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Journal article

Chimpanzee adenoviral vectors as vaccines for outbreak pathogens

Abstract:
The 2014-15 Ebola outbreak in West Africa highlighted the potential for large disease outbreaks caused by emerging pathogens and has generated considerable focus on preparedness for future epidemics. Here we discuss drivers, strategies and practical considerations for developing vaccines against outbreak pathogens. Chimpanzee adenoviral (ChAd) vectors have been developed as vaccine candidates for multiple infectious diseases and prostate cancer. ChAd vectors are safe and induce antigen-specific cellular and humoral immunity in all age groups, as well as circumventing the problem of pre-existing immunity encountered with human Ad vectors. For these reasons, such viral vectors provide an attractive platform for stockpiling vaccines for emergency deployment in response to a threatened outbreak of an emerging pathogen. Work is already underway to develop vaccines against a number of other outbreak pathogens and we will also review progress on these approaches here, particularly for Lassa fever, Nipah and MERS.
Publication status:
Published
Peer review status:
Peer reviewed

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Publisher copy:
10.1080/21645515.2017.1383575

Authors


More by this author
Institution:
University of Oxford
Division:
MSD
Department:
NDM
Sub department:
Jenner Institute
Role:
Author
More by this author
Institution:
University of Oxford
Division:
MSD
Department:
NDM
Sub department:
Jenner Institute
Role:
Author
More by this author
Institution:
University of Oxford
Division:
MSD
Department:
NDM
Sub department:
Jenner Institute
Role:
Author
More by this author
Institution:
University of Oxford
Division:
MSD
Department:
NDM
Sub department:
Jenner Institute
Role:
Author
More by this author
Institution:
University of Oxford
Division:
MSD
Department:
NDM
Sub department:
Jenner Institute
Role:
Author


Publisher:
Taylor and Francis
Journal:
Human Vaccines and Immunotherapeutics More from this journal
Volume:
13
Issue:
12: The International Society for Vaccines 2016 Annual
Pages:
3020-3032
Publication date:
2017-10-30
Acceptance date:
2017-09-19
DOI:
EISSN:
2164-554X
ISSN:
2164-5515


Pubs id:
pubs:729302
UUID:
uuid:1a9d62f3-5d24-4feb-bd87-973a2143baa5
Local pid:
pubs:729302
Source identifiers:
729302
Deposit date:
2017-09-19

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