Evidence map›Paper›PMID 24215295›Full record

ArticleBMC biotechnology2013

Simplified production and concentration of lentiviral vectors to achieve high transduction in primary human T cells.

Adam P Cribbs, Alan Kennedy, Bernard Gregory, Fionula M Brennan

Abstract read
In one paragraph

Article in BMC biotechnology, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 70 papers.

0numbers the graph read from it
0cells of the map it votes in
70citing 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

70 citing papers in PubMed.

  1. Article
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  7. Enhancing titers of therapeutic lentiviral vectors using PKC agonists.Molecular therapy. Methods & clinical development · 2025
    Article
  8. Review
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  19. Measurement of CaMethods in molecular biology (Clifton, N.J.) · 2024
    Article
  20. Regulation of PPARγ2 Stability and Activity by SHP-1.Molecular and cellular biology · 2024
    Article

10 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

4 authors.

Adam P CribbsKennedy Institute of Rheumatology, Roosevelt Drive, Headington OX3 7FY, Oxford, UK. adam.cribbs@kennedy.ox.ac.uk.
Alan Kennedy
Bernard Gregory
Fionula M Brennan

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundLentiviral vectors have emerged as efficient vehicles for transgene delivery in both dividing and non-dividing cells. A number of different modifications in vector design have increased biosafety and transgene expression. However, despite these advances, the transduction of primary human T cells is still challenging and methods to achieve efficient gene transfer are often expensive and time-consuming.

resultsHere we present a simple optimised protocol for the generation and transduction of lentivirus in primary human CD45RA+ T cells. We show that generation of high-titre lentivirus with improved primary T cell transduction is dependent upon optimised ultracentrifuge speed during viral concentration. Moreover, we demonstrate that transduction efficiency can be increased with simple modifications to the culturing conditions. Overall, a transduction efficiency of up to 89% in primary human CD45RA+ cells is achievable when these modifications are used in conjunction.

conclusionThe optimised protocol described here is easy to implement and should facilitate the production of high-titre lentivirus with superior transduction efficiency in primary human T cells without the need for further purification methods.

Indexed as

Butyric AcidCalcium PhosphatesGenetic VectorsGene Transfer TechniquesHEK293 CellsHumansLentivirusLeukocyte Common AntigensLipidsPlasmidsT-LymphocytesTransduction, GeneticTransfectionTransgenesButyric Acidcalcium phosphateCalcium PhosphatesLeukocyte Common AntigensLipidsLipofectamine

Identifiers

PMID24215295
PMCPMC3830501

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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.