Evidence map›Paper›PMID 35152995›Full record

ArticleMethods in cell biology2022

Generation of CAR T-cells using γ-retroviral vector.

Norihiro Watanabe, Mary Kathryn McKenna

Open access · greenAbstract read
In one paragraph

Article in Methods in cell biology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
9.9field-weighted citation impact, top 2% 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

17 citing papers in PubMed, 14 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Review
  5. Article
  6. Review
  7. Review
  8. Article
  9. Review
  10. Strategies for Altering Delivery Technologies to Optimize CAR Therapy.International journal of molecular sciences · 2025
    Review
  11. Article
  12. Review
  13. Article
  14. Metabolic priming of GD2Molecular therapy. Methods & clinical development · 2024
    Article
  15. Frontiers in immunology · 2024
    Article
  16. Review
  17. Review
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 at 1 institution in 1 country.

Norihiro WatanabeCenter for Cell and Gene Therapy, Baylor College of Medicine, Houston, TX, United States. Electronic address: nwatanab@bcm.edu.
Mary Kathryn McKennaCenter for Cell and Gene Therapy, Baylor College of Medicine, Houston, TX, United States.
Baylor College of Medicine · US

Funding

Training In Cell and Gene TherapyT32HL092332 · NHLBI · BAYLOR COLLEGE OF MEDICINE · PI MALCOLM K. BRENNER, Bruno Di Stefano · 2008 to 2026
$6.9M
NHLBI NIH HHS T32 HL092332
6 · The paper itself

Abstract

The generation of chimeric antigen receptor (CAR) T cells requires the transfer of the CAR gene into primary T cells. Among various gene transfer strategies, gammaretroviral vectors have been widely used to generate CAR T cells for both preclinical and clinical settings. Here we describe the detailed method of generating CAR T cells utilizing gammaretroviral vectors. This approach consists of two parallel parts: (1) production of the gammaretroviral particles and (2) gammaretroviral transduction of activated T cells. The gammaretroviral particles are produced by co-transfecting the gammaretroviral vector with packaging plasmids into 293T cells. The manufactured viral particles then efficiently infect activated T cells where the CAR transgene is integrated into host genomic DNA, resulting in stable expression of the CAR molecule on the surface of T cells.

Indexed as

Genetic VectorsReceptors, Antigen, T-CellPlasmidsT-LymphocytesTransgenesReceptors, Antigen, T-CellChimeric antigen receptorsGammaretroviral vectorsT cell transduction

Identifiers

PMID35152995
PMCPMC8917789
OpenAlexW4210994509

What OpenQuestion holds

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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.