Evidence map›Paper›PMID 33661555›Full record

ReviewAdvanced healthcare materials2021

Therapeutic RNA Delivery for COVID and Other Diseases.

Curtis Dobrowolski, Kalina Paunovska, Marine Z C Hatit, Melissa P Lokugamage, James E Dahlman

Open access · greenAbstract readReview
In one paragraph

Review in Advanced healthcare materials, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 27 papers.

0numbers the graph read from it
0cells of the map it votes in
27citing papers in PubMed
3.5field-weighted citation impact, top 6% 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

27 citing papers in PubMed, 62 citations in OpenAlex.

  1. Review
  2. Review
  3. Review
  4. Review
  5. Article
  6. Article
  7. Review
  8. A perspective of lipid nanoparticles for RNA delivery.Exploration (Beijing, China) · 2024
    Article
  9. Review
  10. Endosomal escape: A bottleneck for LNP-mediated therapeutics.Proceedings of the National Academy of Sciences of the United States of America · 2024
    Review
  11. tRNA therapeutics for genetic diseases.Nature reviews. Drug discovery · 2024
    Review
  12. Article
  13. Drug delivery systems for CRISPR-based genome editors.Nature reviews. Drug discovery · 2023
    Review
  14. Review
  15. Review
  16. Applications of synthetic biology in medical and pharmaceutical fields.Signal transduction and targeted therapy · 2023
    Review
  17. Review
  18. Article
  19. Review
  20. Potential of siRNA in COVID-19 therapy: Emphasis onFrontiers in bioengineering and biotechnology · 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

5 authors at 1 institution in 1 country.

Curtis DobrowolskiWallace H. Coulter Department of Biomedical Engineering, Georgia Institute of Technology and Emory University School of Medicine, Atlanta, GA, 30332, USA.
Kalina PaunovskaWallace H. Coulter Department of Biomedical Engineering, Georgia Institute of Technology and Emory University School of Medicine, Atlanta, GA, 30332, USA.
Marine Z C HatitWallace H. Coulter Department of Biomedical Engineering, Georgia Institute of Technology and Emory University School of Medicine, Atlanta, GA, 30332, USA.
Melissa P LokugamageWallace H. Coulter Department of Biomedical Engineering, Georgia Institute of Technology and Emory University School of Medicine, Atlanta, GA, 30332, USA.
James E DahlmanWallace H. Coulter Department of Biomedical Engineering, Georgia Institute of Technology and Emory University School of Medicine, Atlanta, GA, 30332, USA.ORCID 0000-0001-7580-436X
Georgia Institute of Technology · US

Funding

Highly Specific ZFN-Based HSC Gene Editing Therapies Identified By In Vivo Barcode Nanoparticle Screens And Rationally Designed MrnaUG3TR002855 · NCATS · GEORGIA INSTITUTE OF TECHNOLOGY · PI DAHLMAN, JAMES, SANTANGELO, PHILIP J · 2019 to 2021
$2.2M
Understanding the Relationship LNP Structure, Cholesterol Trafficking, and InVivo DeliveryR01GM132985 · NIGMS · GEORGIA INSTITUTE OF TECHNOLOGY · PI DAHLMAN, JAMES · 2019 to 2023
$2.0M
Highly Specific ZFN-Based HSC Gene Editing Therapies Identified By In Vivo Barcode Nanoparticle Screens And Rationally Designed MrnaUH3TR002855 · NCATS · EMORY UNIVERSITY · PI DAHLMAN, JAMES · 2022 to 2023
$1.3M
NCATS NIH HHS UG3 TR002855NCATS NIH HHS UH3 TR002855NIGMS NIH HHS R01 GM132985
6 · The paper itself

Abstract

RNA can alter the expression of endogenous genes and can be used to express therapeutic proteins. As a result, RNA-based therapies have recently mitigated disease in patients. Yet most potential RNA therapies cannot currently be developed, in large part because delivering therapeutic quantities of RNA drugs to diseased cells remains difficult. Here, recent studies focused on the biological hurdles that make in vivo drug delivery challenging are described. Then RNA drugs that have overcome these challenges in humans, focusing on siRNA to treat liver disease and mRNA to vaccinate against COVID, are discussed. Finally, research centered on improving drug delivery to new tissues is highlighted, including the development of high-throughput in vivo nanoparticle DNA barcoding assays capable of testing over 100 distinct nanoparticles in a single animal.

Indexed as

COVID-19NanoparticlesAnimalsDrug Delivery SystemsHumansLipidsRNA, Small InterferingSARS-CoV-2LipidsRNA, Small InterferingCOVIDin vivo deliveryLNPRNA therapyvaccine

Identifiers

PMID33661555
PMCPMC7995096
OpenAlexW3134278260

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.