Evidence map›Paper›PMID 39781381›Full record

ArticleFrontiers in immunology2024

Anti-Mesothelin CAR-NK cells as a novel targeted therapy against cervical cancer.

Ivana Kutle, Robert Polten, Jan Lennart Stalp, Jens Hachenberg, Felix Todzey, Ralf Hass, Katharina Zimmermann, Juliane von der Ohe, Constantin von Kaisenberg, Lavinia Neubert and 7 more

Erratum issuedAbstract read
In one paragraph

Article in Frontiers in immunology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
–field-weighted citation impact
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

19 citing papers in PubMed.

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  16. Cell-Based Therapies for Solid Tumors: Challenges and Advances.International journal of molecular sciences · 2025
    Review
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  18. NK cells in HPV-related tumorigenesis: mechanisms and clinical applications.Frontiers in cellular and infection microbiology · 2025
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

17 authors.

Ivana Kutle *Institute of Experimental Hematology, Hannover Medical School, Hannover, Germany.
Robert Polten *Institute of Experimental Hematology, Hannover Medical School, Hannover, Germany.
Jan Lennart StalpInstitute of Experimental Hematology, Hannover Medical School, Hannover, Germany.
Jens HachenbergInstitute of Experimental Hematology, Hannover Medical School, Hannover, Germany.
Felix TodzeyInstitute of Experimental Hematology, Hannover Medical School, Hannover, Germany.
Ralf HassDepartment of Gynecology and Obstetrics, Hannover Medical School, Hannover, Germany.
Katharina ZimmermannInstitute of Experimental Hematology, Hannover Medical School, Hannover, Germany.
Juliane von der OheDepartment of Gynecology and Obstetrics, Hannover Medical School, Hannover, Germany.
Constantin von KaisenbergDepartment of Gynecology and Obstetrics, Hannover Medical School, Hannover, Germany.
Lavinia NeubertInstitute of Pathology, Hannover Medical School, Hannover, Germany.
Jan C KampBiomedical Research in Endstage and Obstructive Lung Disease Hannover (BREATH), German Center for Lung Research (DZL), Hannover, Germany.
Dirk SchaudienFraunhofer Institute for Toxicology and Experimental Medicine, ITEM, Hannover, Germany.
Ann-Kathrin SeydaInstitute of Experimental Hematology, Hannover Medical School, Hannover, Germany.
Peter HillemannsDepartment of Gynecology and Obstetrics, Hannover Medical School, Hannover, Germany.
Rüdiger KlapdorInstitute of Experimental Hematology, Hannover Medical School, Hannover, Germany.
Michael Alexander MorganInstitute of Experimental Hematology, Hannover Medical School, Hannover, Germany.
Axel SchambachInstitute of Experimental Hematology, Hannover Medical School, Hannover, Germany.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Resistance to the currently available treatment paradigms is one of the main factors that contributes to poor outcomes in patients with advanced cervical cancer. Novel targeted therapy approaches might enhance the patient's treatment outcome and are urgently needed for this malignancy. While chimeric-antigen receptor (CAR)-based adoptive immunotherapy displays a promising treatment strategy for liquid cancers, their use against cervical cancer is largely unexplored. This study used alpharetroviral SIN vectors to equip natural killer (NK) cells with a third-generation CAR (including CD28 and 4-1BB co-stimulatory domains) targeting Mesothelin, which was identified to be highly expressed on primary human cervical cancer tissues and cervical cancer cell lines in this and other studies. Anti-Mesothelin CAR-NK cells demonstrated high cytotoxicity against cervical cancer cells in 2D and 3D culture models, which corresponded to increased degranulation of CAR-NK-92 cells upon exposure to Mesothelin

Indexed as

GPI-Linked ProteinsImmunotherapy, AdoptiveKiller Cells, NaturalMesothelinReceptors, Chimeric AntigenUterine Cervical NeoplasmsCell Line, TumorCytotoxicity, ImmunologicFemaleHumansGPI-Linked ProteinsMesothelinReceptors, Chimeric AntigenCAR-NK cellsCAR-T cellscervical cancerchemotherapychimeric antigen receptor (CAR)immunotherapyMesothelin

Identifiers

PMID39781381
PMCPMC11707549

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Registered trials

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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.