Evidence map›Paper›PMID 32748889›Full record

ArticleInternational journal of molecular sciences2020

Orally Administered Exosomes Suppress Mouse Delayed-Type Hypersensitivity by Delivering miRNA-150 to Antigen-Primed Macrophage APC Targeted by Exosome-Surface Anti-Peptide Antibody Light Chains.

Katarzyna Nazimek, Krzysztof Bryniarski, Wlodzimierz Ptak, Tom Groot Kormelink, Philip W Askenase

Open access · goldAbstract read
In one paragraph

Article in International journal of molecular sciences, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 24 papers.

0numbers the graph read from it
0cells of the map it votes in
24citing papers in PubMed
1.8field-weighted citation impact, top 14% 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

24 citing papers in PubMed, 32 citations in OpenAlex.

  1. Review
  2. Review
  3. Review
  4. mTOR Signaling in Macrophages: All Depends on the Context.International journal of molecular sciences · 2025
    Review
  5. Review
  6. Extracellular Vesicles for Disease Treatment.International journal of nanomedicine · 2025
    Review
  7. The OT-II model reveals dualFrontiers in immunology · 2025
    Article
  8. Macrophage Functions in Psoriasis: Lessons from Mouse Models.International journal of molecular sciences · 2024
    Review
  9. Article
  10. Review
  11. Review
  12. Review
  13. Review
  14. Functional Roles of Exosomes in Allergic Contact Dermatitis.Journal of microbiology and biotechnology · 2022
    Review
  15. Review
  16. Extracellular Vesicles-Oral Therapeutics of the Future.International journal of molecular sciences · 2022
    Review
  17. Review
  18. Review
  19. Article
  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

5 authors at 2 institutions in 2 countries.

Katarzyna NazimekDepartment of Immunology, Faculty of Medicine, Medical College, Jagiellonian University, 31-121 Krakow, Poland.ORCID 0000-0003-1302-117X
Krzysztof BryniarskiDepartment of Immunology, Faculty of Medicine, Medical College, Jagiellonian University, 31-121 Krakow, Poland.ORCID 0000-0001-8537-9176
Wlodzimierz PtakDepartment of Immunology, Faculty of Medicine, Medical College, Jagiellonian University, 31-121 Krakow, Poland.
Tom Groot KormelinkSection of Rheumatology, Allergy and Immunology, Department of Internal Medicine, School of Medicine, Yale University, New Haven, CT 06520-8013, USA.
Philip W AskenaseSection of Rheumatology, Allergy and Immunology, Department of Internal Medicine, School of Medicine, Yale University, New Haven, CT 06520-8013, USA.ORCID 0000-0001-8345-120X
Jagiellonian University · PLYale University · US

Funding

Ministerstwo Nauki i Szkolnictwa Wyższego 6354/IA/156/2013Narodowe Centrum Nauki 2013/11/B/NZ6/02041NIH HHS AI-07174NIH HHS AI-076366NIH HHS AI-1053786
6 · The paper itself

Abstract

We previously discovered suppressor T cell-derived, antigen (Ag)-specific exosomes inhibiting mouse hapten-induced contact sensitivity effector T cells by targeting antigen-presenting cells (APCs). These suppressive exosomes acted Ag-specifically due to a coating of antibody free light chains (FLC) from Ag-activated B1a cells. Current studies are aimed at determining if similar immune tolerance could be induced in cutaneous delayed-type hypersensitivity (DTH) to the protein Ag (ovalbumin, OVA). Intravenous administration of a high dose of OVA-coupled, syngeneic erythrocytes similarly induced CD3

Indexed as

AnimalsAntibodiesAntigen-Presenting CellsAntigensExosomesFemaleHypersensitivity, DelayedImmune ToleranceImmunoglobulin Light ChainsMacrophagesMice, Inbred BALB CMice, Inbred C57BLMice, Inbred CBAMice, KnockoutMicroRNAsOvalbuminAntibodiesAntigensImmunoglobulin Light ChainsMicroRNAsMirn150 microRNA, mouseOvalbuminantibody free light chains (FLC)delayed-type hypersensitivity (DTH)exosomesextracellular vesicles (EVs)miRNAmiRNA-150oral therapysuppressor T cells

Identifiers

PMID32748889
PMCPMC7432818
OpenAlexW3046435409

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.