Evidence map›Paper›PMID 36835091›Full record

ReviewInternational journal of molecular sciences2023

The Dilemma of HSV-1 Oncolytic Virus Delivery: The Method Choice and Hurdles.

Guijin Tang, Dawei Wang, Xiangqian Zhao, Zhihua Feng, Qi Chen, Yangkun Shen

Abstract readReview
In one paragraph

Review in International journal of molecular sciences, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 30 papers.

0numbers the graph read from it
0cells of the map it votes in
30citing 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

30 citing papers in PubMed.

  1. Review
  2. Cell death network regulation in HSV infection: immune evasion versus host defense.Apoptosis : an international journal on programmed cell death · 2026
    Review
  3. Review
  4. Review
  5. Review
  6. Review
  7. Oncolytic human herpesvirus for cancer therapy.Molecular biology reports · 2026
    Review
  8. Cancer viroimmunotherapy platforms based on varicella-zoster virus and cytomegalovirus.Molecular therapy : the journal of the American Society of Gene Therapy · 2026
    Review
  9. Article
  10. Review
  11. Article
  12. Review
  13. Article
  14. Review
  15. Article
  16. Review
  17. Review
  18. Review
  19. Review
  20. CRISPR-Mediated Viral Gene Knock-In for Studying Viral-Host Interactions.Methods in molecular biology (Clifton, N.J.) · 2025
    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

6 authors.

Guijin TangFujian Key Laboratory of Innate Immune Biology, Biomedical Research Center of South China, Qishan Campus, Fujian Normal University, College Town, Fuzhou 350117, China.
Dawei WangFujian Key Laboratory of Innate Immune Biology, Biomedical Research Center of South China, Qishan Campus, Fujian Normal University, College Town, Fuzhou 350117, China.
Xiangqian ZhaoFujian Key Laboratory of Innate Immune Biology, Biomedical Research Center of South China, Qishan Campus, Fujian Normal University, College Town, Fuzhou 350117, China.
Zhihua FengFujian Key Laboratory of Innate Immune Biology, Biomedical Research Center of South China, Qishan Campus, Fujian Normal University, College Town, Fuzhou 350117, China.
Qi ChenFujian Key Laboratory of Innate Immune Biology, Biomedical Research Center of South China, Qishan Campus, Fujian Normal University, College Town, Fuzhou 350117, China.ORCID 0000-0001-9063-6819
Yangkun ShenFujian Key Laboratory of Innate Immune Biology, Biomedical Research Center of South China, Qishan Campus, Fujian Normal University, College Town, Fuzhou 350117, China.

Funding

the Natural Science Foundation of Fujian Province, China 2022J01652
6 · The paper itself

Abstract

Oncolytic viruses (OVs) have emerged as effective gene therapy and immunotherapy drugs. As an important gene delivery platform, the integration of exogenous genes into OVs has become a novel path for the advancement of OV therapy, while the herpes simplex virus type 1 (HSV-1) is the most commonly used. However, the current mode of administration of HSV-1 oncolytic virus is mainly based on the tumor in situ injection, which limits the application of such OV drugs to a certain extent. Intravenous administration offers a solution to the systemic distribution of OV drugs but is ambiguous in terms of efficacy and safety. The main reason is the synergistic role of innate and adaptive immunity of the immune system in the response against the HSV-1 oncolytic virus, which is rapidly cleared by the body's immune system before it reaches the tumor, a process that is accompanied by side effects. This article reviews different administration methods of HSV-1 oncolytic virus in the process of tumor treatment, especially the research progress in intravenous administration. It also discusses immune constraints and solutions of intravenous administration with the intent to provide new insights into HSV-1 delivery for OV therapy.

Indexed as

Herpesvirus 1, HumanNeoplasmsOncolytic VirotherapyOncolytic VirusesAdaptive ImmunityHumanscancer immunotherapyherpes simplex virus type 1HSV-1 oncolytic virus therapyintravenous injectionmode of administrationoncolytic virus

Identifiers

PMID36835091
PMCPMC9962028

What OpenQuestion holds

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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.