Evidence map›Paper›PMID 24782509›Full record

Trial reportBlood2014

Closely related T-memory stem cells correlate with in vivo expansion of CAR.CD19-T cells and are preserved by IL-7 and IL-15.

Yang Xu, Ming Zhang, Carlos A Ramos, April Durett, Enli Liu, Olga Dakhova, Hao Liu, Chad J Creighton, Adrian P Gee, Helen E Heslop and 3 more

3 registry-linked trialsAbstract readClinical Trial
In one paragraph

Trial report in Blood, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to 3 registered trials, which are not on this map. Cited by 510 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
510citing papers in PubMed, 1 pooled it
16.3field-weighted citation impact, top 1% 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.

NCT00586391 phase1active not recruitingnot on this map

Phase I Study Of CD19 Chimeric Receptor Expressing T Lymphocytes In B-Cell Non Hodgkin's Lymphoma, Acute Lymphocytic Leukemia, and Chronic Lymphocytic Leukemia

TypeinterventionalSponsorBaylor College of MedicineRan2009 to 2029Enrolled14ConditionsB Cell Lymphoma, Chronic Lymphocytic Leukemia, Acute Lymphocytic LeukemiaArmsCD19CAR-28-zeta T cells, Ipilimumab
NCT00709033 phase1completednot on this map

Phase I Study Of The Administration Of Peripheral Activated T-Cells and EBV Specific CTLs Expressing CD19 Chimeric Receptors For Advanced B-Cell Non-Hodgkin's Lymphoma And Chronic Lymphocytic Leukemia (ATECRAB)

TypeinterventionalSponsorBaylor College of MedicineRan2009 to 2025Enrolled3ConditionsNon-Hodgkin Lymphoma, Chronic Lymphocytic LeukemiaArmsautologous or syngeneic PBTLs and EBV-CTLs
NCT05199311 phase1 / phase2suspendednot on this mapstarted 2022, after this paper: background citation

A Phase I/II Study of Carfilzomib, Iberdomide (CC-220) and Dexamethasone (KID) in Patients With Newly Diagnosed Transplant Eligible Multiple Myeloma

TypeinterventionalSponsorHackensack Meridian HealthRan2022 to 2027Enrolled66ConditionsMultiple MyelomaArmsCarfilzomib, Iberdomide, Oral Dexamethasone
3 · Its place in the literature

Who cites it

510 citing papers in PubMed, 1 synthesis or guideline pooled it, 718 citations in OpenAlex.

  1. Pooled it
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  12. C-terminal CD28 phosphorylation, pY218, modulates IL-2 secretion and therapeutic effect of CAR-T cells.Molecular therapy : the journal of the American Society of Gene Therapy · 2026
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450 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

13 authors at 4 institutions in 1 country.

Yang XuCenter for Cell and Gene Therapy, Department of Pathology and Immunology, Baylor College of Medicine, Houston, TX;
Ming ZhangCenter for Cell and Gene Therapy.
Carlos A RamosCenter for Cell and Gene Therapy, Houston Methodist Hospital, Houston, TX; Department of Medicine, Baylor College of Medicine, Houston, TX;
April DurettCenter for Cell and Gene Therapy.
Enli LiuCenter for Cell and Gene Therapy.
Olga DakhovaCenter for Cell and Gene Therapy.
Hao LiuDan L. Duncan Cancer Center, Division of Biostatistics, Baylor College of Medicine, Houston, TX;
Chad J CreightonDan L. Duncan Cancer Center, Division of Biostatistics, Baylor College of Medicine, Houston, TX;
Adrian P GeeCenter for Cell and Gene Therapy, Department of Pediatrics, Baylor College of Medicine, Houston, TX; and.
Helen E HeslopCenter for Cell and Gene Therapy, Houston Methodist Hospital, Houston, TX; Department of Medicine, Baylor College of Medicine, Houston, TX; Department of Pediatrics, Baylor College of Medicine, Houston, TX; and Texas Children's Hospital, Houston, TX.
Cliona M RooneyCenter for Cell and Gene Therapy, Department of Pathology and Immunology, Baylor College of Medicine, Houston, TX; Department of Pediatrics, Baylor College of Medicine, Houston, TX; and Texas Children's Hospital, Houston, TX.
Barbara SavoldoCenter for Cell and Gene Therapy, Department of Pediatrics, Baylor College of Medicine, Houston, TX; and Texas Children's Hospital, Houston, TX.
Gianpietro DottiCenter for Cell and Gene Therapy, Department of Pathology and Immunology, Baylor College of Medicine, Houston, TX; Department of Medicine, Baylor College of Medicine, Houston, TX; Texas Children's Hospital, Houston, TX.
Baylor College of Medicine · USChildren's Cancer Center · USMethodist Hospital · USTexas Children's Hospital · US

Funding

Tumor BiologyP30CA125123 · NCI · BAYLOR COLLEGE OF MEDICINE · PI DAVID R ROWLEY · 2007 to 2026
$73.9M
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
Enhancement of stem cell transplants using CAR.CD30-redirected T lymphocytesR01HL114564 · NHLBI · UNIV OF NORTH CAROLINA CHAPEL HILL · PI SAVOLDO, BARBARA · 2013 to 2017
$2.2M
Combinatorial targeting of melanoma initiating cellsR01CA138188 · NCI · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI FERRONE, SOLDANO · 2008 to 2012
$1.5M
NCI NIH HHS P01 CA094237NCI NIH HHS P30 CA125123NCI NIH HHS P50 CA 126752NCI NIH HHS P50 CA126752NCI NIH HHS R01 CA138188NHLBI NIH HHS R01 HL114564PHS HHS R01 1145564
6 · The paper itself

Abstract

Adoptive transfer of T lymphocytes expressing a CD19-specific chimeric antigen receptor (CAR.CD19) induces complete tumor regression in patients with lymphoid malignancies. Although in vivo persistence of CAR-T cells correlates with clinical responses, it remains unknown whether specific cell subsets within the CAR-T-cell product correlate with their subsequent in vivo expansion and persistence. We analyzed 14 patients with B-cell malignancies infused with autologous CAR.CD19-redirected T cells expanded ex vivo using IL-2, and found that their in vivo expansion only correlated with the frequency within the infused product of a CD8(+)CD45RA(+)CCR7(+) subset, whose phenotype is closest to "T-memory stem cells." Preclinical models showed that increasing the frequency of CD8(+)CD45RA(+)CCR7(+) CAR-T cells in the infused line by culturing the cells with IL-7 and IL-15 produced greater antitumor activity of CAR-T cells mediated by increased resistance to cell death, following repetitive encounters with the antigen, while preserving their migration to secondary lymphoid organs. This trial was registered at www.clinicaltrials.gov as #NCT00586391 and #NCT00709033.

Indexed as

Immunologic MemoryAdoptive TransferAdult Stem CellsAnimalsAntigens, CD19Cell ProliferationCells, CulturedGenetic TherapyHumansInterleukin-15Interleukin-7Lymphocyte ActivationLymphomaMiceMice, SCIDMice, TransgenicAntigens, CD19Interleukin-15Interleukin-7Receptors, AntigenRecombinant Fusion Proteins

Identifiers

PMID24782509
PMCPMC4055922
OpenAlexW1982795546

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

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.