Evidence map›Paper›PMID 41872203›Full record

ArticleNature communications2026

Spatiotemporally engineered tumor-derived extracellular vesicle-based scaffold vaccine for personalized cancer immunotherapy.

Qi Chen, Chenwei Jiang, Xinxing Du, Minglu Tang, Qi Shang, Cong Hu, Zehong Peng, Wei Xue, Liang Dong, Feihu Wang and 1 more

Abstract read
In one paragraph

Article in Nature communications, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Review
  2. 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

11 authors.

Qi Chen *Department of Urology, Renji Hospital, Shanghai Jiao Tong University School of Medicine, Shanghai, China.ORCID http://orcid.org/0009-0009-4286-0029
Chenwei Jiang *School of Biomedical Engineering, Shanghai Jiao Tong University, Shanghai, China.
Xinxing DuDepartment of Urology, Renji Hospital, Shanghai Jiao Tong University School of Medicine, Shanghai, China.ORCID http://orcid.org/0009-0001-3437-0021
Minglu TangSchool of Biomedical Engineering, Shanghai Jiao Tong University, Shanghai, China.
Qi ShangSchool of Biomedical Engineering, Shanghai Jiao Tong University, Shanghai, China.
Cong HuDepartment of Urology, Renji Hospital, Shanghai Jiao Tong University School of Medicine, Shanghai, China.
Zehong PengDepartment of Urology, Renji Hospital, Shanghai Jiao Tong University School of Medicine, Shanghai, China.
Wei XueDepartment of Urology, Renji Hospital, Shanghai Jiao Tong University School of Medicine, Shanghai, China. uroxuewei@163.com.ORCID http://orcid.org/0000-0001-9298-9941
Liang DongDepartment of Urology, Renji Hospital, Shanghai Jiao Tong University School of Medicine, Shanghai, China. drdongliang@126.com.
Feihu WangSchool of Biomedical Engineering, Shanghai Jiao Tong University, Shanghai, China. fhwang21@sjtu.edu.cn.ORCID http://orcid.org/0000-0002-0358-967X
Jiahua PanDepartment of Urology, Renji Hospital, Shanghai Jiao Tong University School of Medicine, Shanghai, China. panjiahua@renji.com.ORCID http://orcid.org/0009-0000-2126-7335

Funding

National Natural Science Foundation of China (National Science Foundation of China) 82227801National Natural Science Foundation of China (National Science Foundation of China) 82373358National Natural Science Foundation of China (National Science Foundation of China) 82472142National Natural Science Foundation of China (National Science Foundation of China) 82473851
6 · The paper itself

Abstract

Personalized vaccines demonstrate remarkable potential in leveraging tumor-specific adaptive immunity for cancer therapy. Nevertheless, current platforms face persistent challenges, including premature systemic clearance and imprecise antigen-presenting cell targeting, culminating in transient and inefficient antitumor immunity. Furthermore, the technical complexity, extended timelines, and prohibitive costs required for tumor-specific neoantigen identification continue to impede the clinical translation of personalized cancer vaccines. Here, we report a tumor-derived extracellular vesicle-based scaffold vaccine that elicits robust and durable antitumor immunity for personalized cancer immunotherapy. Following subcutaneous administration, the in situ-formed hydrogel vaccine serves as a sustained reservoir for tumor-derived extracellular vesicle antigens and adjuvants while recruiting antigen-presenting dendritic cells to accumulate within the scaffold. Upon exposure to this antigen-rich depot, immature dendritic cells undergo efficient activation, with subsequently matured dendritic cells migrating to draining lymph nodes, where they induce potent and persistent tumor-specific CD8

Indexed as

Cancer VaccinesExtracellular VesiclesImmunotherapyNeoplasmsAnimalsAntigens, NeoplasmCD8-Positive T-LymphocytesCell Line, TumorDendritic CellsFemaleHumansHydrogelsMiceMice, Inbred C57BLPrecision MedicineAntigens, NeoplasmCancer VaccinesHydrogels

Identifiers

PMID41872203
PMCPMC13171897

What Socratic holds

Textmetadata
LicenceCC BY-NC-ND
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 Socratic graph.