Evidence map›Paper›PMID 29282521›Full record

ArticleJournal of molecular medicine (Berlin, Germany)2018

Engineered exosomes emerging from muscle cells break immune tolerance to HER2 in transgenic mice and induce antigen-specific CTLs upon challenge by human dendritic cells.

Simona Anticoli, Eleonora Aricò, Claudia Arenaccio, Francesco Manfredi, Chiara Chiozzini, Eleonora Olivetta, Flavia Ferrantelli, Laura Lattanzi, Maria Teresa D'Urso, Enrico Proietti and 1 more

Abstract read
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In one paragraph

Article in Journal of molecular medicine (Berlin, Germany), 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed
1.2field-weighted citation impact, top 20% 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

22 citing papers in PubMed, 36 citations in OpenAlex.

  1. Article
  2. Review
  3. Review
  4. Article
  5. Review
  6. Article
  7. Engineered exosomes from different sources for cancer-targeted therapy.Signal transduction and targeted therapy · 2023
    Review
  8. Article
  9. Article
  10. Extracellular Vesicles and Their Use as Vehicles of Immunogens.Methods in molecular biology (Clifton, N.J.) · 2022
    Article
  11. Small extracellular vesicles in cancer.Bioactive materials · 2021
    Review
  12. Virus-Induced CD8Vaccines · 2021
    Article
  13. Article
  14. Article
  15. Simultaneous CD8Vaccines · 2021
    Article
  16. Article
  17. Article
  18. Article
  19. Review
  20. 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 at 1 institution in 1 country.

Simona AnticoliNational Center for Global Health, Istituto Superiore di Sanità (ISS), Viale Regina Elena 299, 00161, Rome, Italy.
Eleonora AricòFabioCell, Core Facilities, ISS, Viale Regina Elena 299, 00161, Rome, Italy.
Claudia ArenaccioNational Center for Global Health, Istituto Superiore di Sanità (ISS), Viale Regina Elena 299, 00161, Rome, Italy.
Francesco ManfrediNational Center for Global Health, Istituto Superiore di Sanità (ISS), Viale Regina Elena 299, 00161, Rome, Italy.
Chiara ChiozziniNational Center for Global Health, Istituto Superiore di Sanità (ISS), Viale Regina Elena 299, 00161, Rome, Italy.
Eleonora OlivettaNational Center for Global Health, Istituto Superiore di Sanità (ISS), Viale Regina Elena 299, 00161, Rome, Italy.
Flavia FerrantelliNational Center for Global Health, Istituto Superiore di Sanità (ISS), Viale Regina Elena 299, 00161, Rome, Italy.
Laura LattanziDepartment of Oncology and Molecular Medicine, ISS, Viale Regina Elena 299, 00161, Rome, Italy.
Maria Teresa D'UrsoNational Center for Animal Experimentation and Health, ISS, Viale Regina Elena 299, 00161, Rome, Italy.
Enrico ProiettiDepartment of Oncology and Molecular Medicine, ISS, Viale Regina Elena 299, 00161, Rome, Italy.
Maurizio FedericoNational Center for Global Health, Istituto Superiore di Sanità (ISS), Viale Regina Elena 299, 00161, Rome, Italy. maurizio.federico@iss.it.
Istituto Superiore di Sanità · IT

Funding

Ministero della Salute RF-2010-2308334
6 · The paper itself

Abstract

We recently described a novel biotechnological platform for the production of unrestricted cytotoxic T lymphocyte (CTL) vaccines. It relies on in vivo engineering of exosomes, i.e., nanovesicles constitutively released by all cells, with full-length antigens of choice upon fusion with an exosome-anchoring protein referred to as Nef KEY MESSAGES: We established a novel, exosome-based method to produce unrestricted CTL vaccines. This strategy is effective in breaking the tolerance towards tumor self-antigens. Our method is also useful to elicit antigen-specific CTL immunity in humans. These findings open the way towards the use of this antitumor strategy in clinic.

Indexed as

AnimalsCells, CulturedDendritic CellsErb-b2 Receptor Tyrosine KinasesExosomesHumansImmune ToleranceImmunotherapyMice, TransgenicMusclesNeoplasmsT-Lymphocytes, CytotoxicErb-b2 Receptor Tyrosine KinasesCTL vaccinesExosomesHER2/neuImmunological toleranceNef

Identifiers

PMID29282521
OpenAlexW2778428910

What OpenQuestion holds

Textmetadata
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.