Evidence map›Paper›PMID 37467233›Full record

ArticlePLoS pathogens2023

S100A9 is indispensable for survival of pneumococcal pneumonia in mice.

Lena Ostermann, Benjamin Seeliger, Sascha David, Carolin Flasche, Regina Maus, Marieke S Reinboth, Martin Christmann, Konstantin Neumann, Korbinian Brand, Stephan Seltmann and 7 more

Open access · goldAbstract read
In one paragraph

Article in PLoS pathogens, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed, 1 pooled it
1.2field-weighted citation impact, top 21% 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

8 citing papers in PubMed, 1 synthesis or guideline pooled it, 8 citations in OpenAlex.

  1. Pooled it
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  7. Article
  8. The oxidative stress response ofFrontiers in microbiology · 2023
    Review
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

17 authors at 5 institutions in 3 countries.

Lena OstermannDivision of Experimental Pneumology, Hannover Medical School, Hannover, Germany.
Benjamin SeeligerClinic for Pneumology, Hannover Medical School, Hannover, Germany.
Sascha DavidInstitute of Intensive Care Medicine, University Hospital Zurich, Zurich, Switzerland.
Carolin FlascheDivision of Experimental Pneumology, Hannover Medical School, Hannover, Germany.
Regina MausDivision of Experimental Pneumology, Hannover Medical School, Hannover, Germany.
Marieke S ReinbothDivision of Experimental Pneumology, Hannover Medical School, Hannover, Germany.
Martin ChristmannInstitute of Clinical Chemistry, Hannover Medical School, Hannover, Germany.
Konstantin NeumannInstitute of Clinical Chemistry, Hannover Medical School, Hannover, Germany.
Korbinian BrandInstitute of Clinical Chemistry, Hannover Medical School, Hannover, Germany.
Stephan SeltmannLabopart Medical Laboratories, Dresden and Chemnitz, Germany.
Frank BühlingLabopart Medical Laboratories, Dresden and Chemnitz, Germany.
James C PatonResearch Centre for Infectious Diseases, Department of Molecular and Biomedical Science, University of Adelaide, Adelaide, Australia.
Johannes RothInstitute of Immunology, University of Münster, Münster, Germany.
Thomas VoglInstitute of Immunology, University of Münster, Münster, Germany.
Dorothee ViemannDepartment of Pediatric Pneumology, Allergology and Neonatology, Hannover Medical School, Hannover, Germany.
Tobias WelteClinic for Pneumology, Hannover Medical School, Hannover, Germany.
Ulrich A MausDivision of Experimental Pneumology, Hannover Medical School, Hannover, Germany.ORCID 0000-0002-6172-8746
Medizinische Hochschule Hannover · DEKlinikum Chemnitz · DEUniversity of Münster · DEThe University of Adelaide · AUUniversity Hospital of Zurich · CH

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

S100A8/A9 has important immunomodulatory roles in antibacterial defense, but its relevance in focal pneumonia caused by Streptococcus pneumoniae (S. pneumoniae) is understudied. We show that S100A9 was significantly increased in BAL fluids of patients with bacterial but not viral pneumonia and correlated with procalcitonin and sequential organ failure assessment scores. Mice deficient in S100A9 exhibited drastically elevated Zn2+ levels in lungs, which led to bacterial outgrowth and significantly reduced survival. In addition, reduced survival of S100A9 KO mice was characterized by excessive release of neutrophil elastase, which resulted in degradation of opsonophagocytically important collectins surfactant proteins A and D. All of these features were attenuated in S. pneumoniae-challenged chimeric WT→S100A9 KO mice. Similarly, therapy of S. pneumoniae-infected S100A9 KO mice with a mutant S100A8/A9 protein showing increased half-life significantly decreased lung bacterial loads and lung injury. Collectively, S100A9 controls central antibacterial immune mechanisms of the lung with essential relevance to survival of pneumococcal pneumonia. Moreover, S100A9 appears to be a promising biomarker to distinguish patients with bacterial from those with viral pneumonia. Trial registration: Clinical Trials register (DRKS00000620).

Indexed as

Pneumonia, PneumococcalAnimalsBacteriaCalgranulin ACalgranulin BLungMiceMice, KnockoutStreptococcus pneumoniaeCalgranulin ACalgranulin BS100A9 protein, mouse

Identifiers

PMID37467233
PMCPMC10355425
OpenAlexW4384820179

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.