Evidence map›Paper›PMID 38979422›Full record

ArticleFrontiers in immunology2024

CXCR4 has a dual role in improving the efficacy of BCMA-redirected CAR-NK cells in multiple myeloma.

Michael W Moles, Henry Erdlei, Lutz Menzel, Marialucia Massaro, Agnese Fiori, Mario Bunse, Moritz Schrimpf, Kerstin Gerlach, Venugopal Gudipati, John Reiser and 7 more

Abstract 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. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing 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

15 citing papers in PubMed.

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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

17 authors.

Michael W Moles *Translational Tumorimmunology, Max Delbrück Center, Berlin, Germany.
Henry Erdlei *Translational Tumorimmunology, Max Delbrück Center, Berlin, Germany.
Lutz Menzel *Translational Tumorimmunology, Max Delbrück Center, Berlin, Germany.
Marialucia MassaroMicroenvironmental Regulation in Autoimmunity and Cancer, Max Delbrück Center, Berlin, Germany.
Agnese FioriTranslational Tumorimmunology, Max Delbrück Center, Berlin, Germany.
Mario BunseMicroenvironmental Regulation in Autoimmunity and Cancer, Max Delbrück Center, Berlin, Germany.
Moritz SchrimpfTranslational Tumorimmunology, Max Delbrück Center, Berlin, Germany.
Kerstin GerlachTranslational Tumorimmunology, Max Delbrück Center, Berlin, Germany.
Venugopal GudipatiCenter for Pathophysiology, Infectiology and Immunology, Institute for Hygiene and Applied Immunology, Medical University of Vienna, Vienna, Austria.
John ReiserFate Therapeutics, San Diego, CA, United States.
Ketan MathavanFate Therapeutics, San Diego, CA, United States.
Jodie P GoodrichFate Therapeutics, San Diego, CA, United States.
Johannes B HuppaCenter for Pathophysiology, Infectiology and Immunology, Institute for Hygiene and Applied Immunology, Medical University of Vienna, Vienna, Austria.
Jan KrönkeDepartment of Hematology, Oncology and Tumorimmunology, Charité-University Medicine Berlin, Berlin, Germany.
Bahram ValamehrFate Therapeutics, San Diego, CA, United States.
Uta E HöpkenMicroenvironmental Regulation in Autoimmunity and Cancer, Max Delbrück Center, Berlin, Germany.
Armin RehmTranslational Tumorimmunology, Max Delbrück Center, Berlin, Germany.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Multiple myeloma (MM) is a plasma cell disease with a preferential bone marrow (BM) tropism. Enforced expression of tissue-specific chemokine receptors has been shown to successfully guide adoptively-transferred CAR NK cells towards the malignant milieu in solid cancers, but also to BM-resident AML and MM. For redirection towards BM-associated chemokine CXCL12, we armored BCMA CAR-NK-92 as well as primary NK cells with ectopic expression of either wildtype CXCR4 or a gain-of-function mutant CXCR4

Indexed as

B-Cell Maturation AntigenChemokine CXCL12Immunotherapy, AdoptiveKiller Cells, NaturalMultiple MyelomaReceptors, Chimeric AntigenReceptors, CXCR4Cell Line, TumorCytotoxicity, ImmunologicHumansB-Cell Maturation AntigenChemokine CXCL12CXCL12 protein, humanCXCR4 protein, humanReceptors, Chimeric AntigenReceptors, CXCR4TNFRSF17 protein, humanadoptive T cell therapyBCMAchemokine receptor CXCR4chimeric antigen receptormultiple myelomaNK cells

Identifiers

PMID38979422
PMCPMC11228140

What OpenQuestion holds

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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.