Evidence map›Paper›PMID 40027884›Full record

ArticleMolecular therapy. Nucleic acids2025

Yuta Suzuki, Takayuki Miyazaki, Yoko Ida, Tatsuya Suzuki, Yumi Itoh, Shuto Nakao, Keita Kondo, Kenji Kubara, Keisuke Nishioka, Hiroki Muto and 10 more

Abstract read
In one paragraph

Article in Molecular therapy. Nucleic acids, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Article
  2. 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

20 authors.

Yuta SuzukiTsukuba Research Laboratories, Eisai Co., Ltd., Ibaraki 300-2635, Japan.
Takayuki MiyazakiTsukuba Research Laboratories, Eisai Co., Ltd., Ibaraki 300-2635, Japan.
Yoko IdaKobe Research Laboratories, Eisai Co., Ltd., Kobe 650-0047, Japan.
Tatsuya SuzukiDepartment of Microbiology, Juntendo University School of Medicine, Tokyo 113-8421, Japan.
Yumi ItohDepartment of Microbiology, Juntendo University School of Medicine, Tokyo 113-8421, Japan.
Shuto NakaoDepartment of Microbiology, Juntendo University School of Medicine, Tokyo 113-8421, Japan.
Keita KondoTsukuba Research Laboratories, Eisai Co., Ltd., Ibaraki 300-2635, Japan.
Kenji KubaraTsukuba Research Laboratories, Eisai Co., Ltd., Ibaraki 300-2635, Japan.
Keisuke NishiokaDepartment of Infectious Diseases, Graduate School of Medical Science, Kyoto Prefectural University of Medicine, Kyoto 602-8566, Japan.
Hiroki MutoTsukuba Research Laboratories, Eisai Co., Ltd., Ibaraki 300-2635, Japan.
Ryuji WatariTsukuba Research Laboratories, Eisai Co., Ltd., Ibaraki 300-2635, Japan.
Toshifumi HirayamaKobe Research Laboratories, Eisai Co., Ltd., Kobe 650-0047, Japan.
Dai KakiuchiTsukuba Research Laboratories, Eisai Co., Ltd., Ibaraki 300-2635, Japan.
Shinya SatoTsukuba Research Laboratories, Eisai Co., Ltd., Ibaraki 300-2635, Japan.
Satoshi InoueTsukuba Research Laboratories, Eisai Co., Ltd., Ibaraki 300-2635, Japan.
Yoshifumi UemotoTsukuba Research Laboratories, Eisai Co., Ltd., Ibaraki 300-2635, Japan.
Yohei MukaiKobe Research Laboratories, Eisai Co., Ltd., Kobe 650-0047, Japan.
Atsushi HoshinoDepartment of Cardiovascular Medicine, Graduate School of Medical Science, Kyoto Prefectural University of Medicine, Kyoto 602-8566, Japan.
Toru OkamotoDepartment of Microbiology, Juntendo University School of Medicine, Tokyo 113-8421, Japan.
Junji MatsuiTsukuba Research Laboratories, Eisai Co., Ltd., Ibaraki 300-2635, Japan.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Severe acute respiratory syndrome coronavirus-2 (SARS-CoV-2) variants repeatedly evade the immune system within short periods. Thus, next-generation therapeutics that are resistant to mutations and can be rapidly supplied to individuals in an emergency are required. Here, we designed an mRNA encoding an engineered angiotensin-converting enzyme 2 (ACE2) decoy, 3N39v4, composed of high-affinity ACE2 and a human immunoglobulin G Fc domain. The 3N39v4-encoded mRNA was encapsulated in lipid nanoparticles for efficient

Indexed as

ACE2 decoyCOVID-19escape mutationlipid nanoparticlesmRNA deliverymRNA therapeuticsMT: Oligonucleotides: Therapies and ApplicationsSARS-CoV-2

Identifiers

PMID40027884
PMCPMC11869860

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.