Evidence map›Paper›PMID 19434609›Full record

ArticleThe journal of gene medicine2009

Redirecting lentiviral vectors by insertion of integrin-tageting peptides into envelope proteins.

Kouki Morizono, Nonia Pariente, Yiming Xie, Irvin S Y Chen

Open access · greenAbstract read
In one paragraph

Article in The journal of gene medicine, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers.

0numbers the graph read from it
0cells of the map it votes in
21citing papers in PubMed
2.3field-weighted citation impact, top 11% 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

21 citing papers in PubMed, 31 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Review
  5. Envelope protein-specific B cell receptors direct lentiviral vector tropism in vivo.Molecular therapy : the journal of the American Society of Gene Therapy · 2024
    Article
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  18. Receptors and tropisms of envelope viruses.Current opinion in virology · 2011
    Review
  19. DARPins: an efficient targeting domain for lentiviral vectors.Molecular therapy : the journal of the American Society of Gene Therapy · 2011
    Article
  20. 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

4 authors at 2 institutions in 1 country.

Kouki MorizonoDepartment of Medicine, University of California, Los Angeles, 90095, USA.
Nonia Pariente
Yiming Xie
Irvin S Y Chen
Black AIDS Institute · USUniversity of California, Los Angeles · US

Funding

Virology CoreP30AI028697 · NIAID · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI ANTON, PETER A · 1991 to 2018
$39.9M
Retargeting of Retroviral VectorsR01AI069350 · NIAID · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI CHEN, IRVIN S.Y. · 2006 to 2010
$1.7M
PRIMATE LENTIVIRUS BASED THERAPY VECTORSR01AI039975 · NIAID · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI CHEN, IRVIN S.Y. · 1997 to 2005
$1.5M
Control of topoisomerose II through the cell cycleR01CA092194 · NCI · CLEVELAND CLINIC LERNER COL/MED-CWRU · PI STACEY, DENNIS W · 2001 to 2004
$874k
Molecular Imaging of Cancer In vivo via Targeted TransductionR01CA120327 · NCI · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI CHEN, IRVIN S.Y. · 2007 to 2009
$705k
Targeting Gene Delivery to the CNS Blood-Brain BarrierR21NS055212 · NINDS · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI CHEN, IRVIN S.Y. · 2007 to 2008
$372k
NCI NIH HHS CA-92194NCI NIH HHS R01 CA092194NCI NIH HHS R01 CA120327NIAID NIH HHS AI028697NIAID NIH HHS AI039975NIAID NIH HHS AI069350NIAID NIH HHS P30 AI028697NIAID NIH HHS R01 AI039975NIAID NIH HHS R01 AI069350NINDS NIH HHS R21 NS055212
6 · The paper itself

Abstract

backgroundTargeting gene therapy vectors that can home in on desired cell and tissue types in vivo comprise the ultimate gene delivery system. We have previously developed targeting lentiviral vectors by pseudotyping vectors with modified Sindbis virus envelope proteins. The envelope protein contains the Fc-binding region of protein A (ZZ domain), so the virus can be conjugated with antibodies. The conjugated antibody mediates specific transduction of the cells and tissues expressing the target antigens, both in vitro and in vivo. However, more stable conjugation of targeting molecules would be optimal for use in immunocompetent animals, as well as in humans.

methodsWe inserted integrin-targeting peptides into two sites of the targeting envelope proteins and determined whether the peptides serve as receptor-binding regions of the envelope proteins and redirect the pseudotyped viruses.

resultsThe integrin-targeting peptides can mediate binding to cells via the interaction with integrins on target cells and transduction. Peptides with a higher binding affinity increase titers of pseudotyped virus. We found two regions on the envelope protein that can accommodate insertion and serve as receptor-binding regions. Combining the peptides in two distinct regions increased the titers of the virus.

conclusionsSuccessful incorporation of targeting molecules into the envelope protein will broaden the application of targeting vectors for a wide variety of experimental and clinical settings.

Indexed as

Genetic VectorsLentivirusPeptidesViral Envelope ProteinsAnimalsCell LineHumansIntegrinsRecombinant Fusion ProteinsSindbis VirusTransduction, GeneticIntegrinsPeptidesRecombinant Fusion ProteinsViral Envelope Proteins

Identifiers

PMID19434609
PMCPMC2834586
OpenAlexW2047560976

What OpenQuestion holds

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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.