Evidence map›Paper›PMID 38298420›Full record

ArticleMolecular therapy. Methods & clinical development2024

Manufacture of CD22 CAR T cells following positive versus negative selection results in distinct cytokine secretion profiles and γδ T cell output.

Hannah W Song, Mehdi Benzaoui, Alka Dwivedi, Sarah Underwood, Lipei Shao, Sooraj Achar, Vesna Posarac, Victoria A Remley, Michaela Prochazkova, Yihua Cai and 8 more

Open access · goldAbstract read
In one paragraph

Article in Molecular therapy. Methods & clinical development, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
2.1field-weighted citation impact, top 11% 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

12 citing papers in PubMed, 9 citations in OpenAlex.

  1. CD27 Agonist Antibodies Mediate Clinical Responses through Intratumoral Stimulation in B-cell Malignancies: Multicenter RiVa Trial.Clinical cancer research : an official journal of the American Association for Cancer Research · 2025
    Trial
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  11. Biomanufacturing in gene and cell therapy.Molecular therapy. Methods & clinical development · 2024
    Article
  12. A positive take on negative selection for CAR-T manufacturing.Molecular therapy. Methods & clinical development · 2024
    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

18 authors at 4 institutions in 3 countries.

Hannah W SongCenter for Cellular Engineering, Department of Transfusion Medicine, National Institutes of Health, Bethesda, MD, USA.
Mehdi BenzaouiPediatric Oncology Branch, National Cancer Institute, National Institutes of Health, Bethesda, MD, USA.
Alka DwivediPediatric Oncology Branch, National Cancer Institute, National Institutes of Health, Bethesda, MD, USA.
Sarah UnderwoodCenter for Cellular Engineering, Department of Transfusion Medicine, National Institutes of Health, Bethesda, MD, USA.
Lipei ShaoCenter for Cellular Engineering, Department of Transfusion Medicine, National Institutes of Health, Bethesda, MD, USA.
Sooraj AcharLaboratory of Integrative Cancer Immunology, NCI, Bethesda, MD, USA.
Vesna PosaracSTEMCELL Technologies, Vancouver, Canada.
Victoria A RemleyCenter for Cellular Engineering, Department of Transfusion Medicine, National Institutes of Health, Bethesda, MD, USA.
Michaela ProchazkovaCenter for Cellular Engineering, Department of Transfusion Medicine, National Institutes of Health, Bethesda, MD, USA.
Yihua CaiCenter for Cellular Engineering, Department of Transfusion Medicine, National Institutes of Health, Bethesda, MD, USA.
Ping JinCenter for Cellular Engineering, Department of Transfusion Medicine, National Institutes of Health, Bethesda, MD, USA.
Robert P SomervilleCenter for Cellular Engineering, Department of Transfusion Medicine, National Institutes of Health, Bethesda, MD, USA.
David F StroncekCenter for Cellular Engineering, Department of Transfusion Medicine, National Institutes of Health, Bethesda, MD, USA.
Grégoire Altan-BonnetLaboratory of Integrative Cancer Immunology, NCI, Bethesda, MD, USA.
Nirali N ShahPediatric Oncology Branch, National Cancer Institute, National Institutes of Health, Bethesda, MD, USA.
Christopher D ChienPediatric Oncology Branch, National Cancer Institute, National Institutes of Health, Bethesda, MD, USA.
Naomi TaylorPediatric Oncology Branch, National Cancer Institute, National Institutes of Health, Bethesda, MD, USA.
Steven L HighfillCenter for Cellular Engineering, Department of Transfusion Medicine, National Institutes of Health, Bethesda, MD, USA.
National Institutes of Health · USCentre National de la Recherche Scientifique · FRLaboratoire d’immunologie intégrative du cancer · FRStemcell Technologies · CA

Funding

Metabolic regulation of T cell effector function and anti-tumor immunotherapyZIABC011923 · NCI · DIVISION OF BASIC SCIENCES - NCI · PI TAYLOR, NAOMI · 2019 to 2025
$9.5M
Immunotherapeutic approaches to treat pediatric hematologic malignanciesZIABC011823 · NCI · DIVISION OF BASIC SCIENCES - NCI · PI SHAH, NIRALI · 2019 to 2025
$6.1M
Phenotypic variability within isogenic population of lymphocytesZIABC011726 · NCI · DIVISION OF BASIC SCIENCES - NCI · PI ALTAN-BONNET, GRÉGOIRE · 2016 to 2025
$3.9M
Immunophenotyping by high-dimensional cytometry and machine learningZIABC011807 · NCI · DIVISION OF BASIC SCIENCES - NCI · PI ALTAN-BONNET, GRÉGOIRE · 2018 to 2025
$3.6M
Comprehensive Interrogation of Toxicity Profiles Associated with Novel CAR T-cell ConstructsZIABC012187 · NCI · DIVISION OF BASIC SCIENCES - NCI · PI SHAH, NIRALI · 2024 to 2025
$1.6M
Intramural NIH HHS Z99 CL999999Intramural NIH HHS ZIA BC011807Intramural NIH HHS ZIA BC011923
6 · The paper itself

Abstract

Chimeric antigen receptor T cells (CART) have demonstrated curative potential for hematological malignancies, but the optimal manufacturing has not yet been determined and may differ across products. The first step, T cell selection, removes contaminating cell types that can potentially suppress T cell expansion and transduction. While positive selection of CD4/CD8 T cells after leukapheresis is often used in clinical trials, it may modulate signaling cascades downstream of these co-receptors; indeed, the addition of a CD4/CD8-positive selection step altered CD22 CART potency and toxicity in patients. While negative selection may avoid this drawback, it is virtually absent from good manufacturing practices. Here, we performed both CD4/CD8-positive and -negative clinical scale selections of mononuclear cell apheresis products and generated CD22 CARTs per our ongoing clinical trial (NCT02315612NCT02315612). While the selection process did not yield differences in CART expansion or transduction, positively selected CART exhibited a significantly higher

Indexed as

B-ALLCAR T cell manufacturingCD22 CARchimeric antigen receptorcytokinesnegative selectionpositive selectionT cell selectionγδ T cells

Identifiers

PMID38298420
PMCPMC10827561
OpenAlexW4389568253

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.