Evidence map›Paper›PMID 42188765›Full record

ArticleVaccines2026

Needle-Free Injection Enhances the Immunogenicity and Antitumor Efficacy of Whole-Cell Tumor Vaccines.

Chin-Yang Chang, Yu-Diao Kuan, Jiayu A Tai, Nan Ju, Yen-Liang Li, Munehisa Shimamura

Abstract read
In one paragraph

Article in 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

6 authors.

Chin-Yang ChangDepartment of Gene and Stem Cell Regenerative Therapeutics, Graduate School of Medicine, Osaka University, Osaka 565-0871, Japan.ORCID 0000-0002-7370-6026
Yu-Diao KuanDepartment of Device Application for Molecular Therapeutics, Graduate School of Medicine, Osaka University, Osaka 565-0871, Japan.ORCID 0000-0002-6591-4706
Jiayu A TaiDepartment of Device Application for Molecular Therapeutics, Graduate School of Medicine, Osaka University, Osaka 565-0871, Japan.
Nan JuDepartment of Gene and Stem Cell Regenerative Therapeutics, Graduate School of Medicine, Osaka University, Osaka 565-0871, Japan.ORCID 0000-0003-3421-7104
Yen-Liang LiNational Institute of Cancer Research, National Health Research Institutes, Tainan 704, Taiwan.
Munehisa ShimamuraDepartment of Gene and Stem Cell Regenerative Therapeutics, Graduate School of Medicine, Osaka University, Osaka 565-0871, Japan.ORCID 0000-0003-0374-0787

Funding

Japan Society for the Promotion of Science JP23K14648
6 · The paper itself

Abstract

BACKGROUND/

objectivesWhole-cell vaccines have demonstrated clinical potential in cancer treatment and recurrence prevention, yet their immunogenicity and dendritic cell (DC) activation remain suboptimal. This study aimed to evaluate whether a needle-free injector (NFI) could enhance the immunogenicity and antitumor efficacy of whole-cell tumor vaccines.

methodsAdaptive immune responses induced by NFI and traditional syringe injection (SYI) were compared following whole-cell vaccine administration. The morphology of vaccine fluid ejected by NFI and SYI was examined, and the effects on DC antigen uptake and activation were assessed. Antitumor efficacy was further evaluated in MC38 colon adenocarcinoma challenge models.

resultsNFI administration elicited stronger antigen-specific adaptive immune responses than SYI. The high-velocity pressure generated by NFI resulted in fragmentation of whole-cell vaccine material, and this morphological alteration was associated with enhanced DC antigen uptake and activation. These immunological improvements corresponded with superior tumor suppression in MC38 models following NFI-delivered vaccination.

conclusionsNFI delivery enhances the immunogenicity and antitumor efficacy of whole-cell tumor vaccines. These findings suggest that needle-free injectors may serve as a simple and effective strategy to improve the performance of whole-cell cancer vaccines.

Indexed as

antitumor immunitycancer immunotherapycancer vaccineneedle-free injectionwhole-cell tumor vaccine

Identifiers

PMID42188765
PMCPMC13211413

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

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.