Evidence map›Paper›PMID 41603157›Full record

ArticleAdvanced science (Weinheim, Baden-Wurttemberg, Germany)2026

Non-Targeting shRNA-Encoded Plasmid DNA Enhances Protective Immunity Through RIDD-RIG-I Signaling Pathway in the Zika Virus Animal Model.

Min-Syuan Huang, Hung-Chun Liao, Po Peng, Wan-Ling Wu, Kit Man Chai, Mei-Yu Chen, Guann-Yi Yu, Tsung-Hsien Chuang, Hsin-Wei Chen, Chuang-Rung Chang and 1 more

Abstract read
In one paragraph

Article in Advanced science (Weinheim, Baden-Wurttemberg, Germany), 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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.

Min-Syuan HuangNational Institute of Infectious Disease and Vaccinology, National Health Research Institutes, Miaoli, Taiwan.
Hung-Chun LiaoNational Institute of Infectious Disease and Vaccinology, National Health Research Institutes, Miaoli, Taiwan.
Po PengWelgene Biotech. Co., Ltd., Taipei, Taiwan.
Wan-Ling WuNational Institute of Infectious Disease and Vaccinology, National Health Research Institutes, Miaoli, Taiwan.
Kit Man ChaiNational Institute of Infectious Disease and Vaccinology, National Health Research Institutes, Miaoli, Taiwan.
Mei-Yu ChenNational Institute of Infectious Disease and Vaccinology, National Health Research Institutes, Miaoli, Taiwan.
Guann-Yi YuNational Institute of Infectious Disease and Vaccinology, National Health Research Institutes, Miaoli, Taiwan.
Tsung-Hsien ChuangImmunology Research Center, National Health Research Institutes, Miaoli, Taiwan.
Hsin-Wei ChenNational Institute of Infectious Disease and Vaccinology, National Health Research Institutes, Miaoli, Taiwan.
Chuang-Rung ChangInstitute of Biotechnology, College of Life Science and Medicine, National Tsing Hua University, Hsinchu, Taiwan.
Shih-Jen LiuNational Institute of Infectious Disease and Vaccinology, National Health Research Institutes, Miaoli, Taiwan.ORCID https://orcid.org/0000-0002-8736-1452

Funding

National Health Research Institutes IV-111-GP-06National Health Research Institutes IV-113-PP-17National Science and Technology Council 111-2314-B-400 -041 -MY3National Science and Technology Council 114-2740-B-400-004
6 · The paper itself

Abstract

DNA vaccines offer advantages such as low production cost, rapid manufacturing, and enhanced stability for transport and storage, making them suitable for addressing tropical and emerging infectious diseases. However, their limited immunogenicity in humans often necessitates multiple booster doses or high antigen quantities, posing a significant barrier to broader application. To overcome this limitation, we developed a DNA vaccine encoding the Zika virus (ZIKV) structural proteins (prME) that incorporates a non-targeting short hairpin RNA (shRNA) as an intrinsic molecular adjuvant. This shRNA is not designed to silence host genes; rather, it enhances innate immune "RIG-I" signaling by selectively activating the IRE1α-dependent regulated IRE1-dependent decay pathway. Mechanistically, shRNA overexpression is inferred to increase the load on the RNA-induced silencing complex, potentially triggering IRE1α oligomerization and subsequent upregulation of TXNIP. These events generate cytoplasmic RNA fragments that activate RIG-I and downstream antiviral responses. In murine models, the vaccine elicited strong ZIKV-specific humoral and cellular immune responses. In AGB6 mice, it significantly increased neutralizing antibody titers, reduced viremia, and improved survival. This approach enhances the immunogenicity of DNA vaccines without targeting host genes, providing a scalable and adaptable platform for infectious disease prevention.

Indexed as

DEAD Box Protein 58PlasmidsRNA, Small InterferingVaccines, DNAZika VirusZika Virus InfectionAnimalsDisease Models, AnimalFemaleHumansMiceSignal TransductionDEAD Box Protein 58RNA, Small InterferingVaccines, DNAimmunogenicitymolecular adjuvantsnon‐targeting shRNAregulated IRE1‐dependent decay (RIDD) pathwayZika virus

Identifiers

PMID41603157
PMCPMC13045247

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.