsChAdOx1 nCoV-19Disease OutbreaksHumansAdenovirus VaccinesChAdOx1 nCoV-19adenovirusemergency responseoutbreak responsepandemic responseperfusionviral-vector vaccine

Identifiers

PMID37747758
PMCPMC10932548
OpenAlexW4387002094

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.