Evidence map›Paper›PMID 42315874›Full record

ArticleNPJ vaccines2026

Development of a multi-epitope mRNA vaccine targeting tumor-associated antigens for esophageal squamous cell carcinoma.

Henghui Zhang, Hao Liang, Tingting Dai, Ning Shen, Chenlu Liu, Yang Zhou, Zhenhua Wei, Zhongqiu Wu, Pengfei Yu, Quan Zhang and 9 more

Abstract read
In one paragraph

Article in NPJ vaccines, 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
–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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

19 authors.

Henghui Zhang *Biomedical Innovation Center, Beijing Shijitan Hospital, Capital Medical University, Beijing, China. zhhbao@ccmu.edu.cn.
Hao Liang *Engineering Research Center of Immunocellular Therapy, Beijing, China.
Tingting Dai *Key Laboratory of Carcinogenesis and Translational Research (Ministry of Education/ Beijing), Department of Gastrointestinal Oncology, Peking University Cancer Hospital and Institute, Beijing, China.
Ning ShenEngineering Research Center of Immunocellular Therapy, Beijing, China.
Chenlu LiuEngineering Research Center of Immunocellular Therapy, Beijing, China.
Yang ZhouEngineering Research Center of Immunocellular Therapy, Beijing, China.
Zhenhua WeiEngineering Research Center of Immunocellular Therapy, Beijing, China.
Zhongqiu WuEngineering Research Center of Immunocellular Therapy, Beijing, China.
Pengfei YuEngineering Research Center of Immunocellular Therapy, Beijing, China.
Quan ZhangEngineering Research Center of Immunocellular Therapy, Beijing, China.
Xiaona ZhangEngineering Research Center of Immunocellular Therapy, Beijing, China.
Jinxuan YuEngineering Research Center of Immunocellular Therapy, Beijing, China.
Xuefeng JiEngineering Research Center of Immunocellular Therapy, Beijing, China.
Airong YangEngineering Research Center of Immunocellular Therapy, Beijing, China.
Cuiping AnEngineering Research Center of Immunocellular Therapy, Beijing, China.
Ying HanEngineering Research Center of Immunocellular Therapy, Beijing, China.
Xi JiaoKey Laboratory of Carcinogenesis and Translational Research (Ministry of Education/ Beijing), Department of Gastrointestinal Oncology, Peking University Cancer Hospital and Institute, Beijing, China.
Lu QianEngineering Research Center of Immunocellular Therapy, Beijing, China. qianlubj@163.com.
Zhihao LuKey Laboratory of Carcinogenesis and Translational Research (Ministry of Education/ Beijing), Department of Gastrointestinal Oncology, Peking University Cancer Hospital and Institute, Beijing, China. zhihaolupku@bjmu.edu.cn.

Funding

Beijing Hospitals Authority Clinical Medicine Development of special funding support ZLRK202326
6 · The paper itself

Abstract

Esophageal squamous cell carcinoma (ESCC) has limited treatment options post-immune checkpoint inhibitor (ICI) resistance. We developed IPM514, a universal multi-epitope mRNA lipid nanoparticle (LNP) vaccine targeting tumor-associated antigens identified via transcriptomic analysis of TCGA/GTEx datasets and validated in 132 ESCC patients. IPM514 contains 15 fragments from 9 antigens, covering most patients and over half of HLA subtypes. Peripheral blood mononuclear cells (PBMCs) from healthy donors and ESCC patients stimulated with IPM514 effectively expanded specific T cells that exhibited significant cytotoxic activity against ESCC and other squamous cell carcinomas with similar antigen profiles. In HLA-transgenic mouse models, IPM514 suppressed tumor growth, extended survival, and provided durable protection. Importantly, combination therapy with PD-1 blockade augmented antitumor efficacy by promoting immune cell infiltration, upregulating antigen presentation pathways, and reprogramming the tumor microenvironment toward an anti-tumorigenic state. These results demonstrate IPM514 represents a promising novel mRNA vaccine strategy for improving ESCC immunotherapy.

Identifiers

PMID42315874
PMCPMC13639008

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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.