Evidence map›Paper›PMID 31989082›Full record

ReviewResearch and practice in thrombosis and haemostasis2020

The dual role of platelet-innate immune cell interactions in thrombo-inflammation.

Julie Rayes, Joshua H Bourne, Alexander Brill, Steve P Watson

Open access · goldAbstract readReview
In one paragraph

Review in Research and practice in thrombosis and haemostasis, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 98 papers.

0numbers the graph read from it
0cells of the map it votes in
98citing papers in PubMed
13.3field-weighted citation impact, top 1% 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

98 citing papers in PubMed, 182 citations in OpenAlex.

  1. Article
  2. Advances in nucleotide-based P2Y₁ antagonism: implications for cardiovascular therapeutics.Medicinal chemistry research : an international journal for rapid communications on design and mechanisms of action of biologically active agents · 2026
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  11. CD11cBiomedicines · 2026
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  17. Computational Modeling of Pro-inflammatory Cytokine-Enhanced Blood Coagulation.Computational and structural biotechnology journal · 2026
    Article
  18. Article
  19. Article
  20. Article

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

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

4 authors at 3 institutions in 2 countries.

Julie RayesInstitute of Cardiovascular Sciences College of Medical and Dental Sciences University of Birmingham Birmingham UK.ORCID https://orcid.org/0000-0003-0499-6880
Joshua H BourneInstitute of Cardiovascular Sciences College of Medical and Dental Sciences University of Birmingham Birmingham UK.ORCID https://orcid.org/0000-0003-4442-5767
Alexander BrillInstitute of Cardiovascular Sciences College of Medical and Dental Sciences University of Birmingham Birmingham UK.ORCID https://orcid.org/0000-0002-4558-0390
Steve P WatsonInstitute of Cardiovascular Sciences College of Medical and Dental Sciences University of Birmingham Birmingham UK.ORCID https://orcid.org/0000-0002-7846-7423
West Midlands Deanery · GBSechenov University · RUUniversity of Birmingham · GB

Funding

British Heart Foundation FS/19/30/34173British Heart Foundation RG/13/18/30563
6 · The paper itself

Abstract

Beyond their role in hemostasis and thrombosis, platelets are increasingly recognized as key regulators of the inflammatory response under sterile and infectious conditions. Both platelet receptors and secretion are critical for these functions and contribute to their interaction with the endothelium and innate immune system. Platelet-leukocyte interactions are increased in thrombo-inflammatory diseases and are sensitive biomarkers for platelet activation and targets for the development of new therapies. The crosstalk between platelets and innate immune cells promotes thrombosis, inflammation, and tissue damage. However, recent studies have shown that these interactions also regulate the resolution of inflammation, tissue repair, and wound healing. Many of the platelet and leukocyte receptors involved in these bidirectional interactions are not selective for a subset of immune cells. However, specific heterotypic interactions occur in different vascular beds and inflammatory conditions, raising the possibility of disease- and organ-specific pathways of intervention. In this review, we highlight and discuss prominent and emerging interrelationships between platelets and innate immune cells and their dual role in the regulation of the inflammatory response in sterile and infectious thrombo-inflammatory diseases. A better understanding of the functional relevance of these interactions in different vascular beds may provide opportunities for successful therapeutic interventions to regulate the development, progression, and chronicity of various pathological processes.

Indexed as

immune cellsinflammationplateletsthrombo‐inflammationthrombosis

Identifiers

PMID31989082
PMCPMC6971330
OpenAlexW2981036457

What Socratic 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 Socratic graph.