Evidence map›Paper›PMID 31436946›Full record

ArticleACS nano2019

Rapid On-Demand Extracellular Vesicle Augmentation with Versatile Oligonucleotide Tethers.

Saigopalakrishna S Yerneni, Sushil Lathwal, Pradeep Shrestha, Haval Shirwan, Krzysztof Matyjaszewski, Lee Weiss, Esma S Yolcu, Phil G Campbell, Subha R Das

Abstract read
In one paragraph

Article in ACS nano, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 44 papers.

0numbers the graph read from it
0cells of the map it votes in
44citing 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

44 citing papers in PubMed.

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  17. Bioengineered nanotechnology for nucleic acid delivery.Journal of controlled release : official journal of the Controlled Release Society · 2023
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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

9 authors.

Saigopalakrishna S YerneniDepartment of Biomedical Engineering , Carnegie Mellon University , Pittsburgh , Pennsylvania 15213 , United States.
Sushil LathwalDepartment of Chemistry , Carnegie Mellon University , Pittsburgh , Pennsylvania 15213 , United States.
Pradeep ShresthaInstitute for Cellular Therapeutics and Department of Microbiology and Immunology , University of Louisville , Louisville , Kentucky 40292 , United States.
Haval ShirwanInstitute for Cellular Therapeutics and Department of Microbiology and Immunology , University of Louisville , Louisville , Kentucky 40292 , United States.
Krzysztof MatyjaszewskiDepartment of Chemistry , Carnegie Mellon University , Pittsburgh , Pennsylvania 15213 , United States.ORCID 0000-0003-1960-3402
Lee WeissDepartment of Biomedical Engineering , Carnegie Mellon University , Pittsburgh , Pennsylvania 15213 , United States.
Esma S YolcuInstitute for Cellular Therapeutics and Department of Microbiology and Immunology , University of Louisville , Louisville , Kentucky 40292 , United States.
Phil G CampbellDepartment of Biomedical Engineering , Carnegie Mellon University , Pittsburgh , Pennsylvania 15213 , United States.
Subha R DasDepartment of Chemistry , Carnegie Mellon University , Pittsburgh , Pennsylvania 15213 , United States.ORCID 0000-0002-5353-0422

Funding

Targeted delivery of immunomodulatory biologics for induction of immune privilege to allogeneic pancreatic islet graftsU01AI132817 · NIAID · UNIVERSITY OF MISSOURI-COLUMBIA · PI GARCIA, ANDRES J, SHIRWAN, HAVAL · 2017 to 2021
$2.0M
A novel immunomodulatory approach to overcome innate and adaptiveimmune barriers to islet transplantationR01AI121281 · NIAID · UNIVERSITY OF MISSOURI-COLUMBIA · PI SHIRWAN, HAVAL · 2019 to 2024
$1.9M
NIAID NIH HHS R01 AI121281NIAID NIH HHS U01 AI132817
6 · The paper itself

Abstract

Exosomes show potential as ideal vehicles for drug delivery because of their natural role in transferring biological cargo between cells. However, current methods to engineer exosomes without negatively impacting their function remain challenging. Manipulating exosome-secreting cells is complex and time-consuming, while direct functionalization of exosome surface proteins suffers from low specificity and low efficiency. We demonstrate a rapid, versatile, and scalable method with oligonucleotide tethers to enable diverse surface functionalization on both human and murine exosomes. These exosome surface modifiers, which range from reactive functional groups and small molecules to aptamers and large proteins, can readily and efficiently enhance native exosome properties. We show that cellular uptake of exosomes can be specifically altered with a tethered AS1411 aptamer, and targeting specificity can be altered with a tethered protein. We functionalize exosomes with an immunomodulatory protein, FasL, and demonstrate their biological activity both

Indexed as

AnimalsApoptosisAptamers, NucleotideBioprintingCell ProliferationClick ChemistryDNAExosomesExtracellular VesiclesFas Ligand ProteinHEK293 CellsHumansJurkat CellsMice, Inbred C57BLOligonucleotidesT-LymphocytesAptamers, NucleotideDNAFas Ligand ProteinOligonucleotidesaptamerDNAdrug deliveryexosomeextracellular vesicleimmunomodulationmembrane engineering

Identifiers

PMID31436946
PMCPMC6800810

What OpenQuestion holds

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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.