Evidence map›Paper›PMID 31456107›Full record

ReviewJournal of neuroimmune pharmacology : the official journal of the Society on NeuroImmune Pharmacology2020

Strategies for the use of Extracellular Vesicles for the Delivery of Therapeutics.

Susmita Sil, Raghubendra Singh Dagur, Ke Liao, Eric S Peeples, Guoku Hu, Palsamy Periyasamy, Shilpa Buch

Open access · greenAbstract readReview
In one paragraph

Review in Journal of neuroimmune pharmacology : the official journal of the Society on NeuroImmune Pharmacology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 77 papers.

0numbers the graph read from it
0cells of the map it votes in
77citing papers in PubMed
3.9field-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

77 citing papers in PubMed, 104 citations in OpenAlex.

  1. Review
  2. Review
  3. Article
  4. Article
  5. Review
  6. Article
  7. Extracellular vesicle-based therapies for neurodegenerative diseases.NeuroImmune pharmacology and therapeutics · 2025
    Review
  8. Review
  9. Review
  10. Review
  11. Advances in constructing biocompatible nanocarriers.Drug delivery and translational research · 2025
    Review
  12. Review
  13. Article
  14. Review
  15. Article
  16. Review
  17. Review
  18. Review
  19. Review
  20. Article

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

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

7 authors at 1 institution in 1 country.

Susmita SilDepartment of Pharmacology and Experimental Neuroscience, University of Nebraska Medical Center, Omaha, NE, 68198-5880, USA.
Raghubendra Singh DagurDepartment of Pharmacology and Experimental Neuroscience, University of Nebraska Medical Center, Omaha, NE, 68198-5880, USA.
Ke LiaoDepartment of Pharmacology and Experimental Neuroscience, University of Nebraska Medical Center, Omaha, NE, 68198-5880, USA.
Eric S PeeplesDepartment of Pediatrics, University of Nebraska Medical Center, Omaha, NE, USA.
Guoku HuDepartment of Pharmacology and Experimental Neuroscience, University of Nebraska Medical Center, Omaha, NE, 68198-5880, USA. guoku.hu@unmc.edu.
Palsamy PeriyasamyDepartment of Pharmacology and Experimental Neuroscience, University of Nebraska Medical Center, Omaha, NE, 68198-5880, USA. palsamy.periyasamy@unmc.edu.
Shilpa BuchDepartment of Pharmacology and Experimental Neuroscience, University of Nebraska Medical Center, Omaha, NE, 68198-5880, USA. sbuch@unmc.edu.
University of Nebraska Medical Center · US

Funding

Therapeutics Core (Page 286)P30MH062261 · NIMH · UNIVERSITY OF NEBRASKA MEDICAL CENTER · PI BUCH, SHILPA J., FOX, HOWARD S · 2000 to 2021
$37.7M
The combinatorial effects of Opiates and the emerging promoter-variant strains of HIV-1 subtype C on HIV neuropathogensis and latencyR01DA041751 · NIDA · UNIVERSITY OF NEBRASKA MEDICAL CENTER · PI BUCH, SHILPA J., BYRAREDDY, SIDDAPPA N · 2016 to 2020
$3.9M
The brain as a SIV reservoir under suppressive cART potentiation by drugs of abuseR01DA043164 · NIDA · UNIVERSITY OF NEBRASKA MEDICAL CENTER · PI BUCH, SHILPA J., BYRAREDDY, SIDDAPPA N · 2016 to 2020
$3.8M
HIV Tat & Morphine induce mircroglial migration & activation via release of miR-9 & 138R01DA040397 · NIDA · UNIVERSITY OF NEBRASKA MEDICAL CENTER · PI BUCH, SHILPA J., FOX, HOWARD S · 2015 to 2019
$2.5M
HIV-1 mediated synaptodendritic injury and microglial activation: Role of extracellular vesicle miRNAsR01MH112848 · NIMH · UNIVERSITY OF NEBRASKA MEDICAL CENTER · PI BUCH, SHILPA J., HU, GUOKU · 2017 to 2021
$2.1M
HIV Tat & cocaine-mediated alterations in microglial migration & activation involve epigenetic reulation of miRNAsR01DA043138 · NIDA · UNIVERSITY OF NEBRASKA MEDICAL CENTER · PI BUCH, SHILPA J., GUO, MINGLEI · 2016 to 2020
$1.9M
Intranasal delivery of exosomes loaded with miRs -223 and -124 as a therapeutic strategy for HAND in cocaine usersR21DA046831 · NIDA · UNIVERSITY OF NEBRASKA MEDICAL CENTER · PI CHIVERO, ERNEST, GURUMURTHY, CHANNABASAVAIAH · 2018 to 2019
$419k
Exosome-mediated anti-microRNA delivery into the CNS: A Novel Threpautic for HAND in opiate usersR21DA042704 · NIDA · UNIVERSITY OF NEBRASKA MEDICAL CENTER · PI GUO, MINGLEI, HU, GUOKU · 2017 to 2018
$414k
Role of miR-124 in HIV-1 Tat & cocaine mediated microglial activationR03DA044087 · NIDA · UNIVERSITY OF NEBRASKA MEDICAL CENTER · PI PERIYASAMY, PALSAMY · 2017 to 2018
$152k
NIDA NIH HHS R01 DA040397NIDA NIH HHS R01 DA041751NIDA NIH HHS R01 DA043138NIDA NIH HHS R01 DA043164NIDA NIH HHS R03 DA044087NIDA NIH HHS R21 DA042704NIDA NIH HHS R21 DA046831NIH HHS DA044087NIMH NIH HHS P30 MH062261NIMH NIH HHS R01 MH112848
6 · The paper itself

Abstract

Extracellular vesicles (EVs) are nanosized, membrane-bound vesicles released from eukaryotic and prokaryotic cells that can transport cargo containing DNA, RNA, lipids and proteins, between cells as a means of intercellular communication. Although EVs were initially considered to be cellular debris deprived of any essential biological functions, emerging literature highlights the critical roles of EVs in the context of intercellular signaling, maintenance of tissue homeostasis, modulation of immune responses, inflammation, cancer progression, angiogenesis, and coagulation under both physiological and pathological states. Based on the ability of EVs to shuttle proteins, lipids, carbohydrates, mRNAs, long non-coding RNAs (lncRNAs), microRNAs, chromosomal DNA, and mitochondrial DNA into target cells, the presence and content of EVs in biofluids have been exploited for biomarker research in the context of diagnosis, prognosis and treatment strategies. Additionally, owing to the characteristics of EVs such as stability in circulation, biocompatibility as well as low immunogenicity and toxicity, these vesicles have become attractive systems for the delivery of therapeutics. More recently, EVs are increasingly being exploited as conduits for delivery of therapeutics for anticancer strategies, immunomodulation, targeted drug delivery, tissue regeneration, and vaccination. In this review, we highlight and discuss the multiple strategies that are employed for the use of EVs as delivery vehicles for therapeutic agents, including the potential advantages and challenges involved. Graphical abstract.

Indexed as

Drug Delivery SystemsAnimalsBioengineeringBiomarkersCell CommunicationDrug CarriersExtracellular VesiclesHumansImmunomodulationBiomarkersDrug CarriersBioengineeringEV administrationEV loadingExtracellular vesicleTherapeutic application

Identifiers

PMID31456107
PMCPMC7044028
OpenAlexW2970839635

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.