Evidence map›Paper›PMID 26526988›Full record

ArticleLeukemia2016

Preclinical targeting of human T-cell malignancies using CD4-specific chimeric antigen receptor (CAR)-engineered T cells.

K Pinz, H Liu, M Golightly, A Jares, F Lan, G W Zieve, N Hagag, M Schuster, A E Firor, X Jiang and 1 more

Abstract read
PubMed Publisher
In one paragraph

Article in Leukemia, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 76 papers.

0numbers the graph read from it
0cells of the map it votes in
76citing papers in PubMed
2.9field-weighted citation impact, top 7% 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

76 citing papers in PubMed, 114 citations in OpenAlex.

  1. Review
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  8. Review
  9. Review
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  11. In vivo CAR T cell therapy against angioimmunoblastic T cell lymphoma.Journal of experimental & clinical cancer research : CR · 2024
    Article
  12. Review
  13. Review
  14. Review
  15. Article
  16. Review
  17. Transcriptome Analysis in Mexican Adults with Acute Lymphoblastic Leukemia.International journal of molecular sciences · 2024
    Article
  18. Review
  19. Chimeric antigen receptor T cells march into T cell malignancies.Journal of cancer research and clinical oncology · 2023
    Review
  20. Article

16 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

11 authors at 3 institutions in 2 countries.

K PinzR and D, iCell Gene Therapeutics LLC, Long Island High Technology Incubator, Stony Brook, NY, USA.
H LiuDepartment of Pathology, Stony Brook Medicine, Stony Brook, NY, USA.
M GolightlyDepartment of Pathology, Stony Brook Medicine, Stony Brook, NY, USA.
A JaresDepartment of Pathology, Stony Brook Medicine, Stony Brook, NY, USA.
F LanDepartment of Internal Medicine, Stony Brook Medicine, Stony Brook University Medical Center, Stony Brook, NY, USA.
G W ZieveR and D, iCell Gene Therapeutics LLC, Long Island High Technology Incubator, Stony Brook, NY, USA.
N HagagDepartment of Internal Medicine, Stony Brook Medicine, Stony Brook University Medical Center, Stony Brook, NY, USA.
M SchusterDepartment of Internal Medicine, Stony Brook Medicine, Stony Brook University Medical Center, Stony Brook, NY, USA.
A E FirorR and D, iCell Gene Therapeutics LLC, Long Island High Technology Incubator, Stony Brook, NY, USA.
X JiangR and D, iCell Gene Therapeutics LLC, Long Island High Technology Incubator, Stony Brook, NY, USA.
Y MaR and D, iCell Gene Therapeutics LLC, Long Island High Technology Incubator, Stony Brook, NY, USA.
Stony Brook Medicine · USStony Brook University Hospital · USMacau University of Science and Technology · MO

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Peripheral T-cell lymphomas (PTCLs) are aggressive lymphomas with no effective upfront standard treatment and ineffective options in relapsed disease, resulting in poorer clinical outcomes as compared with B-cell lymphomas. The adoptive transfer of T cells engineered to express chimeric antigen receptors (CARs) is a promising new approach for treatment of hematological malignancies. However, preclinical reports of targeting T-cell lymphoma with CARs are almost non-existent. Here we have designed a CAR, CD4CAR, which redirects the antigen specificity of CD8+ cytotoxic T cells to CD4-expressing cells. CD4CAR T cells derived from human peripheral blood mononuclear cells and cord blood effectively redirected T-cell specificity against CD4+ cells in vitro. CD4CAR T cells efficiently eliminated a CD4+ leukemic cell line and primary CD4+ PTCL patient samples in co-culture assays. Notably, CD4CAR T cells maintained a central memory stem cell-like phenotype (CD8+CD45RO+CD62L+) under standard culture conditions. Furthermore, in aggressive orthotropic T-cell lymphoma models, CD4CAR T cells efficiently suppressed the growth of lymphoma cells while also significantly prolonging mouse survival. Combined, these studies demonstrate that CD4CAR-expressing CD8+ T cells are efficacious in ablating malignant CD4+ populations, with potential use as a bridge to transplant or stand-alone therapy for the treatment of PTCLs.

Indexed as

Adoptive TransferAnimalsCD4-Positive T-LymphocytesCD8-Positive T-LymphocytesCell EngineeringCell Line, TumorCoculture TechniquesCytotoxicity, ImmunologicGene ExpressionHumansLeukemiaLymphoma, T-Cell, PeripheralMaleMiceMice, Inbred NODMutant Chimeric ProteinsMutant Chimeric ProteinsReceptors, Artificial

Identifiers

PMID26526988
OpenAlexW2155781172

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.