Evidence map›Paper›PMID 31882941›Full record

ArticleScientific reports2019

Effective lung-targeted RNAi in mice with peptide-based delivery of nucleic acid.

Kaido Kurrikoff, Krista Freimann, Kadi-Liis Veiman, Elin Madli Peets, Andres Piirsoo, Ülo Langel

Abstract read
In one paragraph

Article in Scientific reports, 2019. 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
–field-weighted citation impact
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.

  1. Article
  2. Review
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  6. Review
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  9. Article
  10. Lauroylated Histidine-Enriched S4Pharmaceutical research · 2020
    Article
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

6 authors.

Kaido KurrikoffInstitute of Technology, University of Tartu, Nooruse 1, 50411, Tartu, Estonia. kaido.kurrikoff@ut.ee.
Krista FreimannInstitute of Technology, University of Tartu, Nooruse 1, 50411, Tartu, Estonia.
Kadi-Liis VeimanInstitute of Technology, University of Tartu, Nooruse 1, 50411, Tartu, Estonia.
Elin Madli PeetsInstitute of Technology, University of Tartu, Nooruse 1, 50411, Tartu, Estonia.
Andres PiirsooInstitute of Technology, University of Tartu, Nooruse 1, 50411, Tartu, Estonia.
Ülo LangelInstitute of Technology, University of Tartu, Nooruse 1, 50411, Tartu, Estonia.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

We have previously developed efficient peptide-based nucleic acid delivery vectors PF14 and NF55, where we have shown that these vectors preferentially transfect lung tissue upon systemic administration with the nucleic acid. In the current work, we have explored the utilization and potential of these vectors for the lung-targeted gene therapy. Accordingly, we assessed the efficacy of these peptides in (i) two different lung disease models - acute lung inflammation and asthma in mice and (ii) using two different nucleic acid cargos - siRNA and pDNA encoding shRNA. Using RNAi against cytokine TNFα, we showed efficient anti-inflammatory effects in both disease models and observed decreased disease symptoms. Our results highlight the potential of our transfection vectors for lung gene therapy.

Indexed as

AnimalsAsthmaFemaleGenetic TherapyInflammationLungMaleMiceNucleic AcidsPolymerase Chain ReactionRNA InterferenceNucleic Acids

Identifiers

PMID31882941
PMCPMC6934651

What OpenQuestion holds

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LicenceCC BY
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Registered trials

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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.