Evidence map›Paper›PMID 24700864›Full record

ArticleJournal of the American Society of Nephrology : JASN2014

Human urinary exosomes as innate immune effectors.

Thomas F Hiemstra, Philip D Charles, Tannia Gracia, Svenja S Hester, Laurent Gatto, Rafia Al-Lamki, R Andres Floto, Ya Su, Jeremy N Skepper, Kathryn S Lilley and 1 more

Open access · bronzeAbstract read
In one paragraph

Article in Journal of the American Society of Nephrology : JASN, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 95 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
95citing papers in PubMed, 1 pooled it
6.0field-weighted citation impact, top 3% 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

95 citing papers in PubMed, 1 synthesis or guideline pooled it, 167 citations in OpenAlex.

  1. Guideline
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  5. Milk-Derived Extracellular Vesicles InhibitAnimals : an open access journal from MDPI · 2026
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  19. A thermo-resistant and RNase-sensitive cargo fromJournal of extracellular biology · 2023
    Article
  20. Article

35 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

11 authors at 6 institutions in 4 countries.

Thomas F HiemstraDepartment of Medicine, Cambridge Centre for Proteome Research and Cambridge Systems Biology Centre, Department of Biochemistry.
Philip D CharlesCambridge Centre for Proteome Research and Cambridge Systems Biology Centre, Department of Biochemistry.
Tannia GraciaDepartment of Medical Genetics, and.
Svenja S HesterSir William Dunn School of Pathology, University of Oxford, Oxford, United Kingdom.
Laurent GattoCambridge Centre for Proteome Research and Cambridge Systems Biology Centre, Department of Biochemistry.
Rafia Al-LamkiDepartment of Medicine.
R Andres FlotoDepartment of Medicine.
Ya SuDepartment of Medical Genetics, and.
Jeremy N SkepperMulti-Imaging Centre, Department of Anatomy, University of Cambridge, Cambridge, United Kingdom; and.
Kathryn S LilleyCambridge Centre for Proteome Research and Cambridge Systems Biology Centre, Department of Biochemistry, ksl23@cam.ac.uk fek1000@cam.ac.uk.
Fiona E Karet FranklDepartment of Medical Genetics, and ksl23@cam.ac.uk fek1000@cam.ac.uk.
Czech Academy of Sciences, Biology Centre · CZMedical Genetics Center · DEUniversity of Cambridge · GBCambridge School · PTProteome Sciences (United Kingdom) · GBUniversity of Oxford · GB

Funding

Medical Research CouncilWellcome Trust 088489Wellcome Trust 100140
6 · The paper itself

Abstract

Exosomes are small extracellular vesicles, approximately 50 nm in diameter, derived from the endocytic pathway and released by a variety of cell types. Recent data indicate a spectrum of exosomal functions, including RNA transfer, antigen presentation, modulation of apoptosis, and shedding of obsolete protein. Exosomes derived from all nephron segments are also present in human urine, where their function is unknown. Although one report suggested in vitro uptake of exosomes by renal cortical collecting duct cells, most studies of human urinary exosomes have focused on biomarker discovery rather than exosome function. Here, we report results from in-depth proteomic analyses and EM showing that normal human urinary exosomes are significantly enriched for innate immune proteins that include antimicrobial proteins and peptides and bacterial and viral receptors. Urinary exosomes, but not the prevalent soluble urinary protein uromodulin (Tamm-Horsfall protein), potently inhibited growth of pathogenic and commensal Escherichia coli and induced bacterial lysis. Bacterial killing depended on exosome structural integrity and occurred optimally at the acidic pH typical of urine from omnivorous humans. Thus, exosomes are innate immune effectors that contribute to host defense within the urinary tract.

Indexed as

Immunity, InnateAdultBiomarkersExosomesFemaleHumansMaleMicroscopy, ImmunoelectronProteomeUrinary TractUropathogenic Escherichia coliYoung AdultBiomarkersProteome

Identifiers

PMID24700864
PMCPMC4147985
OpenAlexW2131840270

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.