Evidence map›Paper›PMID 37258040›Full record

ArticleJournal for immunotherapy of cancer2023

Single CAR-T cell treatment controls disseminated ovarian cancer in a syngeneic mouse model.

Diana Rose E Ranoa, Preeti Sharma, Claire P Schane, Amber N Lewis, Edward Valdez, Venkata V V R Marada, Marlies V Hager, Will Montgomery, Steven P Wolf, Karin Schreiber and 6 more

Open access · goldAbstract read
In one paragraph

Article in Journal for immunotherapy of cancer, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
2.8field-weighted citation impact, top 9% 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

9 citing papers in PubMed, 12 citations in OpenAlex.

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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

16 authors at 3 institutions in 1 country.

Diana Rose E RanoaCarl R. Woese Institute for Genomic Biology and Cancer Center at Illinois, University of Illinois at Urbana-Champaign, Urbana, Illinois, USA.ORCID 0000-0002-2363-6111
Preeti SharmaDepartment of Biochemistry, University of Illinois at Urbana-Champaign, Urbana, Illinois, USA.
Claire P SchaneDepartment of Biochemistry, University of Illinois at Urbana-Champaign, Urbana, Illinois, USA.
Amber N LewisDepartment of Biochemistry, University of Illinois at Urbana-Champaign, Urbana, Illinois, USA.ORCID 0009-0008-3651-9062
Edward ValdezDepartment of Biochemistry, University of Illinois at Urbana-Champaign, Urbana, Illinois, USA.
Venkata V V R MaradaDepartment of Biochemistry, University of Illinois at Urbana-Champaign, Urbana, Illinois, USA.
Marlies V HagerDepartment of Biochemistry, University of Illinois at Urbana-Champaign, Urbana, Illinois, USA.
Will MontgomeryCarl R. Woese Institute for Genomic Biology, University of Illinois at Urbana-Champaign, Urbana, Illinois, USA.
Steven P WolfDepartment of Pathology and David and Etta Jonas Center for Cellular Therapy, The University of Chicago, Chicago, Illinois, USA.
Karin SchreiberDepartment of Pathology and David and Etta Jonas Center for Cellular Therapy, The University of Chicago, Chicago, Illinois, USA.
Hans SchreiberDepartment of Pathology and David and Etta Jonas Center for Cellular Therapy, The University of Chicago, Chicago, Illinois, USA.
Keith BaileyCharles River Laboratories Inc Mattawan, Mattawan, Michigan, USA.
Timothy M FanCarl R. Woese Institute for Genomic Biology and Cancer Center at Illinois, University of Illinois at Urbana-Champaign, Urbana, Illinois, USA.
Paul J HergenrotherCarl R. Woese Institute for Genomic Biology and Cancer Center at Illinois, University of Illinois at Urbana-Champaign, Urbana, Illinois, USA.
Edward J RoyCarl R. Woese Institute for Genomic Biology and Cancer Center at Illinois, University of Illinois at Urbana-Champaign, Urbana, Illinois, USA.
David M KranzCarl R. Woese Institute for Genomic Biology and Cancer Center at Illinois, University of Illinois at Urbana-Champaign, Urbana, Illinois, USA d-kranz@illinois.edu.ORCID 0000-0002-4931-126X
University of Illinois Urbana-Champaign · USUniversity of Chicago · USCharles River Laboratories (United States) · US

Funding

PATHOBIOLOGY OF MYELOMA AND ANTI-IDIOTYPIC IMMUNITYR01CA022677 · NCI · UNIVERSITY OF CHICAGO · PI SCHREIBER, HANS · 1985 to 2024
$6.3M
Small Molecule Activators of Procaspases as Anti-Cancer AgentsR01CA120439 · NCI · UNIVERSITY OF ILLINOIS AT URBANA-CHAMPAIGN · PI HERGENROTHER, PAUL · 2007 to 2022
$6.2M
Engineering CARs against cancer-specific glycoproteinsR21CA238628 · NCI · UNIVERSITY OF ILLINOIS AT URBANA-CHAMPAIGN · PI KRANZ, DAVID M. · 2019 to 2020
$394k
NCI NIH HHS R01 CA022677NCI NIH HHS R01 CA120439NCI NIH HHS R21 CA238628
6 · The paper itself

Abstract

backgroundTreatment of some blood cancers with T cells that express a chimeric antigen receptor (CAR) against CD19 have shown remarkable results. In contrast, CAR-T cell efficacy against solid tumors has been difficult to achieve.

methodsTo examine the potential of CAR-T cell treatments against ovarian cancers, we used the mouse ovarian cancer cell line ID8 in an intraperitoneal model that exhibits disseminated solid tumors in female C57BL/6J mice. The CAR contained a single-chain Fv from antibody 237 which recognizes a Tn-glycopeptide-antigen expressed by ID8 due to aberrant O-linked glycosylation in the absence of the transferase-dependent chaperone

resultsIn line with many observations about the impact of aberrant O-linked glycosylation, the ID8

conclusionThe findings support the development of affinity-optimized CAR-T cells as a potential treatment for established ovarian cancer, with the most effective CARs mediating a distinct pattern of inflammatory cytokine release in vitro. Importantly, the most potent Tn-dependent CAR-T cells showed no evidence of toxicity in tumor-bearing mice in a syngeneic, immunocompetent system.

Indexed as

Ovarian NeoplasmsReceptors, Chimeric AntigenAnimalsCytokinesFemaleHumansImmunotherapy, AdoptiveMiceMice, Inbred C57BLT-LymphocytesTumor MicroenvironmentXenograft Model Antitumor AssaysCytokinesReceptors, Chimeric AntigenAntigens, Tumor-Associated, CarbohydrateCell EngineeringImmunotherapyReceptors, Chimeric AntigenT-Lymphocytes

Identifiers

PMID37258040
PMCPMC10255004
OpenAlexW4378907890

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.