Evidence map›Paper›PMID 39631848›Full record

ArticleJournal for immunotherapy of cancer2024

Durable antitumor response via an oncolytic virus encoding decoy-resistant IL-18.

Yan Cheng, Yuanhui Zhao, Yu Liu, Yichi Zhang, Dongge Xu, Weikang Sun, Mengyu Zhang, Yuqing Miao, Susu He, Yayi Hou and 2 more

Abstract read
In one paragraph

Article in Journal for immunotherapy of cancer, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing 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

8 citing papers in PubMed.

  1. Article
  2. Review
  3. Review
  4. Article
  5. Article
  6. Article
  7. Article
  8. NK cells in HPV-related tumorigenesis: mechanisms and clinical applications.Frontiers in cellular and infection microbiology · 2025
    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

12 authors.

Yan ChengState Key Laboratory of Biotechnology, Medical School, Nanjing University, Nanjing, China.
Yuanhui ZhaoState Key Laboratory of Biotechnology, Medical School, Nanjing University, Nanjing, China.
Yu LiuShanghai No. 10 Peoples Hospital, Shanghai, China.
Yichi ZhangMoores Cancer Center, University of California San Diego, La Jolla, California, USA.
Dongge XuState Key Laboratory of Biotechnology, Medical School, Nanjing University, Nanjing, China.
Weikang SunState Key Laboratory of Biotechnology, Medical School, Nanjing University, Nanjing, China.
Mengyu ZhangState Key Laboratory of Biotechnology, Medical School, Nanjing University, Nanjing, China.
Yuqing MiaoJiangsu Key Laboratory of Molecular Medicine, Medical School, Nanjing University, Nanjing, China.
Susu HeState Key Laboratory of Biotechnology, Medical School, Nanjing University, Nanjing, China.
Yayi HouState Key Laboratory of Biotechnology, Medical School, Nanjing University, Nanjing, China.ORCID 0000-0002-1152-9132
Dwayne StupackMoores Cancer Center, University of California San Diego, La Jolla, California, USA dstupack@ucsd.edu erguang@nju.edu.cn.ORCID 0000-0003-4396-5745
Erguang LiState Key Laboratory of Biotechnology, Medical School, Nanjing University, Nanjing, China dstupack@ucsd.edu erguang@nju.edu.cn.ORCID 0000-0002-3065-1336

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundInterleukin-18 (IL-18), or interferon (IFN)-γ-inducing factor, potentiates T helper 1 and natural killer cell activation as well as CD8

methodsoAd harboring wild-type IL-18 or DR18 (oAdDR18) was constructed by inserting IL-18 mutant into modified oAd backbone with Ad5/3 chimeric fiber. The delivery effect and IFN-γ induction were determined by ELISA. The antitumor efficiency of oAdDR18 was tested in CT26, B16BL6 and 4T1 tumor-bearing mice, or athymic nude mice and compared with recombinant DR18 protein (rDR18). 4T1 lung metastasis model was used to evaluate the antitumor efficiency of local and distant tumors. Antitumor memory and synergistic effect with an anti-programmed cell death protein-1 (PD-1) antibody was evaluated. The phenotypes of the immune cells in tumor microenvironment were analyzed by flow cytometry and immunohistochemistry.

resultsMice received oAdDR18 maintained stable production of IL-18 and IFN-γ compared with those received rDR18. Intratumoral delivery of oAdDR18 significantly reduced tumor growth across several tumor models, but not in the athymic nude mouse model. Mice that had tumor remission showed antitumor memory. The antitumor effect was associated with intratumor infiltration of CD4

conclusionsoAdDR18 demonstrates enhanced antitumor activities through the induction of stronger local and system immunities and modulation of the tumor microenvironment compared with those of oAdwtIL-18 and rDR18. A combination of oncolytic virotherapy with cytokine engineering would lead to cytokine-based therapeutics for cancer and other diseases.

Indexed as

Interleukin-18Oncolytic VirusesAnimalsCell Line, TumorFemaleHumansLung NeoplasmsMiceMice, NudeOncolytic VirotherapyTumor MicroenvironmentInterleukin-18AbscopalCytokineIntratumoralOncolytic virusT cell

Identifiers

PMID39631848
PMCPMC11624705

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.