Evidence map›Paper›PMID 32109144›Full record

ReviewAmerican journal of respiratory cell and molecular biology2020

Extracellular Vesicles: A New Frontier for Research in Acute Respiratory Distress Syndrome.

Rahul Y Mahida, Shotaro Matsumoto, Michael A Matthay

Open access · greenAbstract readReview
In one paragraph

Review in American journal of respiratory cell and molecular biology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 45 papers.

0numbers the graph read from it
0cells of the map it votes in
45citing papers in PubMed
4.1field-weighted citation impact, top 5% 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

45 citing papers in PubMed, 58 citations in OpenAlex.

  1. Review
  2. Review
  3. Article
  4. Review
  5. Rewiring the Lung-CNS Axis After Spinal Cord Injury.Journal of inflammation research · 2026
    Review
  6. Review
  7. Article
  8. Article
  9. Review
  10. Article
  11. Regenerative Signatures in BAL of Acute Respiratory Distress Syndrome.American journal of respiratory cell and molecular biology · 2024
    Article
  12. Article
  13. Article
  14. Myeloid Extracellular Vesicles: New Players in Indirect Lung Injury.American journal of respiratory cell and molecular biology · 2023
    Article
  15. Article
  16. Review
  17. Review
  18. 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

3 authors at 3 institutions in 3 countries.

Rahul Y MahidaCardiovascular Research Institute.ORCID 0000-0003-1100-8684
Shotaro MatsumotoCardiovascular Research Institute.
Michael A MatthayCardiovascular Research Institute.
Cardiovascular Institute Hospital · JPTokyo Medical and Dental University · JPUniversity of California, San Francisco · US

Funding

Precision Medicine in the Acute Respiratory Distress SyndromeR35HL140026 · NHLBI · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI CALFEE, CAROLYN · 2018 to 2024
$6.8M
NOVEL PARACRINE MECHANISMS FOR CELL-BASED THERAPY OF INJURED LUNGSR01HL134828 · NHLBI · UNIVERSITY OF TEXAS HLTH CTR AT TYLER · PI JI, HONG-LONG · 2017 to 2025
$3.4M
Albumin Nanoparticles Incorporating Piceatannol (PANPs) for ALI/ARDS therapyR42HL126456 · NHLBI · NANO BIOTHERAPEUTICS, INC. · PI KANTETI, PRASAD V. S., MALIK, ASRAR B. · 2017 to 2019
$2.7M
HLS13-13 Albumin nanoparticle based technology to treat ARDSR41HL126456 · NHLBI · CELL BIOLOGICS, INC. · PI BACHMAIER, KURT · 2015 to 2016
$688k
Medical Research Council MR/N021185/1NHLBI NIH HHS R01 HL134828NHLBI NIH HHS R35 HL140026NHLBI NIH HHS R41 HL126456NHLBI NIH HHS R42 HL126456
6 · The paper itself

Abstract

Recent research on extracellular vesicles (EVs) has provided new insights into pathogenesis and potential therapeutic options for acute respiratory distress syndrome (ARDS). EVs are membrane-bound anuclear structures that carry important intercellular communication mechanisms, allowing targeted transfer of diverse biologic cargo, including protein, mRNA, and microRNA, among several different cell types. In this review, we discuss the important role EVs play in both inducing and attenuating inflammatory lung injury in ARDS as well as in sepsis, the most important clinical cause of ARDS. We discuss the translational challenges that need to be overcome before EVs can also be used as prognostic biomarkers in patients with ARDS and sepsis. We also consider how EVs may provide a platform for novel therapeutics in ARDS.

Indexed as

AnimalsBiomarkersCell CommunicationExtracellular VesiclesHumansMicroRNAsRespiratory Distress SyndromeRNA, MessengerBiomarkersMicroRNAsRNA, Messengeracute lung injuryacute respiratory distress syndromeextracellular vesiclessepsis

Identifiers

PMID32109144
PMCPMC7328246
OpenAlexW3007923702

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.