Evidence map›Paper›PMID 29526650›Full record

ArticleMolecular therapy : the journal of the American Society of Gene Therapy2018

miRNAs Targeting ICP4 and Delivered to Susceptible Cells in Exosomes Block HSV-1 Replication in a Dose-Dependent Manner.

Lei Wang, Xiaoqing Chen, Xusha Zhou, Bernard Roizman, Grace Guoying Zhou

Abstract read
In one paragraph

Article in Molecular therapy : the journal of the American Society of Gene Therapy, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing 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

14 citing papers in PubMed.

  1. Article
  2. Viruses and neurodegeneration: a growing concern.Journal of translational medicine · 2025
    Review
  3. Article
  4. Article
  5. Review
  6. Review
  7. Article
  8. Article
  9. Extracellular Vesicles Regulated by Viruses and Antiviral Strategies.Frontiers in cell and developmental biology · 2021
    Review
  10. Article
  11. Article
  12. Article
  13. Review
  14. Cloaked Viruses and Viral Factors in Cutting Edge Exosome-Based Therapies.Frontiers in cell and developmental biology · 2020
    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

5 authors.

Lei WangSchool of Basic Medical Sciences, Guangzhou Medical University, Guangzhou, Guangdong 511436, China.
Xiaoqing ChenShenzhen International Institute for Biomedical Research, Dapeng New District, Shenzhen, Guangdong 518116, China.
Xusha ZhouSchool of Basic Medical Sciences, Guangzhou Medical University, Guangzhou, Guangdong 511436, China.
Bernard RoizmanShenzhen International Institute for Biomedical Research, Dapeng New District, Shenzhen, Guangdong 518116, China; Cummings Life Sciences Center, The University of Chicago, Chicago, IL 60637, USA. Electronic address: bernard.roizman@bsd.uchicago.edu.
Grace Guoying ZhouSchool of Basic Medical Sciences, Guangzhou Medical University, Guangzhou, Guangdong 511436, China; Shenzhen International Institute for Biomedical Research, Dapeng New District, Shenzhen, Guangdong 518116, China. Electronic address: zhoug@siitm.org.cn.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

miRNAs are potent tools that in principle can be used to control the replication of infectious agents. The objectives of the studies reported here were to design miRNAs that can block the replication of herpes simplex virus 1 and which could be delivered to infected cells via exosomes. We report the following: (1) We designed three miRNAs targeting the mRNA encoding ICP4, an essential viral regulatory protein. Of the three miRNAs, one miRNA401 effectively blocked ICP4 accumulation and viral replication on transfection into susceptible cells. (2) To facilitate packaging of the miRNA into exosomes, we incorporated into the sequence of miRNA401 an exosome-packaging motif. miRNA401 was shown to be packaged into exosomes and successfully delivered by exosomes to susceptible cells, where it remained stable for at least 72 hr. Finally, the results show that miRNA401 delivered to cells via exosomes effectively reduced virus yields in a miRNA401 dose-dependent fashion. The protocol described in this report can be applied to study viral gene functions without actually deleting or mutagenizing the gene.

Indexed as

Gene Expression Regulation, ViralRNA InterferenceVirus ReplicationCells, CulturedExosomesGenetic VectorsHerpes SimplexHerpesvirus 1, HumanHumansImmediate-Early ProteinsMicroRNAsRNA Transportherpes simplex virus IE3 protein, Human herpesvirus 1Immediate-Early ProteinsMicroRNAsexosomeHSV-1target miRNAviral replication

Identifiers

PMID29526650
PMCPMC6080130

What OpenQuestion holds

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Registered trials

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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.