Evidence map›Paper›PMID 28576573›Full record

ReviewVaccine2017

Rapid development of vaccines against emerging pathogens: The replication-deficient simian adenovirus platform technology.

Sarah C Gilbert, George M Warimwe

Open access · hybridAbstract readReview
In one paragraph

Review in Vaccine, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
2.6field-weighted citation impact, top 11% 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

19 citing papers in PubMed, 33 citations in OpenAlex.

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  12. Emerging viruses and current strategies for vaccine intervention.Clinical and experimental immunology · 2019
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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

2 authors at 1 institution in 2 countries.

Sarah C GilbertThe Jenner Institute, University of Oxford, Old Road Campus Research Building, Roosevelt Drive, Oxford OX3 7DQ, United Kingdom. Electronic address: sarah.gilbert@ndm.ox.ac.uk.
George M WarimweThe Jenner Institute, University of Oxford, Old Road Campus Research Building, Roosevelt Drive, Oxford OX3 7DQ, United Kingdom; Kenya Medical Research Institute-Wellcome Trust Research Programme, P.O. Box 230-80108, Kilifi, Kenya; The Pirbright Institute, Woking GU24 0NF, United Kingdom.
University of Oxford · GB

Funding

Wellcome Trust
6 · The paper itself

Abstract

Despite the fact that there had been multiple small outbreaks of Ebola Virus Disease, when a large outbreak occurred in 2014 there were no vaccines or drugs available for use. Clinical development of multiple candidate vaccines was then initiated in parallel with attempts to contain the outbreak but only one vaccine was eventually tested in a phase III trial. In order to be better prepared for future outbreaks of known human pathogens, platform technologies to accelerate vaccine development should be employed, allowing vaccine developers to take advantage of detailed knowledge of the vaccine platform and facilitating rapid progress to clinical trials and eventually to vaccine stockpiles. This review gives an example of one such vaccine platform, replication-deficient simian adenoviruses, and describes progress in human and livestock vaccine development for three outbreak pathogens, Ebola virus, Rift Valley Fever Virus and Middle East Respiratory Syndrome Coronavirus.

Indexed as

Adenoviruses, SimianAfricaAnimalsClinical Trials as TopicCommunicable Diseases, EmergingCoronavirus InfectionsDisease OutbreaksEbolavirusGenetic VectorsHemorrhagic Fever, EbolaHumansMiddle East Respiratory Syndrome CoronavirusRift Valley FeverRift Valley fever virusViral VaccinesVirus ReplicationViral VaccinesClinical trialsOutbreak pathogenSimian adenoviral vectorVaccination

Identifiers

PMID28576573
PMCPMC5571606
OpenAlexW2620232732

What OpenQuestion holds

Textmetadata
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.