Evidence map›Paper›PMID 38034031›Full record

ArticleMolecular therapy. Nucleic acids2023

Cationic LNP-formulated mRNA expressing Tie2-agonist in the lung endothelium prevents pulmonary vascular leakage.

Katrin Radloff, Birgitt Gutbier, Charlotte Maeve Dunne, Hanieh Moradian, Marko Schwestka, Manfred Gossen, Katharina Ahrens, Laura Kneller, Yadong Wang, Akanksha Moga and 8 more

Open access · goldAbstract read
In one paragraph

Article in Molecular therapy. Nucleic acids, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
2.6field-weighted citation impact, top 8% 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

10 citing papers in PubMed, 12 citations in OpenAlex.

  1. Review
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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

18 authors at 3 institutions in 1 country.

Katrin RadloffPantherna Therapeutics GmbH, 16761 Hennigsdorf, Germany.
Birgitt GutbierCharité - Universitätsmedizin Berlin, Corporate Member of Freie Universität Berlin and Humboldt-Universität zu Berlin, Department of Infectious Diseases, Respiratory Medicine, and Critical Care, 10117 Berlin, Germany.
Charlotte Maeve DunnePantherna Therapeutics GmbH, 16761 Hennigsdorf, Germany.
Hanieh MoradianInstitute of Active Polymers, Helmholtz-Zentrum Hereon, 14513 Teltow, Germany.
Marko SchwestkaInstitute of Active Polymers, Helmholtz-Zentrum Hereon, 14513 Teltow, Germany.
Manfred GossenInstitute of Active Polymers, Helmholtz-Zentrum Hereon, 14513 Teltow, Germany.
Katharina AhrensCharité - Universitätsmedizin Berlin, Corporate Member of Freie Universität Berlin and Humboldt-Universität zu Berlin, Department of Infectious Diseases, Respiratory Medicine, and Critical Care, 10117 Berlin, Germany.
Laura KnellerCharité - Universitätsmedizin Berlin, Corporate Member of Freie Universität Berlin and Humboldt-Universität zu Berlin, Department of Infectious Diseases, Respiratory Medicine, and Critical Care, 10117 Berlin, Germany.
Yadong WangCharité - Universitätsmedizin Berlin, Corporate Member of Freie Universität Berlin and Humboldt-Universität zu Berlin, Department of Infectious Diseases, Respiratory Medicine, and Critical Care, 10117 Berlin, Germany.
Akanksha MogaPantherna Therapeutics GmbH, 16761 Hennigsdorf, Germany.
Leonidas GkionisPantherna Therapeutics GmbH, 16761 Hennigsdorf, Germany.
Oliver KeilPantherna Therapeutics GmbH, 16761 Hennigsdorf, Germany.
Volker FehringPantherna Therapeutics GmbH, 16761 Hennigsdorf, Germany.
Daniel TonderaPantherna Therapeutics GmbH, 16761 Hennigsdorf, Germany.
Klaus GiesePantherna Therapeutics GmbH, 16761 Hennigsdorf, Germany.
Ansgar SantelPantherna Therapeutics GmbH, 16761 Hennigsdorf, Germany.
Jörg KaufmannPantherna Therapeutics GmbH, 16761 Hennigsdorf, Germany.
Martin WitzenrathCharité - Universitätsmedizin Berlin, Corporate Member of Freie Universität Berlin and Humboldt-Universität zu Berlin, Department of Infectious Diseases, Respiratory Medicine, and Critical Care, 10117 Berlin, Germany.
Cleopa (Germany) · DEHelmholtz-Zentrum Hereon · DECharité - Universitätsmedizin Berlin · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Dysfunction of endothelial cells (ECs) lining the inner surface of blood vessels are causative for a number of diseases. Hence, the ability to therapeutically modulate gene expression within ECs is of high therapeutic value in treating diseases such as those associated with lung edema. mRNAs formulated with lipid nanoparticles (LNPs) have emerged as a new drug modality to induce transient protein expression for modulating disease-relevant signal transduction pathways. In the study presented here, we tested the effect of a novel synthetic, nucleoside-modified mRNA encoding COMP-Ang1 (mRNA-76) formulated into a cationic LNP on attenuating inflammation-induced vascular leakage. After intravenous injection, the respective mRNA was found to be delivered almost exclusively to the ECs of the lung, while sparing other vascular beds and bypassing the liver. The mode of action of mRNA-76, such as its activation of the Tie2 signal transduction pathway, was tested by pharmacological studies

Indexed as

acute respiratory distress syndromeARDScationic lipid nanoparticlesedemaendotheliummRNAMT: Oligonucleotides: Therapies and Applicationstherapeutic modulation of gene expressiontissue-specific targeting of the lung vasculature

Identifiers

PMID38034031
PMCPMC10682670
OpenAlexW4388011913

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.