Evidence map›Paper›PMID 37451977›Full record

ReviewHematology, transfusion and cell therapy

Immunothrombosis and its underlying biological mechanisms.

Arthur Cunha De Nardi, Andréa Coy-Canguçu, Atena Saito, Maria Fernanda Florio, Giovanna Marti, Giovanna R Degasperi, Fernanda A Orsi

Open access · diamondAbstract readReview
In one paragraph

Review in Hematology, transfusion and cell therapy. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 28 papers.

0numbers the graph read from it
0cells of the map it votes in
28citing papers in PubMed
3.5field-weighted citation impact, top 7% 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

28 citing papers in PubMed, 22 citations in OpenAlex.

  1. Review
  2. Article
  3. Incident atrial fibrillation and pyoderma gangrenosum: long-term thromboembolic, heart failure, and mortality risk.Clinical research in cardiology : official journal of the German Cardiac Society · 2026
    Article
  4. Review
  5. Article
  6. Hemostasis at the edge between physiology and cancer.Internal and emergency medicine · 2026
    Review
  7. Article
  8. Review
  9. Review
  10. Article
  11. Article
  12. Review
  13. Review
  14. Article
  15. Review
  16. Article
  17. Article
  18. Review
  19. Article
  20. 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

7 authors at 2 institutions in 1 country.

Arthur Cunha De NardiPontifícia Universidade Católica de Campinas (PUCC), Faculdade de Medicina, Campinas, Brazil.
Andréa Coy-CanguçuPontifícia Universidade Católica de Campinas (PUCC), Faculdade de Medicina, Campinas, Brazil. Electronic address: andreacangucupuc@gmail.com.
Atena SaitoPontifícia Universidade Católica de Campinas (PUCC), Faculdade de Medicina, Campinas, Brazil.
Maria Fernanda FlorioPontifícia Universidade Católica de Campinas (PUCC), Faculdade de Medicina, Campinas, Brazil.
Giovanna MartiPontifícia Universidade Católica de Campinas (PUCC), Faculdade de Medicina, Campinas, Brazil.
Giovanna R DegasperiPontifícia Universidade Católica de Campinas (PUCC), Faculdade de Medicina, Campinas, Brazil.
Fernanda A OrsiUniversidade Estadual de Campinas (UNICAMP), Faculdade de Ciências Médicas, Departamento de Patologia, Campinas, Brazil.
Pontifícia Universidade Católica de Campinas · BRUniversidade Estadual de Campinas (UNICAMP) · BR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The evolutionary conserved link between coagulation and innate immunity is a biological process characterized by the thrombosis formation stimulus of immune cells and specific thrombosis-related molecules. In physiological settings, the relationship between the immune system and thrombosis facilitates the recognition of pathogens and damaged cells and inhibits pathogen proliferation. However, when deregulated, the interplay between hemostasis and innate immunity becomes a pathological process named immunothrombosis, which is at the basis of several infectious and inflammation-related thrombotic disorders, including coronavirus disease 2019 (COVID-19). In advanced stages, alterations in both coagulation and immune cell function due to extreme inflammation lead to an increase in blood coagulability, with high rates of thrombosis and mortality. Therefore, understanding underlying mechanisms in immunothrombosis has become decisive for the development of more efficient therapies to treat and prevent thrombosis in COVID-19 and in other thrombotic disorders. In this review, we outline the existing knowledge on the molecular and cellular processes involved in immunothrombosis, focusing on the role of neutrophil extracellular traps (NETs), platelets and the coagulation pathway. We also describe how the deregulation of hemostasis is associated with pathological conditions and can significantly aggravate a patient's condition, using COVID-19 as a clinical model.

Indexed as

Blood coagulationCOVID-19Immune systemImmunothrombosisThromboinflammation

Identifiers

PMID37451977
PMCPMC10935458
OpenAlexW4382810129

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.