Evidence map›Paper›PMID 31537820›Full record

ArticleScientific reports2019

Production of adeno-associated virus vectors for in vitro and in vivo applications.

Toyokazu Kimura, Beatriz Ferran, Yuko Tsukahara, Qifan Shang, Suveer Desai, Alessandra Fedoce, David Richard Pimentel, Ivan Luptak, Takeshi Adachi, Yasuo Ido and 2 more

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 96 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
96citing papers in PubMed, 1 pooled it
10.6field-weighted citation impact, top 1% 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

96 citing papers in PubMed, 1 synthesis or guideline pooled it, 151 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Lung endothelial cytopathic tau is sufficient to impair long-term potentiation during infection.American journal of respiratory cell and molecular biology · 2026
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  4. Article
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  6. Review
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  9. Journal of the American Heart Association · 2026
    Article
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  14. The adhesion GPCR ADGRL2 engages Gα13 to enable epidermal differentiation.Proceedings of the National Academy of Sciences of the United States of America · 2025
    Article
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  18. Review
  19. Article
  20. Article

36 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

12 authors at 2 institutions in 2 countries.

Toyokazu KimuraVascular Biology Section, Whitaker Cardiovascular Institute, Boston University School of Medicine, Boston, USA.
Beatriz FerranVascular Biology Section, Whitaker Cardiovascular Institute, Boston University School of Medicine, Boston, USA.
Yuko TsukaharaVascular Biology Section, Whitaker Cardiovascular Institute, Boston University School of Medicine, Boston, USA.
Qifan ShangVascular Biology Section, Whitaker Cardiovascular Institute, Boston University School of Medicine, Boston, USA.
Suveer DesaiVascular Biology Section, Whitaker Cardiovascular Institute, Boston University School of Medicine, Boston, USA.
Alessandra FedoceVascular Biology Section, Whitaker Cardiovascular Institute, Boston University School of Medicine, Boston, USA.
David Richard PimentelCardiology, Whitaker Cardiovascular Institute, Boston University School of Medicine, Boston, USA.
Ivan LuptakCardiology, Whitaker Cardiovascular Institute, Boston University School of Medicine, Boston, USA.
Takeshi AdachiCardiovascular Medicine, National Defense Medical College, Tokorozawa, Japan.
Yasuo IdoCardiovascular Medicine, National Defense Medical College, Tokorozawa, Japan.
Reiko MatsuiVascular Biology Section, Whitaker Cardiovascular Institute, Boston University School of Medicine, Boston, USA. rmatsui@bu.edu.ORCID http://orcid.org/0000-0002-8132-2823
Markus Michael BachschmidVascular Biology Section, Whitaker Cardiovascular Institute, Boston University School of Medicine, Boston, USA. bach@bu.edu.ORCID http://orcid.org/0000-0002-0748-5528
Boston University · USNational Defense Medical College · JP

Funding

Project-005UL1TR001430 · NCATS · BOSTON UNIVERSITY MEDICAL CAMPUS · PI BAIR-MERRITT, MEGAN H, CENTER, DAVID M. · 2015 to 2024
$52.3M
Multidisciplinary Training in Cardiovascular ResearchT32HL007224 · NHLBI · BOSTON UNIVERSITY MEDICAL CAMPUS · PI HAMBURG, NAOMI MIRIAM, WAINFORD, RICHARD DAVID · 1985 to 2020
$12.3M
Redox Control of Hepatic Lipid MetabolismR01DK103750 · NIDDK · BOSTON UNIVERSITY MEDICAL CAMPUS · PI BACHSCHMID, MARKUS MICHAEL · 2015 to 2019
$1.8M
Regulation of ischemic limb vascularization by glutaredoxin-1R01HL133013 · NHLBI · BOSTON UNIVERSITY MEDICAL CAMPUS · PI MATSUI, REIKO · 2016 to 2019
$1.6M
Regulation of ischemic vascularization by glutaredoxin-1 by agingR03AG051857 · NIA · BOSTON UNIVERSITY MEDICAL CAMPUS · PI MATSUI, REIKO · 2016 to 2017
$236k
NCATS NIH HHS UL1 TR001430NHLBI NIH HHS R01 HL133013NHLBI NIH HHS T32 HL007224NIA NIH HHS R03 AG051857NIDDK NIH HHS R01 DK103750
6 · The paper itself

Abstract

Delivering and expressing a gene of interest in cells or living animals has become a pivotal technique in biomedical research and gene therapy. Among viral delivery systems, adeno-associated viruses (AAVs) are relatively safe and demonstrate high gene transfer efficiency, low immunogenicity, stable long-term expression, and selective tissue tropism. Combined with modern gene technologies, such as cell-specific promoters, the Cre/lox system, and genome editing, AAVs represent a practical, rapid, and economical alternative to conditional knockout and transgenic mouse models. However, major obstacles remain for widespread AAV utilization, such as impractical purification strategies and low viral quantities. Here, we report an improved protocol to produce serotype-independent purified AAVs economically. Using a helper-free AAV system, we purified AAVs from HEK293T cell lysates and medium by polyethylene glycol precipitation with subsequent aqueous two-phase partitioning. Furthermore, we then implemented an iodixanol gradient purification, which resulted in preparations with purities adequate for in vivo use. Of note, we achieved titers of 10

Indexed as

AnimalsCell LineChemical PrecipitationDependovirusDown-RegulationGenetic VectorsGlutaredoxinsHEK293 CellsHumansLiverMaleMuscle, SkeletalPolyethylenesProof of Concept StudyRNA, Small InterferingTransduction, GeneticGlrx protein, mouseGlutaredoxinspolyethylene chloridePolyethylenesRNA, Small Interfering

Identifiers

PMID31537820
PMCPMC6753157
OpenAlexW2973390883

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.