Evidence map›Paper›PMID 39981234›Full record

ArticleFrontiers in immunology2025

Ddx21 mutant peptide is an effective neoantigen in prophylactic lung cancer vaccines and activates long-term anti-tumor immunity.

Zhe Zhang, Yimeng Xia, Zhihong Wang, Yaxing Sun, Dan Pu, Yijia He, Ruixian Liu, Yanru Zhang, Yan Liu, Junzhi Yu and 4 more

Abstract read
In one paragraph

Article in Frontiers in immunology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. 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

14 authors.

Zhe Zhang *Department of Gastroenterology, the Second Affiliated Hospital of Zhengzhou University, Zhengzhou, China.
Yimeng Xia *Department of Gastroenterology, the Second Affiliated Hospital of Zhengzhou University, Zhengzhou, China.
Zhihong WangDepartment of Gastroenterology, the Second Affiliated Hospital of Zhengzhou University, Zhengzhou, China.
Yaxing SunDepartment of Gastroenterology, the Second Affiliated Hospital of Zhengzhou University, Zhengzhou, China.
Dan PuDepartment of Gastroenterology, the Second Affiliated Hospital of Zhengzhou University, Zhengzhou, China.
Yijia HeDepartment of Microbiology and Immunology, School of Basic Medical Sciences, Zhengzhou University, Zhengzhou, China.
Ruixian LiuDepartment of Gastroenterology, the Second Affiliated Hospital of Zhengzhou University, Zhengzhou, China.
Yanru ZhangDepartment of Gastroenterology, the Second Affiliated Hospital of Zhengzhou University, Zhengzhou, China.
Yan LiuDepartment of Gastroenterology, the Second Affiliated Hospital of Zhengzhou University, Zhengzhou, China.
Junzhi YuDepartment of Gastroenterology, the Second Affiliated Hospital of Zhengzhou University, Zhengzhou, China.
Shiyang NingDepartment of Gastroenterology, the Second Affiliated Hospital of Zhengzhou University, Zhengzhou, China.
Baisui FengDepartment of Gastroenterology, the Second Affiliated Hospital of Zhengzhou University, Zhengzhou, China.
Yaohe WangCentre for Biomarkers and Biotherapeutics, Barts Cancer Institute, Queen Mary University of London, London, United Kingdom.
Na WangDepartment of Microbiology and Immunology, School of Basic Medical Sciences, Zhengzhou University, Zhengzhou, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Introduction: Lung cancer is the leading cause of cancer-related death worldwide, and its morbidity and mortality are increasing. Although low-dose CT lung cancer screening has been shown to reduce lung cancer mortality, its adoption rate is limited and the pace of its promotion is slow, highlighting the urgent need for more effective prevention measures. Prophylactic vaccines play a crucial role in cancer prevention. Our previous studies indicated that mice immunized with a prophylactic vaccine based on lung cancer cell lines KPL 160302S, derived from early-stage murine lung cancer tissues, exhibited a significantly extended survival period, with a strong anti-tumor immune response. While the vaccine based on KPL 160424S, derived from advanced-stage murine lung cancer tissues, failed to extend survival time and demonstrated limited capacity to stimulate anti-tumor immunity. Methods: To investigate the fundamental reason for the difference between KPL 160302S and KPL 160424S vaccines, we employed bioinformatics methods and immune related experiments to explore the effects and mechanisms of the screened neoantigens. Results: Our findings demonstrated that immunization with the Ddx21 mutant peptide (Ddx21MT), unique to KPL 160302S, could significantly increase the proportion of central memory T cells (TCM) in mice and activate anti-tumor immunity. Discussion: These results suggest that the Ddx21MT is a highly effective neoantigen that can activate anti-tumor immunity, which can serve as an important component in developing a lung cancer vaccine and is expected to be used in combination with other immunotherapy approaches.

Indexed as

Antigens, NeoplasmCancer VaccinesDEAD-box RNA HelicasesLung NeoplasmsPeptidesAnimalsCell Line, TumorFemaleHumansMiceMice, Inbred C57BLMutationAntigens, NeoplasmCancer VaccinesDEAD-box RNA HelicasesPeptidescentral memory T cellsDdx21lung cancerneoantigenprophylactic vaccine

Identifiers

PMID39981234
PMCPMC11839773

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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.