Evidence map›Paper›PMID 36298724›Full record

ArticleViruses2022

A Novel Piggyback Strategy for mRNA Delivery Exploiting Adenovirus Entry Biology.

Myungeun Lee, Paul J Rice-Boucher, Logan Thrasher Collins, Ernst Wagner, Lorenzo Aulisa, Jeffrey Hughes, David T Curiel

Open access · goldAbstract read
In one paragraph

Article in Viruses, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
0.6field-weighted citation impact, top 28% 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

1 citing paper in PubMed, 3 citations in OpenAlex.

  1. 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

7 authors at 3 institutions in 2 countries.

Myungeun LeeDivision of Cancer Biology, Department of Radiation Oncology, School of Medicine, Washington University in St. Louis, St. Louis, MO 63110, USA.
Paul J Rice-BoucherDivision of Cancer Biology, Department of Radiation Oncology, School of Medicine, Washington University in St. Louis, St. Louis, MO 63110, USA.
Logan Thrasher CollinsDivision of Cancer Biology, Department of Radiation Oncology, School of Medicine, Washington University in St. Louis, St. Louis, MO 63110, USA.ORCID 0000-0003-1239-4310
Ernst WagnerDepartment of Chemistry and Pharmacy, Ludwig-Maximilians-University (LMU), 81377 Munich, Germany.ORCID 0000-0001-8413-0934
Lorenzo AulisaGreenLight Biosciences, Inc., 200 Boston Ave. #3100, Medford, MA 02155, USA.
Jeffrey HughesGreenLight Biosciences, Inc., 200 Boston Ave. #3100, Medford, MA 02155, USA.
David T CurielDivision of Cancer Biology, Department of Radiation Oncology, School of Medicine, Washington University in St. Louis, St. Louis, MO 63110, USA.ORCID 0000-0003-3802-6014
Washington University in St. Louis · USGreenLight Biosciences (United States) · USLudwig-Maximilians-Universität München · DE

Funding

PRINCIPLES IN PULMONARY RESEARCHT32HL007317 · NHLBI · WASHINGTON UNIVERSITY · PI Steven Brody, Michael J Holtzman · 1985 to 2026
$16.1M
Novel targeted adenovirusR01CA211096 · NCI · WASHINGTON UNIVERSITY · PI CURIEL, DAVID TERRY · 2017 to 2021
$1.7M
NHLBI NIH HHS T32 HL007317NIH HHS R01 CA211096
6 · The paper itself

Abstract

Molecular therapies exploiting mRNA vectors embody enormous potential, as evidenced by the utility of this technology for the context of the COVID-19 pandemic. Nonetheless, broad implementation of these promising strategies has been restricted by the limited repertoires of delivery vehicles capable of mRNA transport. On this basis, we explored a strategy based on exploiting the well characterized entry biology of adenovirus. To this end, we studied an adenovirus-polylysine (AdpL) that embodied "piggyback" transport of the mRNA on the capsid exterior of adenovirus. We hypothesized that the efficient steps of Ad binding, receptor-mediated entry, and capsid-mediated endosome escape could provide an effective pathway for transport of mRNA to the cellular cytosol for transgene expression. Our studies confirmed that AdpL could mediate effective gene transfer of mRNA vectors in vitro and in vivo. Facets of this method may offer key utilities to actualize the promise of mRNA-based therapeutics.

Indexed as

Adenoviridae InfectionsCOVID-19AdenoviridaeBiologyCapsid ProteinsGenetic VectorsGene Transfer TechniquesHumansPandemicsPolylysineRNA, MessengerCapsid ProteinsPolylysineRNA, Messengermessenger Ribonucleic Acid (mRNA)streptavidin-polylysine (STAVpLys)targeted adenoviral vectors (Ad)

Identifiers

PMID36298724
PMCPMC9608319
OpenAlexW4304813812

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.