Evidence map›Paper›PMID 20561357›Full record

ReviewImmunology2010

Molecular immunology lessons from therapeutic T-cell receptor gene transfer.

Sharyn Thomas, Hans J Stauss, Emma C Morris

Open access · greenAbstract readReview
In one paragraph

Review in Immunology, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 30 papers.

0numbers the graph read from it
0cells of the map it votes in
30citing papers in PubMed
3.2field-weighted citation impact, top 8% 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

30 citing papers in PubMed, 47 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Evolution of CD8Cells · 2021
    Review
  5. Article
  6. Article
  7. Review
  8. T Cell Reprogramming Against Cancer.Methods in molecular biology (Clifton, N.J.) · 2020
    Review
  9. Review
  10. Preclinical Strategies to Identify Off-Target Toxicity of High-Affinity TCRs.Molecular therapy : the journal of the American Society of Gene Therapy · 2018
    Article
  11. Article
  12. Review
  13. Article
  14. Article
  15. Seatbelts in CAR therapy: How Safe Are CARS?Pharmaceuticals (Basel, Switzerland) · 2015
    Review
  16. Article
  17. Review
  18. T cell avidity and tumor immunity: problems and solutions.Cancer microenvironment : official journal of the International Cancer Microenvironment Society · 2014
    Article
  19. 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

3 authors at 2 institutions in 1 country.

Sharyn ThomasDepartment of Immunology and Molecular Pathology, Division of Infection and Immunity, UCL Medical School, Royal Free Hospital, London, UK.
Hans J Stauss
Emma C Morris
University College London · GBThe Royal Free Hospital · GB

Funding

Medical Research Council G0900950Medical Research Council G0902209Medical Research Council G9721629
6 · The paper itself

Abstract

The T-cell receptor (TCR) is critical for T-cell lineage selection, antigen specificity, effector function and survival. Recently, TCR gene transfer has been developed as a reliable method to generate ex vivo large numbers of T cells of a given antigen-specificity and functional avidity. Such approaches have major applications for the adoptive cellular therapy of viral infectious diseases, virus-associated malignancies and cancer. TCR gene transfer utilizes retroviral or lentiviral constructs containing the gene sequences of the TCR-alpha and TCR-beta chains, which have been cloned from a clonal T-cell population of the desired antigen specificity. The TCR-encoding vector is then used to infect (transduce) primary T cells in vitro. To generate a transduced T cell with the desired functional specificity, the introduced TCR-alpha and TCR-beta chains must form a heterodimer and associate with the CD3 complex in order to be stably expressed at the T-cell surface. In order to optimize the function of TCR-transduced T cells, researchers in the field of TCR gene transfer have exploited many aspects of basic research in T-cell immunology relating to TCR structure, TCR-CD3 assembly, cell-surface TCR expression, TCR-peptide/major histocompatibility complex (MHC) affinity and TCR signalling. However, improving the introduction of exogenous TCRs into naturally occurring T cells has provided further insights into basic T-cell immunology. The aim of this review was to discuss the molecular immunology lessons learnt through therapeutic TCR transfer.

Indexed as

Immunotherapy, AdoptiveTransduction, GeneticAnimalsCommunicable DiseasesGenetic TherapyGene Transfer TechniquesHumansNeoplasmsReceptors, Antigen, T-CellT-LymphocytesT-Lymphocyte SubsetsReceptors, Antigen, T-Cell

Identifiers

PMID20561357
PMCPMC2814459
OpenAlexW1993717518

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.