Evidence map›Paper›PMID 42337219›Full record

ArticleEuropean radiology experimental2026

Potentiation of the altered immune microenvironment following RF ablation of murine distant tumors with CTLA-4 immunotherapy.

Kun Zhao, Yuhan Shen, Wei Yang, Hao Wu, Bing Wang, Wenbo Wang, Wei Wu, Kun Yan, S Nahum Goldberg

Abstract read
In one paragraph

Article in European radiology experimental, 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
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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

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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

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0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

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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

9 authors.

Kun Zhao *Key Laboratory of Carcinogenesis and Translational Research (Ministry of Education/Beijing), Department of Ultrasound, Peking University Cancer Hospital & Institute, Beijing, China.
Yuhan Shen *Key Laboratory of Carcinogenesis and Translational Research (Ministry of Education/Beijing), Department of Ultrasound, Peking University Cancer Hospital & Institute, Beijing, China.
Wei YangKey Laboratory of Carcinogenesis and Translational Research (Ministry of Education/Beijing), Department of Ultrasound, Peking University Cancer Hospital & Institute, Beijing, China. 13681408183@163.com.ORCID http://orcid.org/0000-0003-1190-8068
Hao WuKey Laboratory of Carcinogenesis and Translational Research (Ministry of Education/Beijing), Department of Ultrasound, Peking University Cancer Hospital & Institute, Beijing, China.
Bing WangKey Laboratory of Carcinogenesis and Translational Research (Ministry of Education/Beijing), Department of Ultrasound, Peking University Cancer Hospital & Institute, Beijing, China.
Wenbo WangKey Laboratory of Carcinogenesis and Translational Research (Ministry of Education/Beijing), Department of Ultrasound, Peking University Cancer Hospital & Institute, Beijing, China.
Wei WuKey Laboratory of Carcinogenesis and Translational Research (Ministry of Education/Beijing), Department of Ultrasound, Peking University Cancer Hospital & Institute, Beijing, China.
Kun YanKey Laboratory of Carcinogenesis and Translational Research (Ministry of Education/Beijing), Department of Ultrasound, Peking University Cancer Hospital & Institute, Beijing, China.
S Nahum GoldbergDivision of Image-Guided Therapy, Department of Radiology, Hadassah Hebrew University Medical Center, Jerusalem, Israel. sgoldber@bidmc.harvard.edu.

Funding

Capital Foundation of Medical Development 2024-2-2157National Natural Science Foundation of China 82472002
6 · The paper itself

Abstract

objectivePrevious studies on the immune function after radiofrequency ablation (RFA) mainly focused on the immune microenvironment in residual tumors. Thus, we investigate the impact of complete RFA (cRFA) and incomplete RFA (iRFA) on the immune microenvironment of distant tumors, determining whether combination with immunotherapy can improve outcomes. MATERIALS AND MATERIALS: Using a bilateral subcutaneous CT26 murine model, one tumor underwent cRFA or iRFA while the contralateral tumor served as a distant site. Immune profiling by ribonucleic acid (RNA) sequencing, flow cytometry, and immunohistochemistry was performed at days 3 and 9 post-RFA (6 mice per group). Based on transcriptomic findings, anti-CTLA-4 therapy was evaluated following cRFA. Tumor growth and survival were additionally assessed (8 mice per group).

resultsInfiltration of CD8

conclusionComplete RFA is associated with a delayed immunosuppressive shift in distant tumors. Targeting CTLA-4 following ablation may partially mitigate this effect and enhance systemic tumor control. RELEVANCE STATEMENT: The combination of anti-CTLA-4 targeted therapy and complete radiofrequency ablation demonstrated a synergistic anti-tumor immunotherapy effect, which provided a potentially better therapeutic strategy for preventing tumor recurrence after radiofrequency ablation. KEY POINTS: The RNA-seq results demonstrated that CTLA-4 was upregulated in the distant tumor on 9 days after complete radiofrequency ablation. Anti-tumor immune response initially associated with radiofrequency ablation was relatively transient, while an immunosuppressive microenvironment was formed in the distant tumor in 9 days. Anti-CTLA-4 therapy after complete ablation significantly delayed distant tumor growth and promoted an anti-tumor immune microenvironment.

Indexed as

CTLA-4 AntigenImmunotherapyRadiofrequency AblationTumor MicroenvironmentAnimalsCell Line, TumorDisease Models, AnimalFemaleMiceMice, Inbred BALB CCTLA-4 AntigenCtla4 protein, mouseImmunotherapyMiceRadiofrequency ablationRNA-seqTumor microenvironment

Identifiers

PMID42337219
PMCPMC13291295

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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.