Evidence map›Paper›PMID 39567771›Full record

ArticleCancer gene therapy2025

Oncolytic virus encoding 4-1BBL and IL15 enhances the efficacy of tumor-infiltrating lymphocyte adoptive therapy in HCC.

Kai Ye, Yongfeng Yan, Rui Su, Qinghai Dai, Kunyan Qiao, Yu Cao, Jian Xu, Lihua Yan, Zhixiao Huo, Wei Liu and 4 more

Abstract read
PubMed Publisher
In one paragraph

Article in Cancer gene therapy, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

3 citing papers in PubMed.

  1. Review
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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

14 authors.

Kai Ye *Clinical School of the Second People's Hospital, Tianjin Medical University, Tianjin, China.
Yongfeng Yan *Department of Laboratory, Tianjin Beichen Hospital, Tianjin, China.
Rui SuClinical School of the Second People's Hospital, Tianjin Medical University, Tianjin, China. surui831109@126.com.
Qinghai DaiClinical School of the Second People's Hospital, Tianjin Medical University, Tianjin, China.
Kunyan QiaoClinical School of the Second People's Hospital, Tianjin Medical University, Tianjin, China.
Yu CaoClinical School of the Second People's Hospital, Tianjin Medical University, Tianjin, China.
Jian XuClinical School of the Second People's Hospital, Tianjin Medical University, Tianjin, China.
Lihua YanClinical School of the Second People's Hospital, Tianjin Medical University, Tianjin, China.
Zhixiao HuoClinical School of the Second People's Hospital, Tianjin Medical University, Tianjin, China.
Wei LiuClinical School of the Second People's Hospital, Tianjin Medical University, Tianjin, China.
Yue HuClinical School of the Second People's Hospital, Tianjin Medical University, Tianjin, China.
Yu ZhuDepartment of Clinical Laboratory, The Third Central Hospital of Tianjin, Tianjin Key Laboratory of Extracorporeal Life Support for Critical Diseases, Artificial Cell Engineering Technology Research Center, Tianjin Institute of Hepatobiliary Disease, Tianjin, China. zhuyutj@126.com.
Liang XuClinical School of the Second People's Hospital, Tianjin Medical University, Tianjin, China. xuyangliang2004@sina.com.
Yuqiang MiClinical School of the Second People's Hospital, Tianjin Medical University, Tianjin, China. yuqiangmi68@163.com.ORCID 0000-0001-7809-2679

Funding

Natural Science Foundation of Tianjin City (Natural Science Foundation of Tianjin) 23JCYBJC00950Tianjin Municipal Education Commission 2023KJ015
6 · The paper itself

Abstract

Previous studies have found that oncolytic virus (OVs) can improve the efficacy of TIL adoptive therapy in oral cancer, colon cancer, and pancreatic cancer. However, the curative effect in hepatocellular carcinoma (HCC) is still unclear. Therefore, this study aims to explore the therapeutic effect and mechanism of OVs encoding 4-1BBL and IL15 (OV-4-1BBL/IL15) combined with TIL adoptive therapy on HCC. In this study, the role and immunological mechanism of armed OVs combined with TILs were evaluated by flow cytometry and ELISA in patient-derived xenograft and syngeneic mouse tumor models. Co-culturing with TILs can up-regulate the expression of antigen-presenting cell (APC) markers on the surface of OV-infected primary HCC cells, and promote the specific activation ability and tumor-killing ability of TILs. OV-4-1BBL/IL15 combined with TIL adoptive therapy could induce tumor volume reduction and anti-tumor immune memory in patient-derived xenograft and syngeneic mouse tumor models. Furthermore, OV combined with TIL adoptive therapy can endow tumor cells with aAPC characteristics, activate T cells at the same time, and reprogram tumor macrophages into anti-tumor phenotype. OV-4-1BBL/IL15 can stimulate the anti-tumor potential of TIL therapy in HCC, and possess broad clinical application prospects.

Indexed as

4-1BB LigandCarcinoma, HepatocellularImmunotherapy, AdoptiveInterleukin-15Liver NeoplasmsLymphocytes, Tumor-InfiltratingOncolytic VirotherapyOncolytic VirusesAnimalsCell Line, TumorDisease Models, AnimalFemaleHumansMiceXenograft Model Antitumor Assays4-1BB LigandIL15 protein, humanInterleukin-15

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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.