Evidence map›Paper›PMID 25847910›Full record

ArticleCytometry. Part A : the journal of the International Society for Analytical Cytology2015

Techniques to improve detection and analysis of extracellular vesicles using flow cytometry.

Heather C Inglis, Ali Danesh, Avani Shah, Jacques Lacroix, Philip C Spinella, Philip J Norris

Abstract read
In one paragraph

Article in Cytometry. Part A : the journal of the International Society for Analytical Cytology, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 47 papers.

0numbers the graph read from it
0cells of the map it votes in
47citing 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

47 citing papers in PubMed.

  1. Trial
  2. Article
  3. Review
  4. 80 years of extracellular vesicles: from discovery to clinical translation.Extracellular vesicles and circulating nucleic acids · 2026
    Review
  5. Article
  6. Article
  7. Article
  8. Review
  9. Article
  10. Article
  11. Article
  12. Article
  13. Article
  14. [Current Status and Prospects of Liquid Biopsy for Hepatocellular Carcinoma].The Korean journal of gastroenterology = Taehan Sohwagi Hakhoe chi · 2023
    Review
  15. Article
  16. Article
  17. Isolation and characterization of extracellular vesicles and future directions in diagnosis and therapy.Wiley interdisciplinary reviews. Nanomedicine and nanobiotechnology · 2023
    Review
  18. Extracellular Vesicles as Biomarkers in Liver Disease.International journal of molecular sciences · 2022
    Review
  19. Article
  20. Article
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

6 authors.

Heather C InglisBlood Systems Research Institute, San Francisco, California.
Ali DaneshBlood Systems Research Institute, San Francisco, California.
Avani ShahBlood Systems Research Institute, San Francisco, California.
Jacques LacroixDivision of Critical Care, Department of Pediatrics, University of Montreal, Quebec, Canada.
Philip C SpinellaDivision of Critical Care, Department of Pediatrics, Washington University School of Medicine, St. Louis, Missouri.
Philip J NorrisBlood Systems Research Institute, San Francisco, California.

Funding

Transfusion Medicine/Hemostasis Research Network: DCCU01HL072268 · NHLBI · NEW ENGLAND RESEARCH INSTITUTES, INC. · PI ASSMANN, SUSAN FERA · 2002 to 2012
$33.2M
Properties of stored RBCs: minimization of immune and vascular reactivityR01HL095470 · NHLBI · VITALANT · PI NORRIS, PHILIP J. · 2009 to 2012
$2.3M
NHLBI NIH HHS HL095470NHLBI NIH HHS R01 HL095470NHLBI NIH HHS U01 HL072268
6 · The paper itself

Abstract

Extracellular vesicles (EVs) range in size from 50 nm to 1 µm. Flow cytometry (FCM) is the most commonly used method for analyzing EVs; however, accurate characterization of EVs remains challenging due to their small size and lack of discrete positive populations. Here we report the use of optimization techniques that are especially well-suited for analyzing EVs from a high volume of clinical samples. Utilizing a two pronged approach that included 1) pre-filtration of antibodies to remove aggregates, followed by 2) detergent lysis of a replicate sample to account for remaining false positive events, we were able to effectively limit false positive non-EV events. In addition, we show that lysed samples are a useful alternative to isotypes for setting gates to exclude background fluorescence. To reduce background, we developed an approach using filters to "wash" samples post-staining thus providing a faster alternative to ultracentrifugation and sucrose gradient fractionation. In conclusion, use of these optimized techniques enhances the accuracy and efficiency of EV detection using FCM.

Indexed as

Extracellular VesiclesFlow CytometryAntibodiesAntigens, CDFiltrationHumansStaining and LabelingAntibodiesAntigens, CDantibody aggregatesextracellular vesiclesfiltrationflow cytometrymicroparticles

Identifiers

PMID25847910
PMCPMC4876854

What OpenQuestion holds

Textmetadata
LicenceTDM
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.