Evidence map›Paper›PMID 39256822›Full record

ReviewJournal of biomedical science2024

Current landscape of mRNA technologies and delivery systems for new modality therapeutics.

Ruei-Min Lu, Hsiang-En Hsu, Ser John Lynon P Perez, Monika Kumari, Guan-Hong Chen, Ming-Hsiang Hong, Yin-Shiou Lin, Ching-Hang Liu, Shih-Han Ko, Christian Angelo P Concio and 4 more

Abstract readReview
In one paragraph

Review in Journal of biomedical science, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 48 papers.

0numbers the graph read from it
0cells of the map it votes in
48citing 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

48 citing papers in PubMed.

  1. Review
  2. Review
  3. Review
  4. Review
  5. Article
  6. Article
  7. Article
  8. Article
  9. Article
  10. Review
  11. Review
  12. Review
  13. Review
  14. Review
  15. Review
  16. Review
  17. Article
  18. Uncovering cancer dependencies in peptide-interacting protein pockets.bioRxiv : the preprint server for biology · 2026
    Article
  19. Review
  20. 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

14 authors.

Ruei-Min LuBiomedical Translation Research Center, Academia Sinica, Taipei, 11571, Taiwan.
Hsiang-En HsuBiomedical Translation Research Center, Academia Sinica, Taipei, 11571, Taiwan.
Ser John Lynon P PerezBiomedical Translation Research Center, Academia Sinica, Taipei, 11571, Taiwan.
Monika KumariInstitute of Cellular and Organismic Biology, Academia Sinica, No. 128, Academia Road, Section 2, Taipei, 11529, Taiwan.
Guan-Hong ChenBiomedical Translation Research Center, Academia Sinica, Taipei, 11571, Taiwan.
Ming-Hsiang HongBiomedical Translation Research Center, Academia Sinica, Taipei, 11571, Taiwan.
Yin-Shiou LinBiomedical Translation Research Center, Academia Sinica, Taipei, 11571, Taiwan.
Ching-Hang LiuBiomedical Translation Research Center, Academia Sinica, Taipei, 11571, Taiwan.
Shih-Han KoBiomedical Translation Research Center, Academia Sinica, Taipei, 11571, Taiwan.
Christian Angelo P ConcioInstitute of Chemistry, Academia Sinica, No. 128, Academia Road, Section 2, Taipei, 11529, Taiwan.
Yi-Jen SuInstitute of Cellular and Organismic Biology, Academia Sinica, No. 128, Academia Road, Section 2, Taipei, 11529, Taiwan.
Yi-Han ChangBiomedical Translation Research Center, Academia Sinica, Taipei, 11571, Taiwan.
Wen-Shan LiBiomedical Translation Research Center, Academia Sinica, Taipei, 11571, Taiwan. wenshan@gate.sinica.edu.tw.
Han-Chung WuBiomedical Translation Research Center, Academia Sinica, Taipei, 11571, Taiwan. hcw0928@gate.sinica.edu.tw.ORCID http://orcid.org/0000-0002-5185-1169

Funding

Academia Sinica AS-KPQ-110-EIMDAcademia Sinica AS-KPQ-111-KNT
6 · The paper itself

Abstract

Realizing the immense clinical potential of mRNA-based drugs will require continued development of methods to safely deliver the bioactive agents with high efficiency and without triggering side effects. In this regard, lipid nanoparticles have been successfully utilized to improve mRNA delivery and protect the cargo from extracellular degradation. Encapsulation in lipid nanoparticles was an essential factor in the successful clinical application of mRNA vaccines, which conclusively demonstrated the technology's potential to yield approved medicines. In this review, we begin by describing current advances in mRNA modifications, design of novel lipids and development of lipid nanoparticle components for mRNA-based drugs. Then, we summarize key points pertaining to preclinical and clinical development of mRNA therapeutics. Finally, we cover topics related to targeted delivery systems, including endosomal escape and targeting of immune cells, tumors and organs for use with mRNA vaccines and new treatment modalities for human diseases.

Indexed as

Drug Delivery SystemsNanoparticlesRNA, MessengerHumansLipidsLiposomesmRNA VaccinesLipid NanoparticlesLipidsLiposomesmRNA VaccinesRNA, MessengerLipid nanoparticlesmRNA TechnologymRNA therapeuticsNew modality therapeuticsTargeting mRNA delivery systems

Identifiers

PMID39256822
PMCPMC11389359

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.