Evidence map›Paper›PMID 18632744›Full record

ReviewBriefings in functional genomics & proteomics2008

Strategies for manufacturing recombinant adeno-associated virus vectors for gene therapy applications exploiting baculovirus technology.

Alejandro Negrete, Robert M Kotin

Abstract readReview
In one paragraph

Review in Briefings in functional genomics & proteomics, 2008. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing 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

10 citing papers in PubMed.

  1. Trial
  2. Review
  3. Evolving membrane-associated accessory protein variants for improved adeno-associated virus production.Molecular therapy : the journal of the American Society of Gene Therapy · 2024
    Article
  4. Article
  5. Review
  6. Article
  7. Article
  8. Article
  9. Review
  10. 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

2 authors.

Alejandro NegreteBirmingham University, UK.
Robert M Kotin

Funding

Recombinant Adeno Associated Virus Vectors for Gene TransferZIAHL002237 · NHLBI · NATIONAL HEART, LUNG, AND BLOOD INSTITUTE · PI KOTIN, ROBERT · 2009 to 2014
$11.7M
RECOMBINANT ADENO-ASSOCIATED VIRUSZ01HL002237 · NHLBI · NATIONAL HEART, LUNG, AND BLOOD INSTITUTE · PI KOTIN, ROBERT · 1995 to 2008
$3.8M
Intramural NIH HHS Z01 HL002237Intramural NIH HHS Z99 HL999999
6 · The paper itself

Abstract

The development of recombinant adeno-associated virus (rAAV) gene therapy applications is hampered by the inability to produce rAAV in sufficient quantities to support pre-clinical and clinical trials. Contrasting with adherent cell cultures, suspension cultures provide a straightforward means for expansion, however, transiently expressing the necessary, but cytotoxic virus proteins remains the challenge for rAAV production. Both the expansion and expression issues are resolved by using the baculovirus expression vector (bev) and insect cell culture system. This review addresses strategies for the production of rAAV exploiting baculovirus technology at different scales using different configurations of bioreactors as well as processing and product characterization issues. The yields obtained with these optimized processes exceed approximately 1 x 10(14) vector particles per liter of cell culture suitable for pre-clinical and clinical trials and possible commercialization.

Indexed as

Genetic VectorsRecombination, GeneticAnimalsBaculoviridaeBioreactorsCloning, MolecularDependovirusGenetic TherapyGene Transfer TechniquesInsectaSimplexvirusTransduction, Genetic

Identifiers

PMID18632744
PMCPMC2562640

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.