Evidence map›Paper›PMID 34423113›Full record

ArticleAdvanced therapeutics2021

Therapeutic Potential of Extracellular Vesicles for Sepsis Treatment.

Stephanie M Kronstadt, Alex E Pottash, Daniel Levy, Sheng Wang, Wei Chao, Steven M Jay

Open access · greenAbstract read
In one paragraph

Article in Advanced therapeutics, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed
1.5field-weighted citation impact, top 18% 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

18 citing papers in PubMed, 26 citations in OpenAlex.

  1. Article
  2. Review
  3. Extracellular vesicles decoying across host immunity.Journal of leukocyte biology · 2025
    Review
  4. Review
  5. Article
  6. Article
  7. Review
  8. Review
  9. Review
  10. The multifaceted role of aquaporins in physiological cell migration.American journal of physiology. Cell physiology · 2023
    Review
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  12. Review
  13. Review
  14. Article
  15. Article
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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 at 2 institutions in 1 country.

Stephanie M KronstadtFischell Department of Bioengineering, University of Maryland, 3102 A. James Clark Hall, College Park, MD 20742, USA.
Alex E PottashFischell Department of Bioengineering, University of Maryland, 3102 A. James Clark Hall, College Park, MD 20742, USA.
Daniel LevyFischell Department of Bioengineering, University of Maryland, 3102 A. James Clark Hall, College Park, MD 20742, USA.
Sheng WangTranslational Research Program, Department of Anesthesiology and Center for Shock Trauma and Anesthesiology Research, University of Maryland School of Medicine, Baltimore, MD 21201, USA.
Wei ChaoTranslational Research Program, Department of Anesthesiology and Center for Shock Trauma and Anesthesiology Research, University of Maryland School of Medicine, Baltimore, MD 21201, USA.
Steven M JayFischell Department of Bioengineering and Program in Molecular and, Cell Biology, University of Maryland, 3102 A. James Clark Hall, College Park, MD 20742, USA.
University of Maryland, College Park · USUniversity of Maryland, Baltimore · US

Funding

Characterization of the Cardiac Progenitor Cell Exosomes for Optimal TherapeuticsR01HL141922 · NHLBI · UNIVERSITY OF MARYLAND BALTIMORE · PI KAUSHAL, SUNJAY · 2019 to 2022
$2.8M
Dementia Following Spinal Cord Injury: Mechanism and Therapeutic TargetingRF1NS110637 · NINDS · UNIVERSITY OF MARYLAND BALTIMORE · PI JAY, STEVEN MICHAEL, WU, JUNFANG · 2019 to 2019
$2.8M
Targeting brain inflammation and neurocognitive dysfunction in sepsisR01NS110567 · NINDS · UNIVERSITY OF MARYLAND BALTIMORE · PI CHAO, WEI, WU, JUNFANG · 2019 to 2024
$2.5M
Extracellular miRNAs, innate immunity, and critical illnessR35GM140822 · NIGMS · UNIVERSITY OF MARYLAND BALTIMORE · PI WEI CHAO · 2021 to 2026
$2.5M
Training in Host-pathogens interactionsT32AI089621 · NIAID · UNIV OF MARYLAND, COLLEGE PARK · PI LEE, VINCENT T, MCIVER, KEVIN S. · 2010 to 2025
$2.1M
Controlling Exosome Noncoding RNA Cargo for Enhanced Wound HealingR01HL141611 · NHLBI · UNIV OF MARYLAND, COLLEGE PARK · PI JAY, STEVEN MICHAEL · 2018 to 2022
$1.9M
Enabling exosome biomarker development via digitized single vesicle analysisR01GM130923 · NIGMS · UNIV OF MARYLAND, COLLEGE PARK · PI DEVOE, DON L, WHITE, IAN M · 2019 to 2022
$1.7M
Role of Extracellular MicroRNAs in Myocardial Ischemia-Reperfusion InjuryR01GM117233 · NIGMS · UNIVERSITY OF MARYLAND BALTIMORE · PI CHAO, WEI · 2016 to 2020
$1.6M
Extracellular miRNA-TLR7 Signaling in Sepsis PathogenesisR01GM122908 · NIGMS · UNIVERSITY OF MARYLAND BALTIMORE · PI CHAO, WEI · 2018 to 2019
$618k
NHLBI NIH HHS R01 HL141611NHLBI NIH HHS R01 HL141922NIAID NIH HHS T32 AI089621NIGMS NIH HHS R01 GM117233NIGMS NIH HHS R01 GM122908NIGMS NIH HHS R01 GM130923NIGMS NIH HHS R35 GM140822NINDS NIH HHS R01 NS110567NINDS NIH HHS RF1 NS110637
6 · The paper itself

Abstract

Sepsis is a deadly condition lacking a specific treatment despite decades of research. This has prompted the exploration of new approaches, with extracellular vesicles (EVs) emerging as a focal area. EVs are nanosized, cell-derived particles that transport bioactive components (i.e., proteins, DNA, and RNA) between cells, enabling both normal physiological functions and disease progression depending on context. In particular, EVs have been identified as critical mediators of sepsis pathophysiology. However, EVs are also thought to constitute the biologically active component of cell-based therapies and have demonstrated anti-inflammatory, anti-apoptotic, and immunomodulatory effects in sepsis models. The dual nature of EVs in sepsis is explored here, discussing their endogenous roles and highlighting their therapeutic properties and potential. Related to the latter component, prior studies involving EVs from mesenchymal stem/stromal cells (MSCs) and other sources are discussed and emerging producer cells that could play important roles in future EV-based sepsis therapies are identified. Further, how methodologies could impact therapeutic development toward sepsis treatment to enhance and control EV potency is described.

Indexed as

cell primingcell therapyexosomesmesenchymal stem/stromal cellsstem cells

Identifiers

PMID34423113
PMCPMC8378673
OpenAlexW3157427172

What OpenQuestion holds

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LicenceTDM
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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.