Evidence map›Paper›PMID 37014925›Full record

ArticleClinical science (London, England : 1979)2023

Repetitive schistosoma exposure causes perivascular lung fibrosis and persistent pulmonary hypertension.

Rahul Kumar, Michael H Lee, Biruk Kassa, Dara C Fonseca Balladares, Claudia Mickael, Linda Sanders, Adam Andruska, Maya Kumar, Edda Spiekerkoetter, Angela Bandeira and 3 more

Open access · hybridAbstract read
In one paragraph

Article in Clinical science (London, England : 1979), 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
2.5field-weighted citation impact, top 13% 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

6 citing papers in PubMed, 9 citations in OpenAlex.

  1. IL-6 and TGF-β1 as biomarkers of schistosomiasis-associated pulmonary hypertension in a murine model.Brazilian journal of medical and biological research = Revista brasileira de pesquisas medicas e biologicas · 2026
    Article
  2. Article
  3. Review
  4. Intrapulmonary T Cells Are Sufficient forInternational journal of molecular sciences · 2024
    Article
  5. Interstitial macrophage phenotypes inFrontiers in immunology · 2024
    Article
  6. 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

13 authors at 4 institutions in 2 countries.

Rahul KumarDepartment of Medicine, Division of Pulmonary and Critical Care Medicine, University of California San Francisco, San Francisco, California, U.S.A.
Michael H LeeDepartment of Medicine, Division of Pulmonary and Critical Care Medicine, University of California San Francisco, San Francisco, California, U.S.A.
Biruk KassaDepartment of Medicine, Division of Pulmonary and Critical Care Medicine, University of California San Francisco, San Francisco, California, U.S.A.
Dara C Fonseca BalladaresDepartment of Medicine, Division of Pulmonary and Critical Care Medicine, University of California San Francisco, San Francisco, California, U.S.A.
Claudia MickaelDepartment of Medicine, Division of Pulmonary Sciences and Critical Care Medicine, University of Colorado Anschutz Medical Campus, Aurora, CO, U.S.A.
Linda SandersDepartment of Medicine, Division of Pulmonary Sciences and Critical Care Medicine, University of Colorado Anschutz Medical Campus, Aurora, CO, U.S.A.
Adam AndruskaDepartment of Medicine, Division of Pulmonary, Allergy and Critical Care Medicine, Stanford University, Palo Alto, CA, U.S.A.
Maya KumarDepartment of Pediatrics, Division of Pulmonary Medicine, Stanford University, Palo Alto, CA, U.S.A.
Edda SpiekerkoetterDepartment of Medicine, Division of Pulmonary, Allergy and Critical Care Medicine, Stanford University, Palo Alto, CA, U.S.A.
Angela BandeiraPROCAPE, Universidade de Pernambuco, Recife, Pernambuco, Brazil.
Kurt R StenmarkDepartment of Pediatrics, University of Colorado Anschutz Medical Campus, Aurora, CO, U.S.A.
Rubin M TuderDepartment of Medicine, Division of Pulmonary Sciences and Critical Care Medicine, University of Colorado Anschutz Medical Campus, Aurora, CO, U.S.A.
Brian B GrahamDepartment of Medicine, Division of Pulmonary and Critical Care Medicine, University of California San Francisco, San Francisco, California, U.S.A.ORCID 0000-0001-7541-2585
San Francisco General Hospital · USUniversity of Colorado Anschutz Medical Campus · USPalo Alto University · USUniversidade de Pernambuco · BR

Funding

Role of Complement-Driven Pulmonary Vascular Inflammation in PHP01HL152961 · NHLBI · UNIVERSITY OF COLORADO DENVER · PI STENMARK, KURT R. · 2020 to 2024
$14.1M
Investigating paclitaxel treatment in a pre-clinical model of Schistosoma-pulmonary hypertensionR01HL135872 · NHLBI · UNIVERSITY OF COLORADO DENVER · PI Brian Barkley Graham · 2017 to 2026
$5.1M
Defining the cellular and molecular mechanisms driving neointimal lesion growth in pulmonary hypertensionR01HL163013 · NHLBI · STANFORD UNIVERSITY · PI KUMAR, MAYA ELISE · 2022 to 2025
$2.7M
Targeting Novel BMPR2 modifiers in Pulmonary Hypertension with Repurposed DrugsR01HL128734 · NHLBI · STANFORD UNIVERSITY · PI SPIEKERKOETTER, EDDA FRAUKE · 2016 to 2020
$2.1M
Understanding and targeting molecular as well as structural events governing right ventricular adaptation, failure and recovery in pulmonary hypertension using repurposed drugsR01HL158868 · NHLBI · STANFORD UNIVERSITY · PI SPIEKERKOETTER, EDDA FRAUKE · 2021 to 2024
$1.7M
The contribution of hypoxia inducible factor-1-dependent glycolysis in lung interstitial macrophages to the pathobiology of schistosomiasis-induced pulmonary hypertension.K08HL168310 · NHLBI · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI Michael Hyunjean Lee · 2023 to 2026
$676k
NHLBI NIH HHS K08 HL168310NHLBI NIH HHS P01 HL152961NHLBI NIH HHS R01 HL128734NHLBI NIH HHS R01 HL135872NHLBI NIH HHS R01 HL158868NHLBI NIH HHS R01 HL163013NIAID NIH HHS HHSN272201300014I
6 · The paper itself

Abstract

backgroundPulmonary hypertension (PH) can occur as a complication of schistosomiasis. In humans, schistosomiasis-PH persists despite antihelminthic therapy and parasite eradication. We hypothesized that persistent disease arises as a consequence of exposure repetition.

methodsFollowing intraperitoneal sensitization, mice were experimentally exposed to Schistosoma eggs by intravenous injection, either once or three times repeatedly. The phenotype was characterized by right heart catheterization and tissue analysis.

resultsFollowing intraperitoneal sensitization, a single intravenous Schistosoma egg exposure resulted in a PH phenotype that peaked at 7-14 days, followed by spontaneous resolution. Three sequential exposures resulted in a persistent PH phenotype. Inflammatory cytokines were not significantly different between mice exposed to one or three egg doses, but there was an increase in perivascular fibrosis in those who received three egg doses. Significant perivascular fibrosis was also observed in autopsy specimens from patients who died of this condition.

conclusionsRepeatedly exposing mice to schistosomiasis causes a persistent PH phenotype, accompanied by perivascular fibrosis. Perivascular fibrosis may contribute to the persistent schistosomiasis-PH observed in humans with this disease.

Indexed as

Hypertension, PulmonaryPulmonary FibrosisSchistosomiasisAnimalsFibrosisHumansLungMiceSchistosoma mansoniFibrosisInflammationPulmonary hypertensionSchistosomiasisVascular remodeling

Identifiers

PMID37014925
PMCPMC10133871
OpenAlexW4362549487

What OpenQuestion holds

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LicenceCC BY-NC-ND
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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.