Evidence map›Paper›PMID 22297819›Full record

ArticleMolecular therapy : the journal of the American Society of Gene Therapy2012

Replication-competent retroviruses in gene-modified T cells used in clinical trials: is it time to revise the testing requirements?

Adham S Bear, Richard A Morgan, Kenneth Cornetta, Carl H June, Gwendolyn Binder-Scholl, Mark E Dudley, Steven A Feldman, Steven A Rosenberg, Sheila A Shurtleff, Cliona M Rooney and 2 more

Abstract read
In one paragraph

Article in Molecular therapy : the journal of the American Society of Gene Therapy, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 34 papers.

0numbers the graph read from it
0cells of the map it votes in
34citing 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

34 citing papers in PubMed.

  1. Review
  2. Review
  3. Review
  4. Long-term stability of clinical-grade lentiviral vectors for cell therapy.Molecular therapy. Methods & clinical development · 2024
    Article
  5. CAR T cells for hematological malignancies.The Journal of clinical investigation · 2024
    Article
  6. Article
  7. Delivery of gene editing therapeutics.Nanomedicine : nanotechnology, biology, and medicine · 2023
    Review
  8. Article
  9. Review
  10. Article
  11. Article
  12. Article
  13. Lipid- and Polymer-Based Nanoparticle Systems for the Delivery of CRISPR/Cas9.Journal of drug delivery science and technology · 2021
    Article
  14. CAR T Cell Therapy for Solid Tumors: Bright Future or Dark Reality?Molecular therapy : the journal of the American Society of Gene Therapy · 2020
    Review
  15. Gene editing for immune cell therapies.Nature biotechnology · 2019
    Review
  16. Article
  17. Review
  18. Absence of Replication-Competent Retrovirus in Vectors, T Cell Products, and Patient Follow-Up Samples.Molecular therapy : the journal of the American Society of Gene Therapy · 2018
    Article
  19. Seek and You Will Not Find: Ending the Hunt for Replication-Competent Retroviruses during Human Gene Therapy.Molecular therapy : the journal of the American Society of Gene Therapy · 2018
    Article
  20. Retroviral and Lentiviral Safety Analysis of Gene-Modified T Cell Products and Infused HIV and Oncology Patients.Molecular therapy : the journal of the American Society of Gene Therapy · 2018
    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

12 authors.

Adham S BearCenter for Cell and Gene Therapy, Baylor College of Medicine, Texas Children's Hospital and The Methodist Hospital, Houston, Texas 77030, USA.
Richard A Morgan
Kenneth Cornetta
Carl H June
Gwendolyn Binder-Scholl
Mark E Dudley
Steven A Feldman
Steven A Rosenberg
Sheila A Shurtleff
Cliona M Rooney
Helen E Heslop
Gianpietro Dotti

Funding

Gene therapy of cancerZIABC010985 · NCI · DIVISION OF BASIC SCIENCES - NCI · PI ROSENBERG, STEVEN · 2009 to 2025
$56.8M
Tissue ResourceP50CA126752 · NCI · BAYLOR COLLEGE OF MEDICINE · PI MALCOLM K. BRENNER, HELEN E HESLOP · 2007 to 2026
$51.4M
VECTOR PRODUCTIONP01CA094237 · NCI · BAYLOR COLLEGE OF MEDICINE · PI HESLOP, HELEN E, ROONEY, CLIONA M. · 2002 to 2017
$27.8M
Clinical production of viral vectors for cancer gene therapyZICBC010989 · NCI · DIVISION OF BASIC SCIENCES - NCI · PI BEYER, RACHEL · 2009 to 2025
$12.6M
Validation of Suicide Strategies for Cellular TherapyU54HL081007 · NHLBI · BAYLOR COLLEGE OF MEDICINE · PI BRENNER, MALCOLM K. · 2005 to 2009
$10.2M
Training In Cell and Gene TherapyT32HL092332 · NHLBI · BAYLOR COLLEGE OF MEDICINE · PI MALCOLM K. BRENNER, Bruno Di Stefano · 2008 to 2026
$6.9M
Cell Production Facility CoreZICBC011020 · NCI · DIVISION OF BASIC SCIENCES - NCI · PI DUDLEY, MARK · 2009 to 2013
$6.5M
National Gene Vector Biorepository and Coordinating Center at Indiana UniversityP40HL116242 · NHLBI · INDIANA UNIVERSITY INDIANAPOLIS · PI CORNETTA, KENNETH · 2012 to 2017
$5.5M
National Gene Vector Biorespository and Coordinating Center at Indiana UniversityP40RR024928 · NCRR · INDIANA UNIVERSITY INDIANAPOLIS · PI CORNETTA, KENNETH · 2008 to 2011
$4.0M
NCI NIH HHS 3P50CA126752NCI NIH HHS P01 CA094237NCI NIH HHS P01CA094237NCI NIH HHS P50 CA126752NCRR NIH HHS P40 RR024928NHLBI NIH HHS 5U54HL081007NHLBI NIH HHS P40 HL116242NHLBI NIH HHS T32 HL092332NHLBI NIH HHS U54 HL081007
6 · The paper itself

Abstract

PubMed holds no abstract for this paper.

Indexed as

AnimalsCell LineClinical Trials as TopicGenetic TherapyGenetic VectorsHumansRetroviridaeT-LymphocytesToxicity TestsTransduction, GeneticVirus Replication

Identifiers

PMID22297819
PMCPMC3277217

What OpenQuestion holds

Textmetadata
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.