Evidence map›Paper›PMID 41102346›Full record

ReviewNature biomedical engineering2025

Targeting and tracking mRNA lipid nanoparticles at the particle, transcript and protein level.

Diana D Kang, Adam Marks, Judit Morla-Folch, Yizhou Dong, Brian D Brown, Abraham J P Teunissen

Abstract readReview
In one paragraph

Review in Nature biomedical engineering, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing 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

13 citing papers in PubMed.

  1. Genes & diseases · 2027
    Review
  2. Article
  3. Review
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  6. Review
  7. Article
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  10. 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

6 authors.

Diana D Kang *Icahn Genomics Institute, Icahn School of Medicine at Mount Sinai, New York, NY, USA.
Adam Marks *Icahn Genomics Institute, Icahn School of Medicine at Mount Sinai, New York, NY, USA.
Judit Morla-FolchIcahn Genomics Institute, Icahn School of Medicine at Mount Sinai, New York, NY, USA.
Yizhou DongIcahn Genomics Institute, Icahn School of Medicine at Mount Sinai, New York, NY, USA. yizhou.dong@mssm.edu.ORCID http://orcid.org/0000-0001-5786-0659
Brian D BrownIcahn Genomics Institute, Icahn School of Medicine at Mount Sinai, New York, NY, USA. brian.brown@mssm.edu.ORCID http://orcid.org/0000-0002-3670-8778
Abraham J P TeunissenIcahn Genomics Institute, Icahn School of Medicine at Mount Sinai, New York, NY, USA. bram.teunissen@mssm.edu.ORCID http://orcid.org/0000-0002-0401-8262

Funding

Translational imaging and nanomedicine in inflammatory atherosclerosisP01HL131478 · NHLBI · ICAHN SCHOOL OF MEDICINE AT MOUNT SINAI · PI Zahi A. Fayad · 2017 to 2026
$24.3M
Using trained immunity-inhibiting nanobiologics to achieve tolerance of heart allografts in non-human primatesP01AI168258 · NIAID · ICAHN SCHOOL OF MEDICINE AT MOUNT SINAI · PI Zahi A. Fayad, Joren C Madsen · 2023 to 2026
$14.7M
Spatial functional genomics to identify regulators of the tumor microenvironment and cancer immunityU01CA282114 · NCI · ICAHN SCHOOL OF MEDICINE AT MOUNT SINAI · PI Brian D Brown, MIRIAM MERAD · 2023 to 2026
$4.2M
Integration of adjuvant derived nanoparticles and engineered mRNA for HIV vaccine discoveryR01AI174902 · NIAID · ICAHN SCHOOL OF MEDICINE AT MOUNT SINAI · PI Yizhou Dong, Darrell J Irvine · 2023 to 2026
$3.2M
Construction of in vivo mRNA delivery systemsR35GM144117 · NIGMS · OHIO STATE UNIVERSITY · PI Yizhou Dong · 2022 to 2026
$2.4M
microRNA-controlled mRNA therapeuticsR01DK138025 · NIDDK · ICAHN SCHOOL OF MEDICINE AT MOUNT SINAI · PI Brian D Brown · 2024 to 2026
$1.7M
NCI NIH HHS U01 CA282114NHLBI NIH HHS P01 HL131478NIAID NIH HHS P01 AI168258NIAID NIH HHS R01 AI174902NIDDK NIH HHS R01 DK138025NIGMS NIH HHS R35 GM144117U.S. Department of Health & Human Services | NIH | National Heart, Lung, and Blood Institute (NHLBI) 2P01HL131478-06A1U.S. Department of Health & Human Services | NIH | National Institute of Allergy and Infectious Diseases (NIAID) 1P01AI168258-01
6 · The paper itself

Abstract

Lipid nanoparticles (LNPs) are a versatile platform with numerous experimental, diagnostic and therapeutic applications. However, the high propensity of LNPs to accumulate in hepatocytes and antigen-presenting cells has largely limited their clinical use to vaccines and the treatment of liver diseases. In this Review, we describe established and emerging techniques for monitoring the in vivo behaviour of RNA-loaded LNPs (RNA-LNPs) and strategies for improved tissue and cell targeting that expand the applications of this technology. We discuss innovations in LNP chemistry and bioengineering, and exploiting synthetic biology to tailor the cellular expression of the mRNA cargo, including the use of microRNA target sites. We also review how modifications to the encoded protein can be used to control stability and subcellular localization of the payload. Lastly, we discuss how these techniques and strategies can accelerate the clinical translation of RNA-LNP drugs and improve therapeutic outcomes.

Indexed as

LipidsNanoparticlesProteinsRNA, MessengerAnimalsDrug Delivery SystemsHumansLiposomesMicroRNAsLipid NanoparticlesLipidsLiposomesMicroRNAsProteinsRNA, Messenger

Identifiers

PMID41102346
PMCPMC12673502

What OpenQuestion holds

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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.