Evidence map›Paper›PMID 28128003›Full record

ReviewFuture medicinal chemistry2017

Current and future developments in the treatment of virus-induced hypercytokinemia.

Jonathan P Wong, Satya Viswanathan, Ming Wang, Lun-Quan Sun, Graeme C Clark, Riccardo V D'Elia

Abstract readReview
In one paragraph

Review in Future medicinal chemistry, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 46 papers.

0numbers the graph read from it
0cells of the map it votes in
46citing papers in PubMed
–field-weighted citation impact
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

46 citing papers in PubMed.

  1. Trial
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  3. Journal of thoracic disease · 2026
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  7. Review
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  9. Novel Substituted Azoloazines with Anticoagulant Activity.International journal of molecular sciences · 2023
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  14. Observational
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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

6 authors.

Jonathan P WongDefence Research & Development Canada, Suffield Research Centre, Ralston, Alberta, Canada.
Satya ViswanathanDefence Research & Development Canada, Suffield Research Centre, Ralston, Alberta, Canada.
Ming WangCollege of Veterinary Medicine, China Agriculture University, Beijing, China.
Lun-Quan SunCenter for Molecular Medicine, Xiangya Hospital, Central South University, Changsa, China.
Graeme C ClarkCBR Division, Defence Science & Technology Laboratory, Porton Down, Salisbury, UK.
Riccardo V D'EliaCBR Division, Defence Science & Technology Laboratory, Porton Down, Salisbury, UK.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Emerging pathogenic viruses such as Ebola and Middle Eastern Respiratory Syndrome coronavirus (MERS-CoV) can cause acute infections through the evasion of the host's antiviral immune responses and by inducing the upregulation of inflammatory cytokines. This immune dysregulation, termed a cytokine storm or hypercytokinemia, is potentially fatal and is a significant underlying factor in increased mortality of infected patients. The prevalence of global outbreaks in recent years has offered opportunities to study the progression of various viral infections and have provided an improved understanding of hypercytokinemia associated with these diseases. However, despite this increased knowledge and the study of the infections caused by a range of emerging viruses, the therapeutic options still remain limited. This review aims to explore alternative experimental strategies for treating hypercytokinemia induced by the Ebola, avian influenza and Dengue viruses; outlining their modes of action, summarizing their preclinical assessments and potential clinical applications.

Indexed as

AnimalsAntiviral AgentsBirdsCytokinesDengueHemorrhagic Fever, EbolaHumansInflammationInfluenza in BirdsAntiviral AgentsCytokinesemerging viruseshypercytokinemiatreatment

Identifiers

PMID28128003
PMCPMC7079716

What OpenQuestion holds

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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.