Evidence map›Paper›PMID 30889381›Full record

ArticleCancer cell2019

CD40 Ligand-Modified Chimeric Antigen Receptor T Cells Enhance Antitumor Function by Eliciting an Endogenous Antitumor Response.

Nicholas F Kuhn, Terence J Purdon, Dayenne G van Leeuwen, Andrea V Lopez, Kevin J Curran, Anthony F Daniyan, Renier J Brentjens

Open access · bronzeAbstract read
In one paragraph

Article in Cancer cell, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 178 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
178citing papers in PubMed, 2 pooled it
11.9field-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.

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

178 citing papers in PubMed, 2 syntheses or guidelines pooled it, 231 citations in OpenAlex.

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118 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

7 authors at 1 institution in 1 country.

Nicholas F KuhnLouis V. Gerstner Jr. Graduate School of Biomedical Sciences, Memorial Sloan Kettering Cancer Center, New York, NY 10065, USA; Department of Medicine, Memorial Sloan Kettering Cancer Center, New York, NY 10065, USA.
Terence J PurdonDepartment of Medicine, Memorial Sloan Kettering Cancer Center, New York, NY 10065, USA.
Dayenne G van LeeuwenDepartment of Medicine, Memorial Sloan Kettering Cancer Center, New York, NY 10065, USA.
Andrea V LopezDepartment of Medicine, Memorial Sloan Kettering Cancer Center, New York, NY 10065, USA.
Kevin J CurranDepartment of Pediatrics, Memorial Sloan Kettering Cancer Center, New York, NY 10065, USA.
Anthony F DaniyanDepartment of Medicine, Memorial Sloan Kettering Cancer Center, New York, NY 10065, USA.
Renier J BrentjensDepartment of Medicine, Memorial Sloan Kettering Cancer Center, New York, NY 10065, USA. Electronic address: brentjer@mskcc.org.
Memorial Sloan Kettering Cancer Center · US

Funding

X-RAY CRYSTALLOGRAPHYP30CA008748 · NCI · SLOAN-KETTERING INSTITUTE FOR CANCER RES · PI Nicholas D Socci · 1985 to 2026
$347.4M
TUMORICIDAL FUNCTIONS OF T LYMPHOCYTES IN PSMA TUMORSP01CA059350 · NCI · SLOAN-KETTERING INSTITUTE FOR CANCER RES · PI O'REILLY, RICHARD JOHN · 1992 to 2012
$21.4M
Translating Stress Response Targeted Therapy for B-Cell LymphomasP50CA192937 · NCI · SLOAN-KETTERING INST CAN RESEARCH · PI ZELENETZ, ANDREW D. · 2016 to 2020
$10.9M
Personalized Immunotherapy of Patients with Ovarian CancerP01CA190174 · NCI · SLOAN-KETTERING INST CAN RESEARCH · PI SABBATINI, PAUL J, SPRIGGS, DAVID R · 2015 to 2019
$10.5M
MSK Paul Calabresi Career Development Award for Clinical OncologyK12CA184746 · NCI · SLOAN-KETTERING INST CAN RESEARCH · PI Omar Abdel-Wahab, Simon N. Powell · 2015 to 2026
$8.3M
Adoptive Immunotherapy of Cancer with IL-12 Secreting Tumor-Targeted T cellsR01CA138738 · NCI · SLOAN-KETTERING INST CAN RESEARCH · PI BRENTJENS, RENIER JOSEPH · 2009 to 2013
$3.9M
CD40L-Modified Chimeric Antigen Receptor (CAR) T CellsF31CA213668 · NCI · SLOAN-KETTERING INST CAN RESEARCH · PI KUHN, NICHOLAS F · 2017 to 2019
$121k
NCI NIH HHS F31 CA213668NCI NIH HHS K12 CA184746NCI NIH HHS P01 CA059350NCI NIH HHS P01 CA190174NCI NIH HHS P30 CA008748NCI NIH HHS P50 CA192937NCI NIH HHS R01 CA138738
6 · The paper itself

Abstract

Chimeric antigen receptor (CAR) T cells provide great efficacy in B cell malignancies. However, improved CAR T cell therapies are still needed. Here, we engineered tumor-targeted CAR T cells to constitutively express the immune-stimulatory molecule CD40 ligand (CD40L) and explored efficacy in different mouse leukemia/lymphoma models. We observed that CD40L

Indexed as

AnimalsAntigen-Presenting CellsCD40 LigandCell Line, TumorHumansImmunotherapy, AdoptiveMiceMice, Inbred BALB CNeoplasmsReceptors, Chimeric AntigenTumor EscapeXenograft Model Antitumor AssaysCD40 LigandReceptors, Chimeric Antigenantigen-presenting cellsCAR T cellsCD40CD40 ligandchimeric antigen receptorendogenous T cellsimmunotherapyleukemialymphoma

Identifiers

PMID30889381
PMCPMC6428219
OpenAlexW2922068441

What OpenQuestion holds

Textmetadata
LicenceTDM
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.