Evidence map›Paper›PMID 36642345›Full record

ArticleEuropean journal of pharmaceutical sciences : official journal of the European Federation for Pharmaceutical Sciences2023

Lipid nanoparticle-mediated mRNA delivery in lung fibrosis.

Matteo Massaro, Suhong Wu, Gherardo Baudo, Haoran Liu, Scott Collum, Hyunho Lee, Cinzia Stigliano, Victor Segura-Ibarra, Harry Karmouty-Quintana, Elvin Blanco

Open access · goldAbstract read
In one paragraph

Article in European journal of pharmaceutical sciences : official journal of the European Federation for Pharmaceutical Sciences, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 30 papers.

0numbers the graph read from it
0cells of the map it votes in
30citing papers in PubMed
14.5field-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

30 citing papers in PubMed, 56 citations in OpenAlex.

  1. Review
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  5. Article
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  7. Engineering function in lung biology: integrating imaging, regenerative constructs, and functional biodesign.American journal of physiology. Lung cellular and molecular physiology · 2026
    Review
  8. Review
  9. Review
  10. Review
  11. Article
  12. Article
  13. Developing Biomaterial-Based mRNA Delivery System for Lung Disease Treatment.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2025
    Review
  14. Review
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  16. Article
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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

10 authors at 2 institutions in 2 countries.

Matteo MassaroDepartment of Nanomedicine, Houston Methodist Research Institute, Houston, TX 77030 United States; College of Materials Sciences and Opto-Electronic Technology, University of Chinese Academy of Sciences, Beijing 100049 China.
Suhong WuDepartment of Nanomedicine, Houston Methodist Research Institute, Houston, TX 77030 United States.
Gherardo BaudoDepartment of Nanomedicine, Houston Methodist Research Institute, Houston, TX 77030 United States; College of Materials Sciences and Opto-Electronic Technology, University of Chinese Academy of Sciences, Beijing 100049 China.
Haoran LiuDepartment of Nanomedicine, Houston Methodist Research Institute, Houston, TX 77030 United States.
Scott CollumDepartment of Biochemistry and Molecular Biology, Divisions of Critical Care, Pulmonary and Sleep Medicine, Department of Internal Medicine, University of Texas Health Science Center at Houston, Houston, TX 77030, United States.
Hyunho LeeDepartment of Nanomedicine, Houston Methodist Research Institute, Houston, TX 77030 United States.
Cinzia StiglianoDepartment of Neurosurgery, Center for Neuroregeneration, Houston Methodist Research Institute, Houston, TX 77030 United States.
Victor Segura-IbarraDepartment of Nanomedicine, Houston Methodist Research Institute, Houston, TX 77030 United States.
Harry Karmouty-QuintanaDepartment of Biochemistry and Molecular Biology, Divisions of Critical Care, Pulmonary and Sleep Medicine, Department of Internal Medicine, University of Texas Health Science Center at Houston, Houston, TX 77030, United States.
Elvin BlancoDepartment of Nanomedicine, Houston Methodist Research Institute, Houston, TX 77030 United States; Department of Cardiology, Houston Methodist DeBakey Heart and Vascular Center, Houston Methodist Hospital, Houston, TX 77030 United States; Department of Medicine, Weill Cornell Medical College, New York, NY 10065, United States. Electronic address: eblanco@houstonmethodist.org.
Houston Methodist · USThe University of Texas Health Science Center at Houston · US

Funding

Sineoculis Homeobox Homolog 1 (Six1) in Pulmonary FibrosisR01HL157100 · NHLBI · UNIVERSITY OF TEXAS HLTH SCI CTR HOUSTON · PI KARMOUTY-QUINTANA, HARRY · 2021 to 2025
$2.8M
NHLBI NIH HHS R01 HL157100
6 · The paper itself

Abstract

mRNA delivery enables the specific synthesis of proteins with therapeutic potential, representing a powerful strategy in diseases lacking efficacious pharmacotherapies. Idiopathic pulmonary fibrosis (IPF) is a chronic lung disease characterized by excessive extracellular matrix (ECM) deposition and subsequent alveolar remodeling. Alveolar epithelial type 2 cells (AEC2) and fibroblasts represent important targets in IPF given their role in initiating and driving aberrant wound healing responses that lead to excessive ECM deposition. Our objective was to examine a lipid nanoparticle (LNP)-based mRNA construct as a viable strategy to target alveolar epithelial cells and fibroblasts in IPF. mRNA-containing LNPs measuring ∼34 nm had high encapsulation efficiency, protected mRNA from degradation, and exhibited sustained release kinetics. eGFP mRNA LNP transfection in human primary cells proved dose- and time-dependent in vitro. In a bleomycin mouse model of lung fibrosis, luciferase mRNA LNPs administered intratracheally led to site-specific lung accumulation. Importantly, bioluminescence signal was detected in lungs as early as 2 h after delivery, with signal still evident at 48 h. Of note, LNPs were found associated with AEC2 and fibroblasts in vivo. Findings highlight the potential for pulmonary delivery of mRNA in IPF, opening therapeutic avenues aimed at halting and potentially reversing disease progression.

Indexed as

Idiopathic Pulmonary FibrosisSignal TransductionAnimalsBleomycinFibroblastsHumansLiposomesLungMiceNanoparticlesRNA, MessengerBleomycinLipid NanoparticlesLiposomesRNA, MessengerAlveolar epithelial cellsGene deliveryIdiopathic pulmonary fibrosisLipid nanoparticles (LNPs)Lung fibroblastsmRNA

Identifiers

PMID36642345
PMCPMC10898324
OpenAlexW4316674627

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.