Evidence map›Paper›PMID 40629076›Full record

ReviewCellular & molecular immunology2025

Eliciting antitumor immunity via therapeutic cancer vaccines.

Kun Peng, Xiaoxue Zhao, Yang-Xin Fu, Yong Liang

Abstract readReview
In one paragraph

Review in Cellular & molecular immunology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 51 papers, 3 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
51citing papers in PubMed, 3 pooled it
–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

51 citing papers in PubMed, 3 syntheses or guidelines pooled it.

  1. Pooled it
  2. Pooled it
  3. Pooled it
  4. New approach methodologies (NAMs) for preclinical and translational evaluation of mRNA-lipid nanoparticle (LNP) therapeutics.Journal of controlled release : official journal of the Controlled Release Society · 2026
    Review
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  10. Degraded sulfated galactan derived fromMolecular medicine reports · 2026
    Article
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  12. Universal off-the-shelf TGF-Acta pharmaceutica Sinica. B · 2026
    Article
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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

4 authors.

Kun Peng *Center for Cancer Biology, School of Basic Medical Sciences, Tsinghua University, Beijing, China.
Xiaoxue Zhao *Center for Cancer Biology, School of Basic Medical Sciences, Tsinghua University, Beijing, China.
Yang-Xin FuCenter for Cancer Biology, School of Basic Medical Sciences, Tsinghua University, Beijing, China. yangxinfu@mail.tsinghua.edu.cn.ORCID 0000-0001-8441-6617
Yong LiangCenter for Cancer Biology, School of Basic Medical Sciences, Tsinghua University, Beijing, China. yongliang@mail.tsinghua.edu.cn.

Funding

National Natural Science Foundation of China (National Science Foundation of China) 82250710684
6 · The paper itself

Abstract

Therapeutic cancer vaccines aim to expand and activate antigen-specific T cells for the targeted elimination of cancer cells. While early clinical trials faced challenges due to suboptimal antigen-specific T-cell activation, recent advancements in antigen discovery and vaccine platform engineering have revitalized the field. This review provides a comprehensive overview of key tumor antigens, including tumor-associated antigens, viral oncoprotein antigens, neoantigens, and cryptic antigens, with a focus on their immunogenicity and therapeutic potential. Advances in our understanding of traditional cancer vaccination targets, in conjunction with the timely identification of novel antigen epitopes, have facilitated the strategic selection of vaccination targets. We also discuss the evolution of cancer vaccine platforms-spanning peptide-based formulations to advanced mRNA vectors-emphasizing innovative strategies to optimize antigen delivery efficiency and adjuvant effects. Efficient antigen delivery and adjuvant selection overcome immune tolerance and tumor-induced immunosuppression. Furthermore, we examine recent clinical trial data and emerging combination approaches that integrate cancer vaccines with other immunotherapies to increase efficacy. While significant progress has been made, challenges remain in improving vaccine-induced T-cell responses, overcoming immune suppression, and translating these advances into effective clinical interventions. Addressing these hurdles will be critical for realizing the full potential of cancer vaccines in immunotherapy.

Indexed as

Cancer VaccinesNeoplasmsAnimalsAntigens, NeoplasmHumansImmunotherapyT-LymphocytesAntigens, NeoplasmCancer VaccinesCancer immunotherapyNeoantigenTumor-associated antigenVaccine

Identifiers

PMID40629076
PMCPMC12311208

What OpenQuestion holds

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LicenceCC BY
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Registered trials

None linked

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.