Evidence map›Paper›PMID 38965378›Full record

ReviewNature reviews. Drug discovery2024

The 60-year evolution of lipid nanoparticles for nucleic acid delivery.

P R Cullis, P L Felgner

Abstract readReview
PubMed Publisher
In one paragraph

Review in Nature reviews. Drug discovery, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 249 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
249citing papers in PubMed, 1 pooled it
–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

249 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
  2. Article
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  5. Towards mRNA therapeutics 2.0.Nature reviews. Drug discovery · 2026
    Review
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  14. RNA therapeutics: current status and future directions.Signal transduction and targeted therapy · 2026
    Review
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  19. Review
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189 more citing papers are in PubMed but not listed here.

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

2 authors.

P R CullisDepartment of Biochemistry and Molecular Biology, University of British Columbia, Vancouver, British Columbia, Canada. pieterc@mail.ubc.ca.ORCID 0000-0001-9586-2508
P L FelgnerDepartment of Physiology & Biophysics, University of California, Irvine, CA, USA. pfelgner@hs.uci.edu.ORCID 0000-0002-4117-8505

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Delivery of genetic information to the interior of target cells in vivo has been a major challenge facing gene therapies. This barrier is now being overcome, owing in part to dramatic advances made by lipid-based systems that have led to lipid nanoparticles (LNPs) that enable delivery of nucleic acid-based vaccines and therapeutics. Examples include the clinically approved COVID-19 LNP mRNA vaccines and Onpattro (patisiran), an LNP small interfering RNA therapeutic to treat transthyretin-induced amyloidosis (hATTR). In addition, a host of promising LNP-enabled vaccines and gene therapies are in clinical development. Here, we trace this success to two streams of research conducted over the past 60 years: the discovery of the transfection properties of lipoplexes composed of positively charged cationic lipids complexed with nucleic acid cargos and the development of lipid nanoparticles using ionizable cationic lipids. The fundamental insights gained from these two streams of research offer potential delivery solutions for most forms of gene therapies.

Indexed as

Genetic TherapyLipidsNanoparticlesAnimalsCOVID-19COVID-19 VaccinesGene Transfer TechniquesHumansLiposomesNucleic AcidsRNA, Small InterferingCOVID-19 VaccinesLipid NanoparticlesLipidsLiposomesNucleic AcidsRNA, Small Interfering

Identifiers

What OpenQuestion holds

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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.