Evidence map›Paper›PMID 34589288›Full record

ArticleMolecular therapy. Nucleic acids2021

Wataru Kawase, Daisuke Kurotaki, Yuta Suzuki, Hiroshi Ishihara, Tatsuma Ban, Go R Sato, Juri Ichikawa, Hideyuki Yanai, Tadatsugu Taniguchi, Kappei Tsukahara and 1 more

Open access · goldAbstract read
In one paragraph

Article in Molecular therapy. Nucleic acids, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
1.1field-weighted citation impact, top 22% 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

11 citing papers in PubMed, 20 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Article
  5. Molecular therapy. Nucleic acids · 2025
    Article
  6. Lymph node macrophages drive innate immune responses to enhance the anti-tumor efficacy of mRNA vaccines.Molecular therapy : the journal of the American Society of Gene Therapy · 2024
    Article
  7. Article
  8. Article
  9. Nonviral nanoparticle gene delivery into the CNS for neurological disorders and brain cancer applications.Wiley interdisciplinary reviews. Nanomedicine and nanobiotechnology · 2023
    Review
  10. Article
  11. 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

11 authors at 3 institutions in 1 country.

Wataru KawaseDepartment of Immunology, Yokohama City University Graduate School of Medicine, Yokohama 236-0004, Japan.
Daisuke KurotakiDepartment of Immunology, Yokohama City University Graduate School of Medicine, Yokohama 236-0004, Japan.
Yuta SuzukiTsukuba Research Laboratories, Eisai Co., Ltd, Tsukuba 300-2635, Japan.
Hiroshi IshiharaTsukuba Research Laboratories, Eisai Co., Ltd, Tsukuba 300-2635, Japan.
Tatsuma BanDepartment of Immunology, Yokohama City University Graduate School of Medicine, Yokohama 236-0004, Japan.
Go R SatoDepartment of Immunology, Yokohama City University Graduate School of Medicine, Yokohama 236-0004, Japan.
Juri IchikawaDepartment of Immunology, Yokohama City University Graduate School of Medicine, Yokohama 236-0004, Japan.
Hideyuki YanaiDepartment of Inflammology, Research Center for Advanced Science and Technology, The University of Tokyo, Tokyo 153-0041, Japan.
Tadatsugu TaniguchiDepartment of Inflammology, Research Center for Advanced Science and Technology, The University of Tokyo, Tokyo 153-0041, Japan.
Kappei TsukaharaTsukuba Research Laboratories, Eisai Co., Ltd, Tsukuba 300-2635, Japan.
Tomohiko TamuraDepartment of Immunology, Yokohama City University Graduate School of Medicine, Yokohama 236-0004, Japan.
Yokohama City University · JPEisai (Japan) · JPThe University of Tokyo · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

RNA interference-based gene silencing drugs are attracting attention for treating various diseases. Lipid nanoparticles (LNPs) are carriers that efficiently deliver small interfering RNA (siRNA) to the cytoplasm of target cells. Recently, we developed potent and well-tolerated biodegradable LNPs with asymmetric ionizable lipids. Here, we evaluated the effect of LNPs on immune cells in mice. After intravenous administration, LNPs were efficiently incorporated into several tissue-resident macrophages, including liver macrophages, through an apolipoprotein E (ApoE)-independent mechanism. Administration of LNP-encapsulated siRNA against

Indexed as

drug delivery systemhepatitisIRF5lipid nanoparticlesmacrophagessiRNA

Identifiers

PMID34589288
PMCPMC8463440
OpenAlexW3199618457

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.