Evidence map›Paper›PMID 31258531›Full record

ReviewFrontiers in immunology2019

Fibrinolysis and Inflammation in Venous Thrombus Resolution.

Subhradip Mukhopadhyay, Tierra A Johnson, Nadire Duru, Marguerite S Buzza, Nisha R Pawar, Rajabrata Sarkar, Toni M Antalis

Open access · goldAbstract readReview
In one paragraph

Review 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 79 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
79citing papers in PubMed, 2 pooled it
11.5field-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

79 citing papers in PubMed, 2 syntheses or guidelines pooled it, 150 citations in OpenAlex.

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  15. Engineering the Immune Response to Biomaterials.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2025
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19 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

7 authors at 2 institutions in 1 country.

Subhradip MukhopadhyayCenter for Vascular and Inflammatory Diseases, University of Maryland School of Medicine, Baltimore, MD, United States.
Tierra A JohnsonCenter for Vascular and Inflammatory Diseases, University of Maryland School of Medicine, Baltimore, MD, United States.
Nadire DuruCenter for Vascular and Inflammatory Diseases, University of Maryland School of Medicine, Baltimore, MD, United States.
Marguerite S BuzzaCenter for Vascular and Inflammatory Diseases, University of Maryland School of Medicine, Baltimore, MD, United States.
Nisha R PawarCenter for Vascular and Inflammatory Diseases, University of Maryland School of Medicine, Baltimore, MD, United States.
Rajabrata SarkarCenter for Vascular and Inflammatory Diseases, University of Maryland School of Medicine, Baltimore, MD, United States.
Toni M AntalisCenter for Vascular and Inflammatory Diseases, University of Maryland School of Medicine, Baltimore, MD, United States.
University of Maryland, Baltimore · USUniversity of Maryland Marlene and Stewart Greenebaum Comprehensive Cancer Center

Funding

EXPAND PARTICIPATION BY MINORITIES IN BIOMEDICAL SCIENCER25GM055036 · NIGMS · UNIVERSITY OF MARYLAND BALTIMORE COUNTY · PI SUMMERS, MICHAEL FINLEY · 1996 to 2021
$16.9M
Vascular Biology Training ProgramT32HL007698 · NHLBI · UNIVERSITY OF MARYLAND BALTIMORE · PI Rosemary A Kozar, Dudley K. Strickland · 1991 to 2026
$8.7M
Training Grant in Cancer BiologyT32CA154274 · NCI · UNIVERSITY OF MARYLAND BALTIMORE · PI Toni M Antalis, CURT I CIVIN · 2011 to 2026
$6.8M
Membrane Serine Protease Activities in Protease Activated Receptor SignalingR01HL118390 · NHLBI · UNIVERSITY OF MARYLAND BALTIMORE · PI ANTALIS, TONI M · 2014 to 2017
$1.5M
Proteolytic Pathways in Venous Thrombus ResolutionI01BX001921 · VA · BALTIMORE VA MEDICAL CENTER · PI ANTALIS, TONI M · 2013 to 2025
–
BLRD VA I01 BX001921NCI NIH HHS T32 CA154274NHLBI NIH HHS R01 HL118390NHLBI NIH HHS T32 HL007698NIGMS NIH HHS R25 GM055036
6 · The paper itself

Abstract

Clinical observations and accumulating laboratory evidence support a complex interplay between coagulation, inflammation, innate immunity and fibrinolysis in venous thromboembolism (VTE). VTE, which includes deep vein thrombosis (DVT) and pulmonary embolism (PE), and the subsequent complications of post-thrombotic syndrome (PTS), are significant causes of morbidity and mortality in patients. Clinical risk factors for VTE include cancer, major trauma, surgery, sepsis, inflammatory bowel disease, paralysis, prolonged periods of immobility, and aging. Abnormalities in venous blood flow or stasis initiates the activation of endothelial cells, and in concert with platelets, neutrophils and monocytes, propagates VTE in an intact vein. In addition, inflammatory cells play crucial roles in thrombus recanalization and restoration of blood flow via fibrinolysis and vascular remodeling. Faster resolution of the thrombus is key for improved disease prognosis. While in the clinical setting, anticoagulation therapy is successful in preventing propagation of venous thrombi, current therapies are not designed to inhibit inflammation, which can lead to the development of PTS. Animal models of DVT have provided many insights into the molecular and cellular mechanisms involved in the formation, propagation, and resolution of venous thrombi as well as the roles of key components of the fibrinolytic system in these processes. Here, we review the recent advances in our understanding of fibrinolysis and inflammation in the resolution of VTE.

Indexed as

AnimalsBlood CoagulationDisease Models, AnimalEndothelial CellsFibrinolysisHumansImmunity, InnateInflammationVenous ThrombosisDVTfibrinolysisinflammationinnate immunityPEplasminogenvenous thromboembolismvenous thrombus resolution

Identifiers

PMID31258531
PMCPMC6587539
OpenAlexW2949751711

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.