Evidence map›Paper›PMID 31474979›Full record

ArticleFrontiers in immunology2019

Platelets Aggregate With Neutrophils and Promote Skin Pathology in Psoriasis.

Franziska Herster, Zsofia Bittner, Marius Cosmin Codrea, Nathan K Archer, Martin Heister, Markus W Löffler, Simon Heumos, Joanna Wegner, Ramona Businger, Michael Schindler and 6 more

Abstract read
In one paragraph

Article in Frontiers in immunology, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 28 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
28citing papers in PubMed, 2 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

28 citing papers in PubMed, 2 syntheses or guidelines pooled it.

  1. Pooled it
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  12. Observational
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  19. Article
  20. Neutrophils in chronic inflammatory diseases.Cellular & molecular immunology · 2022
    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

16 authors.

Franziska HersterDepartment of Immunology, University of Tübingen, Tübingen, Germany.
Zsofia BittnerDepartment of Immunology, University of Tübingen, Tübingen, Germany.
Marius Cosmin CodreaQuantitative Biology Center, University of Tübingen, Tübingen, Germany.
Nathan K ArcherDepartment of Dermatology, Johns Hopkins University School of Medicine, Baltimore, MD, United States.
Martin HeisterDepartment of Dermatology, University Hospital Tübingen, Tübingen, Germany.
Markus W LöfflerDepartment of Immunology, University of Tübingen, Tübingen, Germany.
Simon HeumosQuantitative Biology Center, University of Tübingen, Tübingen, Germany.
Joanna WegnerDepartment of Dermatology, University Hospital Mainz, Mainz, Germany.
Ramona BusingerDivision of Molecular Virology, Institute of Virology, Tübingen, Germany.
Michael SchindlerDivision of Molecular Virology, Institute of Virology, Tübingen, Germany.
David StegnerInstitute of Experimental Biomedicine, University Hospital and Rudolf Virchow Center, University of Würzburg, Würzburg, Germany.
Knut SchäkelDepartment of Dermatology, University Hospital Heidelberg, Heidelberg, Germany.
Stephan GrabbeDepartment of Dermatology, University Hospital Mainz, Mainz, Germany.
Kamran GhoreschiDepartment of Dermatology, University Hospital Tübingen, Tübingen, Germany.
Lloyd S MillerDepartment of Dermatology, Johns Hopkins University School of Medicine, Baltimore, MD, United States.
Alexander N R WeberDepartment of Immunology, University of Tübingen, Tübingen, Germany.

Funding

IL-36 responses in Staphylococcus aureus driven skin inflammationR01AR073665 · NIAMS · JOHNS HOPKINS UNIVERSITY · PI ARCHER, NATHAN K. · 2018 to 2022
$1.8M
STAT3-mediated immunity to Staphylococcus aureus in skinR01AR069502 · NIAMS · JOHNS HOPKINS UNIVERSITY · PI ARCHER, NATHAN K. · 2016 to 2020
$1.8M
NIAMS NIH HHS R01 AR069502NIAMS NIH HHS R01 AR073665
6 · The paper itself

Abstract

Psoriasis is a frequent systemic inflammatory autoimmune disease characterized primarily by skin lesions with massive infiltration of leukocytes, but frequently also presents with cardiovascular comorbidities. Especially polymorphonuclear neutrophils (PMNs) abundantly infiltrate psoriatic skin but the cues that prompt PMNs to home to the skin are not well-defined. To identify PMN surface receptors that may explain PMN skin homing in psoriasis patients, we screened 332 surface antigens on primary human blood PMNs from healthy donors and psoriasis patients. We identified platelet surface antigens as a defining feature of psoriasis PMNs, due to a significantly increased aggregation of neutrophils and platelets in the blood of psoriasis patients. Similarly, in the imiquimod-induced experimental

Indexed as

AdultAnimalsBlood PlateletsHumansImiquimodMiceMice, Inbred C57BLNeutrophilsPlatelet ActivationPlatelet AggregationPlatelet CountPsoriasisSkinImiquimodimiquimodneutrophilplateletplatelet-neutrophil complexes (PNCs)psoriasis

Identifiers

PMID31474979
PMCPMC6706802

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Registered trials

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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.