Evidence map›Paper›PMID 22110166›Full record

Trial reportThe Journal of experimental medicine2011

A genomic storm in critically injured humans.

Wenzhong Xiao, Michael N Mindrinos, Junhee Seok, Joseph Cuschieri, Alex G Cuenca, Hong Gao, Douglas L Hayden, Laura Hennessy, Ernest E Moore, Joseph P Minei and 31 more

4 registry-linked trialsAbstract readClinical TrialMulticenter Study
In one paragraph

Trial report in The Journal of experimental medicine, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to 4 registered trials, which are not on this map. Cited by 596 papers, 3 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
596citing papers in PubMed, 3 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.

NCT00257231 completednot on this map

Inflammation and the Host Response to Injury

TypeobservationalSponsorMassachusetts General HospitalRan2003 to 2018Enrolled610ConditionsTrauma, Burns, Multiple Organ Failure
NCT00257244 completednot on this map

Inflammation and the Host Response to Injury

TypeobservationalSponsorMassachusetts General HospitalRan2004 to 2018Enrolled280ConditionsTrauma, Burns, Multiple Organ Failure
NCT03671746 phase1completednot on this mapstarted 2019, after this paper: background citation

Inflammatory Response to Trauma - Does Early Cytokine Modulation Improve Patient Outcome

TypeinterventionalSponsorArun AnejaRan2019 to 2023Enrolled70ConditionsPolytraumaArmsKetorolac, Saline Solution
NCT04693442 unknown statusnot on this mapstarted 2016, after this paper: background citation

A Multi-centre, Prospective Study to Examine the Relationship Between Neutrophil Function and Sepsis in Adults and Children With Severe Thermal Injuries

TypeobservationalSponsorUniversity Hospital Birmingham NHS Foundation TrustRan2016 to 2022Enrolled245ConditionsBurnsArmstaking of blood, urine and blood samples and objective scar assessment
3 · Its place in the literature

Who cites it

596 citing papers in PubMed, 3 syntheses or guidelines pooled it.

  1. Neutrophil cell surface receptor dynamics following trauma: a systematic review.European journal of trauma and emergency surgery : official publication of the European Trauma Society · 2025
    Pooled it
  2. Pooled it
  3. Pooled it
  4. Trial
  5. Trial
  6. Trial
  7. Trial
  8. Trial
  9. Article
  10. Review
  11. Wound Healing Potential of Selenium and Nanoselenium.Biological trace element research · 2026
    Review
  12. Article
  13. Article
  14. Article
  15. Article
  16. Review
  17. Review
  18. Inflammatory Stewardship-A Perspective for Active Management of Acute Inflammation.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2026
    Article
  19. Article
  20. Article

536 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

41 authors.

Wenzhong XiaoDepartment of Surgery, Massachusetts General Hospital, Harvard Medical School, Boston, MA 02114, USA.
Michael N Mindrinos
Junhee Seok
Joseph Cuschieri
Alex G Cuenca
Hong Gao
Douglas L Hayden
Laura Hennessy
Ernest E Moore
Joseph P Minei
Paul E Bankey
Jeffrey L Johnson
Jason Sperry
Avery B Nathens
Timothy R Billiar
Michael A West
Bernard H Brownstein
Philip H Mason
Henry V Baker
Celeste C Finnerty
Marc G Jeschke
M Cecilia López
Matthew B Klein
Richard L Gamelli
Nicole S Gibran
Brett Arnoldo
Weihong Xu
Yuping Zhang
Steven E Calvano
Grace P McDonald-Smith
David A Schoenfeld
John D Storey
J Perren Cobb
H Shaw Warren
Lyle L Moldawer
David N Herndon
Stephen F Lowry
Ronald V Maier
Ronald W Davis
Ronald G Tompkins
Inflammation and Host Response to Injury Large-Scale Collaborative Research Program

Funding

Inflammation and the Response to InjuryU54GM062119 · NIGMS · MASSACHUSETTS GENERAL HOSPITAL · PI TOMPKINS, RONALD GARY · 2001 to 2010
$78.6M
University of Pittsburgh Clinical and Translational Science InstitutionKL2TR000146 · NCATS · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI REIS, STEVEN E · 2012 to 2015
$8.7M
Molecular Biology in Burns and TraumaT32GM008721 · NIGMS · UNIVERSITY OF FLORIDA · PI Philip A Efron · 1999 to 2026
$5.0M
Interruption of Signaling-Mediated Bacterial Persistent InfectionsR33AI105902 · NIAID · MASSACHUSETTS GENERAL HOSPITAL · PI RAHME, LAURENCE G · 2015 to 2017
$1.8M
NCATS NIH HHS KL2 TR000146NIAID NIH HHS R33 AI105902NIGMS NIH HHS 5U54 GM-062119-10NIGMS NIH HHS T32 GM008721NIGMS NIH HHS U54 GM062119
6 · The paper itself

Abstract

Human survival from injury requires an appropriate inflammatory and immune response. We describe the circulating leukocyte transcriptome after severe trauma and burn injury, as well as in healthy subjects receiving low-dose bacterial endotoxin, and show that these severe stresses produce a global reprioritization affecting >80% of the cellular functions and pathways, a truly unexpected "genomic storm." In severe blunt trauma, the early leukocyte genomic response is consistent with simultaneously increased expression of genes involved in the systemic inflammatory, innate immune, and compensatory antiinflammatory responses, as well as in the suppression of genes involved in adaptive immunity. Furthermore, complications like nosocomial infections and organ failure are not associated with any genomic evidence of a second hit and differ only in the magnitude and duration of this genomic reprioritization. The similarities in gene expression patterns between different injuries reveal an apparently fundamental human response to severe inflammatory stress, with genomic signatures that are surprisingly far more common than different. Based on these transcriptional data, we propose a new paradigm for the human immunological response to severe injury.

Indexed as

Gene Expression RegulationGenome, HumanTranscription, GeneticAdaptive ImmunityAdultBurnsCritical IllnessEndotoxinsFemaleHumansImmunity, InnateInflammationLeukocytesMaleTrauma Severity IndicesEndotoxins

Identifiers

PMID22110166
PMCPMC3244029

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-SA
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Registered trials

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.