Evidence map›Paper›PMID 28588308›Full record

ArticleScientific reports2017

A Four-Biomarker Blood Signature Discriminates Systemic Inflammation Due to Viral Infection Versus Other Etiologies.

D L Sampson, B A Fox, T D Yager, S Bhide, S Cermelli, L C McHugh, T A Seldon, R A Brandon, E Sullivan, J J Zimmerman and 2 more

Abstract read
In one paragraph

Article in Scientific reports, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 45 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
45citing papers in PubMed, 1 pooled it
–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

45 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
  2. Review
  3. Review
  4. Article
  5. Article
  6. AnViruses · 2025
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  12. Immunomodulatory activity of heat-killedFood science & nutrition · 2024
    Article
  13. Sepsis heterogeneity.World journal of pediatrics : WJP · 2023
    Review
  14. Article
  15. Article
  16. Article
  17. Article
  18. Article
  19. Cytokine Storm-Definition, Causes, and Implications.International journal of molecular sciences · 2022
    Review
  20. 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

12 authors.

D L SampsonImmunexpress Inc., Seattle, WA, 98109, USA.
B A FoxImmunexpress Inc., Seattle, WA, 98109, USA.
T D YagerImmunexpress Inc., Seattle, WA, 98109, USA.
S BhideImmunexpress Inc., Seattle, WA, 98109, USA.
S CermelliImmunexpress Inc., Seattle, WA, 98109, USA.
L C McHughImmunexpress Inc., Seattle, WA, 98109, USA.
T A SeldonImmunexpress Inc., Seattle, WA, 98109, USA.
R A BrandonImmunexpress Inc., Seattle, WA, 98109, USA.
E SullivanDivision of Pediatric Critical Care Medicine, Seattle Children's Hospital, Seattle, WA, 98105, USA.
J J ZimmermanDivision of Pediatric Critical Care Medicine, Seattle Children's Hospital, Seattle, WA, 98105, USA.
M NoursadeghiDivision of Infection & Immunity, University College London, Cruciform Building, 90 Gower Street, London, WC1E 6BT, United Kingdom.
R B BrandonImmunexpress Inc., Seattle, WA, 98109, USA. richard.b@immunexpress.com.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The innate immune system of humans and other mammals responds to pathogen-associated molecular patterns (PAMPs) that are conserved across broad classes of infectious agents such as bacteria and viruses. We hypothesized that a blood-based transcriptional signature could be discovered indicating a host systemic response to viral infection. Previous work identified host transcriptional signatures to individual viruses including influenza, respiratory syncytial virus and dengue, but the generality of these signatures across all viral infection types has not been established. Based on 44 publicly available datasets and two clinical studies of our own design, we discovered and validated a four-gene expression signature in whole blood, indicative of a general host systemic response to many types of viral infection. The signature's genes are: Interferon Stimulated Gene 15 (ISG15), Interleukin 16 (IL16), 2',5'-Oligoadenylate Synthetase Like (OASL), and Adhesion G Protein Coupled Receptor E5 (ADGRE5). In each of 13 validation datasets encompassing human, macaque, chimpanzee, pig, mouse, rat and all seven Baltimore virus classification groups, the signature provides statistically significant (p < 0.05) discrimination between viral and non-viral conditions. The signature may have clinical utility for differentiating host systemic inflammation (SI) due to viral versus bacterial or non-infectious causes.

Indexed as

BiomarkersAdolescentCase-Control StudiesChildChild, PreschoolDatabases, FactualFemaleGene Expression ProfilingHost-Pathogen InteractionsHumansInfantInflammationMaleReproducibility of ResultsTranscriptomeVirus DiseasesBiomarkers

Identifiers

PMID28588308
PMCPMC5460227

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.