Evidence map›Paper›PMID 40154979›Full record

ArticleJournal of extracellular vesicles2025

Direct delivery of immune modulators to tumour-infiltrating lymphocytes using engineered extracellular vesicles.

Xiabing Lyu, Tomoyoshi Yamano, Kanto Nagamori, Shota Imai, Toan Van Le, Dilireba Bolidong, Makie Ueda, Shota Warashina, Hidefumi Mukai, Seigo Hayashi and 3 more

Abstract read
In one paragraph

Article in Journal of extracellular vesicles, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing 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

10 citing papers in PubMed.

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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

13 authors.

Xiabing LyuWPI Nano Life Science Institute (NanoLSI), Kanazawa University, Kanazawa, Japan.
Tomoyoshi YamanoWPI Nano Life Science Institute (NanoLSI), Kanazawa University, Kanazawa, Japan.
Kanto NagamoriDepartment of Immunology, Graduate School of Medicine, Kanazawa University, Kanazawa, Japan.
Shota ImaiDepartment of Immunology, Graduate School of Medicine, Kanazawa University, Kanazawa, Japan.
Toan Van LeDepartment of Immunology, Graduate School of Medicine, Kanazawa University, Kanazawa, Japan.
Dilireba BolidongWPI Nano Life Science Institute (NanoLSI), Kanazawa University, Kanazawa, Japan.
Makie UedaDepartment of Immunology, Graduate School of Medicine, Kanazawa University, Kanazawa, Japan.
Shota WarashinaLaboratory for Molecular Delivery and Imaging Technology, RIKEN Center for Biosystems Dynamics Research, Kobe, Japan.
Hidefumi MukaiLaboratory for Molecular Delivery and Imaging Technology, RIKEN Center for Biosystems Dynamics Research, Kobe, Japan.
Seigo HayashiBiological Research Laboratories, Nissan Chemical Corporation, Saitama, Japan.
Kazutaka MatobaBiological Research Laboratories, Nissan Chemical Corporation, Saitama, Japan.
Taito NishinoBiological Research Laboratories, Nissan Chemical Corporation, Saitama, Japan.
Rikinari HanayamaWPI Nano Life Science Institute (NanoLSI), Kanazawa University, Kanazawa, Japan.ORCID https://orcid.org/0000-0003-2102-3386

Funding

Japan Agency for Medical Research and Development 22am0401019h0004Japan Agency for Medical Research and Development JP23ak0101178Japan Science and Technology Corporation JPMJCR18H4Japan Science and Technology Corporation JPMJFR2115Japan Science and Technology Corporation JPMJPR19HA
6 · The paper itself

Abstract

Extracellular vesicles (EVs) are important mediators of cell-cell communication, including immune regulation. Despite the recent development of several EV-based cancer immunotherapies, their clinical efficacy remains limited. Here, we created antigen-presenting EVs to express peptide-major histocompatibility complex (pMHC) class I, costimulatory molecule and IL-2. This enabled the selective delivery of multiple immune modulators to antigen-specific CD8

Indexed as

Extracellular VesiclesImmunologic FactorsLymphocytes, Tumor-InfiltratingAnimalsCD8-Positive T-LymphocytesCell Line, TumorHumansImmunotherapyMiceMice, Inbred C57BLNeoplasmsTumor MicroenvironmentImmunologic Factorsantigen presentationcancer immunotherapydrug deliveryextracellular vesicletargeted cytokine delivery

Identifiers

PMID40154979
PMCPMC11952836

What Socratic holds

Textmetadata
LicenceCC BY-NC
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.