Evidence map›Paper›PMID 42209448›Full record

ArticleJournal of extracellular vesicles2026

Metabolic Tagging of Tumour Extracellular Vesicles for Targeted Modulation of Dendritic Cells.

Rimsha Bhatta, Wenhao Xu, Ruike Dai, Yusheng Liu, Jiadiao Zhou, Yixin Xue, Hua Wang

Abstract read
In one paragraph

Article in Journal of extracellular vesicles, 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

7 authors.

Rimsha BhattaDepartment of Materials Science and Engineering, University of Illinois at Urbana-Champaign, Urbana, Illinois, USA.
Wenhao XuDepartment of Materials Science and Engineering, University of Illinois at Urbana-Champaign, Urbana, Illinois, USA.
Ruike DaiDepartment of Materials Science and Engineering, University of Illinois at Urbana-Champaign, Urbana, Illinois, USA.
Yusheng LiuDepartment of Materials Science and Engineering, University of Illinois at Urbana-Champaign, Urbana, Illinois, USA.
Jiadiao ZhouDepartment of Materials Science and Engineering, University of Illinois at Urbana-Champaign, Urbana, Illinois, USA.
Yixin XueDepartment of Materials Science and Engineering, University of Illinois at Urbana-Champaign, Urbana, Illinois, USA.
Hua WangDepartment of Materials Science and Engineering, University of Illinois at Urbana-Champaign, Urbana, Illinois, USA.ORCID https://orcid.org/0000-0002-1157-8786

Funding

Biomaterials for Targeted Modulation of Conventional Type 1 Dendritic CellsR01CA274738 · NCI · UNIVERSITY OF ILLINOIS AT URBANA-CHAMPAIGN · PI WANG, HUA · 2022 to 2025
$2.2M
Metabolic tagging of tumor exosomes for developing enhanced exosome vaccinesR21CA270872 · NCI · UNIVERSITY OF ILLINOIS AT URBANA-CHAMPAIGN · PI WANG, HUA · 2023 to 2024
$364k
American Cancer SocietyDistinguished Scientise Award from Sontag FoundationNCI NIH HHS R01 CA274738NCI NIH HHS R01CA274738NCI NIH HHS R21 CA270872NCI NIH HHS R21CA270872NSF DMR 21-43673
6 · The paper itself

Abstract

Extracellular vesicles (EVs) have emerged as a promising alternative to cell-based therapies due to their benign safety profiles and favourable pharmacokinetic properties. Tumour EVs, in particular, have shown promise to function as a therapeutic cancer vaccine for various cancer types. However, the efficient and targeted delivery of EVs to dendritic cells, the prominent type of antigen-presenting cells in the body, remains a challenge. Here we report the metabolic tagging of tumour EVs with azido groups for subsequent conjugation of anti-DEC205 via efficient click chemistry. We showed that azido-sugars can metabolically label cancer cells with azido groups and that azido-labelled cells can secrete azido-tagged EVs. Anti-DEC205, upon facile modification with dibenzocyclooctyne, was successfully conjugated onto azido-tagged EVs. Anti-DEC205-conjugated EVs were preferentially internalized by dendritic cells over other types of immune cells, and improved the processing and presentation of EV-encased antigens by dendritic cells. We further demonstrated the ability of anti-DEC205-conjugated EVs to induce enhanced cytotoxic T lymphocyte responses and antitumor efficacy in comparison with control EVs. Our study provides a facile and universal approach to chemically tagging EVs and conjugating targeting moieties to EVs, for targeted modulation of cells of interest.

Indexed as

Dendritic CellsExtracellular VesiclesNeoplasmsAnimalsAntigens, CDAzidesCancer VaccinesCell Line, TumorClick ChemistryHumansLectins, C-TypeMiceMinor Histocompatibility AntigensReceptors, Cell SurfaceAntigens, CDAzidesCancer VaccinesDEC-205 receptorLectins, C-TypeMinor Histocompatibility AntigensReceptors, Cell Surfacecancer immunotherapycell targetingDEC205dendritic cellsmetabolic labelling

Identifiers

PMID42209448
PMCPMC13239806

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Registered trials

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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.