Evidence map›Paper›PMID 20200563›Full record

ArticleGene therapy2010

Gene-modified T cells as immunotherapy for multiple myeloma and acute myeloid leukemia expressing the Lewis Y antigen.

S Peinert, H M Prince, P M Guru, M H Kershaw, M J Smyth, J A Trapani, P Gambell, S Harrison, A M Scott, F E Smyth and 5 more

Abstract read
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In one paragraph

Article in Gene therapy, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 79 papers.

0numbers the graph read from it
0cells of the map it votes in
79citing papers in PubMed
2.7field-weighted citation impact, top 10% 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

79 citing papers in PubMed, 118 citations in OpenAlex.

  1. Article
  2. Review
  3. Review
  4. Review
  5. Targets for CAR Therapy in Multiple Myeloma.International journal of molecular sciences · 2025
    Review
  6. Article
  7. Article
  8. Review
  9. Recent advances of CAR-T cells in acute myeloid leukemia.Therapeutic advances in hematology · 2025
    Review
  10. Review
  11. Review
  12. Review
  13. Recent advances in CAR-T cell therapy for acute myeloid leukaemia.Journal of cellular and molecular medicine · 2024
    Review
  14. Review
  15. Review
  16. Review
  17. Review
  18. Article
  19. Article
  20. Review

19 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

15 authors at 4 institutions in 1 country.

S PeinertDepartment of Haematology and Medical Oncology, Peter MacCallum Cancer Centre, Victoria, Australia. stefan.peinert@petermac.org
H M Prince
P M Guru
M H Kershaw
M J Smyth
J A Trapani
P Gambell
S Harrison
A M Scott
F E Smyth
P K Darcy
K Tainton
P Neeson
D S Ritchie
D Hönemann
Peter MacCallum Cancer Centre · AUUniversity of Melbourne · AUAustin Hospital · AULudwig Cancer Research · AU

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

We have evaluated the carbohydrate antigen Lewis(Y) (Le(Y)) as a potential target for T-cell immunotherapy of hematological neoplasias. Analysis of 81 primary bone marrow samples revealed moderate Le(Y) expression on plasma cells of myeloma patients and myeloblasts of patients with acute myeloid leukemia (AML) (52 and 46% of cases, respectively). We developed a retroviral vector construct encoding a chimeric T-cell receptor that recognizes the Le(Y) antigen in a major histocompatibility complex-independent manner and delivers co-stimulatory signals to achieve T-cell activation. We have shown efficient transduction of peripheral blood-derived T cells with this construct, resulting in antigen-restricted interferon-gamma secretion and cell lysis of Le(Y)-expressing tumor cells. In vivo activity of gene-modified T cells was demonstrated in the delayed growth of myeloma xenografts in NOD/SCID mice, which prolonged survival. Therefore, targeting Le(Y)-positive malignant cells with T cells expressing a chimeric receptor recognizing Le(Y) was effective both in vitro and in a myeloma mouse model. Consequently, we plan to use T cells manufactured under Good Manufacturing Practice conditions in a phase I immunotherapy study for patients with Le(Y)-positive myeloma or AML.

Indexed as

AnimalsFemaleGenetic TherapyGenetic VectorsHumansImmunotherapy, AdoptiveInterferon-gammaLeukemia, Myeloid, AcuteLewis Blood Group AntigensLymphocyte ActivationMaleMiceMice, Inbred NODMice, SCIDMultiple MyelomaReceptors, Antigen, T-CellInterferon-gammaLewis Blood Group AntigensLewis Y antigenReceptors, Antigen, T-Cell

Identifiers

PMID20200563
OpenAlexW2005600353

What OpenQuestion holds

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Read underepoch 390

Registered trials

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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.