Evidence map›Paper›PMID 30852423›Full record

ArticleBiomaterials2019

Hydrogel-based delivery of Il-10 improves treatment of bleomycin-induced lung fibrosis in mice.

Elya A Shamskhou, Michael J Kratochvil, Mark E Orcholski, Nadine Nagy, Gernot Kaber, Emily Steen, Swathi Balaji, Ke Yuan, Sundeep Keswani, Ben Danielson and 6 more

Open access · greenAbstract read
In one paragraph

Article in Biomaterials, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 50 papers.

0numbers the graph read from it
0cells of the map it votes in
50citing papers in PubMed
8.4field-weighted citation impact, top 2% 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

50 citing papers in PubMed, 107 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Review
  5. Article
  6. Article
  7. Article
  8. Review
  9. Article
  10. Review
  11. Hydrogel applications: a promising frontier in pneumonia therapy.Frontiers in bioengineering and biotechnology · 2025
    Review
  12. IL-10 mediates pleural remodeling in systemic lupus erythematosus.Cell communication and signaling : CCS · 2024
    Article
  13. Article
  14. Article
  15. Article
  16. The complex role of IL-10 in malignant ascites: a review.Cancer immunology, immunotherapy : CII · 2024
    Review
  17. Stimulus-Responsive Hydrogels as Drug Delivery Systems for Inflammation Targeted Therapy.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2024
    Review
  18. Article
  19. Review
  20. Inflammation and aging: signaling pathways and intervention therapies.Signal transduction and targeted therapy · 2023
    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

16 authors at 2 institutions in 1 country.

Elya A ShamskhouDepartment of Medicine, Division of Pulmonary and Critical Care Medicine, Stanford University, Stanford, CA, 94305, USA.
Michael J KratochvilDepartment of Materials Science and Engineering, Stanford University, Stanford, CA, 94305, USA; Department of Medicine, Division of Infectious Disease, Stanford University, Stanford, CA, 94305, USA.
Mark E OrcholskiDepartment of Medicine, Division of Pulmonary and Critical Care Medicine, Stanford University, Stanford, CA, 94305, USA.
Nadine NagyDepartment of Medicine, Division of Infectious Disease, Stanford University, Stanford, CA, 94305, USA.
Gernot KaberDepartment of Medicine, Division of Infectious Disease, Stanford University, Stanford, CA, 94305, USA.
Emily SteenDepartment of Surgery, Division of Pediatric Surgery, Baylor College of Medicine and Texas Children's Hospital, Houston, TX, 77030, USA.
Swathi BalajiDepartment of Surgery, Division of Pediatric Surgery, Baylor College of Medicine and Texas Children's Hospital, Houston, TX, 77030, USA.
Ke YuanDepartment of Medicine, Division of Pulmonary and Critical Care Medicine, Stanford University, Stanford, CA, 94305, USA.
Sundeep KeswaniDepartment of Surgery, Division of Pediatric Surgery, Baylor College of Medicine and Texas Children's Hospital, Houston, TX, 77030, USA.
Ben DanielsonDepartment of Medicine, Division of Infectious Disease, Stanford University, Stanford, CA, 94305, USA.
Max GaoDepartment of Medicine, Division of Pulmonary and Critical Care Medicine, Stanford University, Stanford, CA, 94305, USA.
Carlos MedinaDepartment of Medicine, Division of Infectious Disease, Stanford University, Stanford, CA, 94305, USA.
Abinaya NathanDepartment of Medicine, Division of Pulmonary and Critical Care Medicine, Stanford University, Stanford, CA, 94305, USA.
Ananya ChakrabortyDepartment of Medicine, Division of Pulmonary and Critical Care Medicine, Stanford University, Stanford, CA, 94305, USA.
Paul L BollykyDepartment of Medicine, Division of Infectious Disease, Stanford University, Stanford, CA, 94305, USA.
Vinicio A De Jesus PerezDepartment of Medicine, Division of Pulmonary and Critical Care Medicine, Stanford University, Stanford, CA, 94305, USA. Electronic address: vdejesus@stanford.edu.
Stanford University · USBaylor College of Medicine · US

Funding

MOLECULAR &CELLULAR IMMUNOBIOLOGYT32AI007290 · NIAID · STANFORD UNIVERSITY · PI Sean Curtis Bendall, Olivia M Martinez · 1985 to 2026
$27.0M
The Wnt7a/ROR2 axis in the pathogenesis of pulmonary arterial hypertensionR01HL134776 · NHLBI · STANFORD UNIVERSITY · PI DE JESUS PEREZ, VINICIO A · 2017 to 2025
$5.0M
Endothelial-pericyte interactions in the pathogenesis of pulmonary arterial hypertensionR01HL139664 · NHLBI · STANFORD UNIVERSITY · PI DE JESUS PEREZ, VINICIO A · 2018 to 2025
$4.7M
Novel Mechanisms of Regenerative Wound HealingR01GM111808 · NIGMS · CINCINNATI CHILDRENS HOSP MED CTR · PI Sundeep G Keswani · 2014 to 2026
$3.6M
The role of the Wnt5a/ROR2 in the pathogenesis of pulmonary arterial hypertension.R03HL133423 · NHLBI · STANFORD UNIVERSITY · PI DE JESUS PEREZ, VINICIO A · 2016 to 2017
$159k
NHLBI NIH HHS R01 HL134776NHLBI NIH HHS R01 HL139664NHLBI NIH HHS R03 HL133423NIAID NIH HHS T32 AI007290NIGMS NIH HHS R01 GM111808
6 · The paper itself

Abstract

Idiopathic pulmonary fibrosis (IPF) is a life-threatening progressive lung disorder with limited therapeutic options. While interleukin-10 (IL-10) is a potent anti-inflammatory and anti-fibrotic cytokine, its utility in treating lung fibrosis has been limited by its short half-life. We describe an innovative hydrogel-based approach to deliver recombinant IL-10 to the lung for the prevention and reversal of pulmonary fibrosis in a mouse model of bleomycin-induced lung injury. Our studies show that a hyaluronan and heparin-based hydrogel system locally delivers IL-10 by capitalizing on the ability of heparin to reversibly bind IL-10 without bleeding or other complications. This formulation is significantly more effective than soluble IL-10 for both preventing and reducing collagen deposition in the lung parenchyma after 7 days of intratracheal administration. The anti-fibrotic effect of IL-10 in this system is dependent on suppression of TGF-β driven collagen production by lung fibroblasts and myofibroblasts. We conclude that hydrogel-based delivery of IL-10 to the lung is a promising therapy for fibrotic lung disorders.

Indexed as

AnimalsBleomycinCells, CulturedEnzyme-Linked Immunosorbent AssayFluorescent Antibody TechniqueHumansHyaluronic AcidHydrogelsImmunohistochemistryInterleukin-10MicePulmonary FibrosisBleomycinHyaluronic AcidHydrogelsInterleukin-10Drug deliveryFibrosisHyaluronic acidHydrogelIdiopathic pulmonary fibrosisInterleukin-10

Identifiers

PMID30852423
PMCPMC6430662
OpenAlexW2915555769

What OpenQuestion holds

Textmetadata
LicenceTDM
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.