Evidence map›Paper›PMID 39337405›Full record

ArticleInternational journal of molecular sciences2024

Parvovirus B19 Infection Is Associated with the Formation of Neutrophil Extracellular Traps and Thrombosis: A Possible Linkage of the VP1 Unique Region.

Bor-Show Tzang, Hao-Yang Chin, Chih-Chen Tzang, Pei-Hua Chuang, Der-Yuan Chen, Tsai-Ching Hsu

Abstract read
In one paragraph

Article in International journal of molecular sciences, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

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

  1. Pooled it
  2. Neutrophil Extracellular Traps in Viral Infections.Pathogens (Basel, Switzerland) · 2025
    Pooled it
  3. Article
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

6 authors.

Bor-Show TzangInstitute of Medicine, Chung Shan Medical University, Taichung 402, Taiwan.ORCID 0000-0003-0140-9943
Hao-Yang ChinInstitute of Medicine, Chung Shan Medical University, Taichung 402, Taiwan.
Chih-Chen TzangSchool of Medicine, College of Medicine, National Taiwan University, Taipei City 100, Taiwan.
Pei-Hua ChuangInstitute of Medicine, Chung Shan Medical University, Taichung 402, Taiwan.
Der-Yuan ChenInstitute of Medicine, Chung Shan Medical University, Taichung 402, Taiwan.ORCID 0000-0003-1266-1423
Tsai-Ching HsuInstitute of Medicine, Chung Shan Medical University, Taichung 402, Taiwan.

Funding

National Science and Technology Council MOST 109-2314-B040-021 and NSTC 112-2314-B040-015
6 · The paper itself

Abstract

Neutrophil extracellular traps (NETs) formation, namely NETosis, is implicated in antiphospholipid syndrome (APS)-related thrombosis in various autoimmune disorders such as systemic lupus erythematosus (SLE) and APS. Human parvovirus B19 (B19V) infection is closely associated with SLE and APS and causes various clinical manifestations such as blood disorders, joint pain, fever, pregnancy complications, and thrombosis. Additionally, B19V may trigger the production of autoantibodies, including those against nuclear and phospholipid components. Thus, exploring the connection between B19V, NETosis, and thrombosis is highly relevant. An in vitro NETosis model using differentiated HL-60 neutrophil-like cells (dHL-60) was employed to investigate the effect of B19V-VP1u IgG on NETs formation. A venous stenosis mouse model was used to test how B19V-VP1u IgG-mediated NETs affect thrombosis in vivo. The NETosis was observed in the dHL-60 cells treated with rabbit anti-B19V-VP1u IgG and was inhibited in the presence of either 8-Br-cAMP or CGS216800 but not GSK484. Significantly elevated reactive oxygen species (ROS), myeloperoxidase (MPO), and citrullinated histone (Cit-H3) levels were detected in the dHL60 treated with phorbol myristate acetate (PMA), human aPLs IgG and rabbit anti-B19V-VP1u IgG, respectively. Accordingly, a significantly larger thrombus was observed in a venous stenosis-induced thrombosis mouse model treated with PMA, human aPLs IgG, rabbit anti-B19V-VP1u IgG, and human anti-B19V-VP1u IgG, respectively, along with significantly increased amounts of Cit-H3-, MPO- and CRAMP-positive infiltrated neutrophils in the thrombin sections. This research highlights that anti-B19V-VP1u antibodies may enhance the formation of NETosis and thrombosis and implies that managing and treating B19V infection could lower the risk of thrombosis.

Indexed as

Extracellular TrapsNeutrophilsParvovirus B19, HumanThrombosisAnimalsCapsid ProteinsDisease Models, AnimalHL-60 CellsHumansImmunoglobulin GMaleMiceParvoviridae InfectionsReactive Oxygen SpeciesCapsid Proteinscapsid protein VP1, parvovirus B19Immunoglobulin GReactive Oxygen Speciesantiphospholipid antibodies (aPLs)human parvovirus B19 (B19V)neutrophil extracellular traps (NETs)thrombosisVP1 unique region (VP1u) IgG

Identifiers

PMID39337405
PMCPMC11432092

What Socratic holds

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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.