Evidence map›Paper›PMID 24956170›Full record

ArticlePloS one2014

S100A8/A9 mRNA induction in an ex vivo model of endotoxin tolerance: roles of IL-10 and IFNγ.

Mathieu Fontaine, Séverine Planel, Estelle Peronnet, Fanny Turrel-Davin, Vincent Piriou, Alexandre Pachot, Guillaume Monneret, Alain Lepape, Fabienne Venet

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed, 1 pooled it
1.6field-weighted citation impact, top 18% 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

20 citing papers in PubMed, 1 synthesis or guideline pooled it, 34 citations in OpenAlex.

  1. Pooled it
  2. Review
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  5. Review
  6. Article
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  11. Prospective evaluation of S100A12 and S100A8/A9 (calprotectin) in dogs with sepsis or the systemic inflammatory response syndrome.Journal of veterinary diagnostic investigation : official publication of the American Association of Veterinary Laboratory Diagnosticians, Inc · 2019
    Article
  12. Article
  13. CD14Gut · 2018
    Article
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  15. Article
  16. Observational
  17. S100A8/A9 and sRAGE kinetic after polytrauma; an explorative observational study.Scandinavian journal of trauma, resuscitation and emergency medicine · 2017
    Observational
  18. Review
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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

9 authors at 4 institutions in 1 country.

Mathieu FontaineHospices Civils de Lyon - Intensive Care Unit, Centre Hospitalier Lyon-Sud, Pierre-Bénite, France; Joint Unit Hospices Civils de Lyon - bioMérieux, Hôpital Edouard Herriot, Lyon, France; EAM 4174 "Hemostasis, inflammation and sepsis" Hospices Civils de Lyon - Université Claude Bernard Lyon I, Lyon, France.
Séverine PlanelJoint Unit Hospices Civils de Lyon - bioMérieux, Hôpital Edouard Herriot, Lyon, France.
Estelle PeronnetJoint Unit Hospices Civils de Lyon - bioMérieux, Hôpital Edouard Herriot, Lyon, France.
Fanny Turrel-DavinJoint Unit Hospices Civils de Lyon - bioMérieux, Hôpital Edouard Herriot, Lyon, France.
Vincent PiriouHospices Civils de Lyon - Intensive Care Unit, Centre Hospitalier Lyon-Sud, Pierre-Bénite, France; EAM 4174 "Hemostasis, inflammation and sepsis" Hospices Civils de Lyon - Université Claude Bernard Lyon I, Lyon, France.
Alexandre PachotJoint Unit Hospices Civils de Lyon - bioMérieux, Hôpital Edouard Herriot, Lyon, France.
Guillaume MonneretJoint Unit Hospices Civils de Lyon - bioMérieux, Hôpital Edouard Herriot, Lyon, France; EAM 4174 "Hemostasis, inflammation and sepsis" Hospices Civils de Lyon - Université Claude Bernard Lyon I, Lyon, France; Hospices Civils de Lyon - Immunology Laboratory, Hôpital Edouard Herriot, Lyon, France.
Alain LepapeHospices Civils de Lyon - Intensive Care Unit, Centre Hospitalier Lyon-Sud, Pierre-Bénite, France; Joint Unit Hospices Civils de Lyon - bioMérieux, Hôpital Edouard Herriot, Lyon, France; EAM 4174 "Hemostasis, inflammation and sepsis" Hospices Civils de Lyon - Université Claude Bernard Lyon I, Lyon, France.
Fabienne VenetJoint Unit Hospices Civils de Lyon - bioMérieux, Hôpital Edouard Herriot, Lyon, France; EAM 4174 "Hemostasis, inflammation and sepsis" Hospices Civils de Lyon - Université Claude Bernard Lyon I, Lyon, France; Hospices Civils de Lyon - Immunology Laboratory, Hôpital Edouard Herriot, Lyon, France.
bioMérieux (France) · FRHôpital Edouard Herriot · FRHôpital Lyon Sud · FRHospices Civils de Lyon · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectivesSeptic syndromes are the leading cause of death in intensive care units. They are characterized by the development of immune dysfunctions such as endotoxin tolerance (ET), whose intensity and duration are associated with increased risk of nosocomial infections and mortality. Alarmins S100A8 and S100A9 have been shown to be increased after septic shock. Importantly, a delayed S100A9 mRNA increase predicts hospital-acquired infection in patients. The aim of this study was to investigate the regulation of S100A8 and S100A9 mRNA expression in an ex vivo model of ET. SUBJECTS AND MEASUREMENTS: ET was reproduced ex vivo by priming healthy peripheral blood mononuclear cells (number of donors  = 9 to 10) with low-dose endotoxin (2 ng/ml) before stimulation with high dose endotoxin (100 ng/ml). S100A8 and S100A9 mRNA levels were measured by quantitative real-time polymerase chain reactions. MAIN

resultsET was established by observing decreased TNFα and increased IL-10 transcriptomic responses to two subsequent endotoxin challenges. Interestingly, ET was associated with increased S100A8 and S100A9 mRNA expression ex vivo. We showed that IL-10 played a role in this process, since S100A8 and S100A9 mRNA increases were significantly abrogated by IL-10 blockade in the model. Conversely, treatment with rIFN-γ, a pro-inflammatory and immunostimulating molecule known to block ET induction, was able to restore normal S100A8 and S100A9 mRNA in this model.

conclusionsIn this ex vivo model, we observed that S100A8 and S100A9 mRNA expression was significantly increased during ET. This reproduced ex vivo the observations we had previously made in septic shock patients. Interestingly, IL-10 blockade and rIFN-γ treatment partially abrogated S100A8/A9 mRNA increases in this model. Pending confirmation in larger, independent clinical studies, these preliminary results suggest that S100A8 and S100A9 mRNA levels might be used as surrogate markers of ET and as stratification tools for personalized immunotherapy in septic shock patients.

Indexed as

Models, BiologicalAdultCalgranulin ACalgranulin BFemaleGene Expression RegulationHumansImmune ToleranceInterferon-gammaInterleukin-10LipopolysaccharidesMaleMiddle AgedRNA, MessengerSuppressor of Cytokine Signaling 3 ProteinSuppressor of Cytokine Signaling ProteinsCalgranulin ACalgranulin BInterferon-gammaInterleukin-10LipopolysaccharidesRNA, MessengerSOCS3 protein, humanSuppressor of Cytokine Signaling 3 ProteinSuppressor of Cytokine Signaling ProteinsTumor Necrosis Factor-alpha

Identifiers

PMID24956170
PMCPMC4067416
OpenAlexW2011623901

What OpenQuestion holds

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LicenceCC BY
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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.