Evidence map›Paper›PMID 37525396›Full record

ArticleJournal of extracellular vesicles2023

T-cell derived extracellular vesicles prime macrophages for improved STING based cancer immunotherapy.

Aida S Hansen, Lea S Jensen, Kristine R Gammelgaard, Kristoffer G Ryttersgaard, Christian Krapp, Jesper Just, Kasper L Jønsson, Pia B Jensen, Thomas Boesen, Mogens Johansen and 3 more

Erratum issuedOpen access · goldAbstract read
In one paragraph

Article in Journal of extracellular vesicles, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed
4.8field-weighted citation impact, top 4% of its field
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

18 citing papers in PubMed, 31 citations in OpenAlex.

  1. Review
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  6. Mouse TThe Journal of allergy and clinical immunology · 2025
    Article
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  8. Article
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  12. TcEVdb: a database for T-cell-derived small extracellular vesicles from single-cell transcriptomes.Database : the journal of biological databases and curation · 2025
    Article
  13. Exosomes and solid cancer therapy: where are we now?Medical oncology (Northwood, London, England) · 2025
    Review
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

13 authors at 1 institution in 1 country.

Aida S HansenDepartment of Biomedicine, Aarhus University, Health, Aarhus Midtjylland, Denmark.
Lea S JensenDepartment of Biomedicine, Aarhus University, Health, Aarhus Midtjylland, Denmark.
Kristine R GammelgaardDepartment of Biomedicine, Aarhus University, Health, Aarhus Midtjylland, Denmark.
Kristoffer G RyttersgaardDepartment of Biomedicine, Aarhus University, Health, Aarhus Midtjylland, Denmark.
Christian KrappDepartment of Biomedicine, Aarhus University, Health, Aarhus Midtjylland, Denmark.
Jesper JustDepartment of Clinical Medicine, Center of Functionally Integrative Neuroscience, Aarhus University, Aarhus Midtjylland, Denmark.
Kasper L JønssonDepartment of Biomedicine, Aarhus University, Health, Aarhus Midtjylland, Denmark.
Pia B JensenInterdiciplinary Nanoscience Center - iNANO, Aarhus University, Aarhus Midtjylland, Denmark.
Thomas BoesenInterdiciplinary Nanoscience Center - iNANO, Aarhus University, Aarhus Midtjylland, Denmark.
Mogens JohansenDepartment of Forensic Medicine, Aarhus University, Aarhus Midtjylland, Denmark.
Anders EtzerodtDepartment of Biomedicine, Aarhus University, Health, Aarhus Midtjylland, Denmark.
Bent W DeleuranDepartment of Biomedicine, Aarhus University, Health, Aarhus Midtjylland, Denmark.
Martin R JakobsenDepartment of Biomedicine, Aarhus University, Health, Aarhus Midtjylland, Denmark.ORCID https://orcid.org/0000-0001-8847-9201
Aarhus University · DK

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

A key phenomenon in cancer is the establishment of a highly immunosuppressive tumour microenvironment (TME). Despite advances in immunotherapy, where the purpose is to induce tumour recognition and hence hereof tumour eradication, the majority of patients applicable for such treatment still fail to respond. It has been suggested that high immunological activity in the tumour is essential for achieving effective response to immunotherapy, which therefore have led to exploration of strategies that triggers inflammatory pathways. Here activation of the stimulator of interferon genes (STING) signalling pathway has been considered an attractive target, as it is a potent trigger of pro-inflammatory cytokines and types I and III interferons. However, immunotherapy combined with targeted STING agonists has not yielded sustained clinical remission in humans. This suggests a need for exploring novel adjuvants to improve the innate immunological efficacy. Here, we demonstrate that extracellular vesicles (EVs), derived from activated CD4

Indexed as

Extracellular VesiclesNeoplasmsHumansImmunotherapyInterferonsMacrophagesT-LymphocytesTumor MicroenvironmentInterferonscancer immunologyCDN therapyextracellular vesiclesIFNγmacrophagesSTINGT cells

Identifiers

PMID37525396
PMCPMC10390661
OpenAlexW4385442683

What OpenQuestion 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 OpenQuestion graph.