Evidence map›Paper›PMID 38641734›Full record

ArticleNature cancer2024

Single-cell multiomic dissection of response and resistance to chimeric antigen receptor T cells against BCMA in relapsed multiple myeloma.

Michael Rade, Nora Grieb, Ronald Weiss, Jaren Sia, Luise Fischer, Patrick Born, Andreas Boldt, Stephan Fricke, Paul Franz, Jonathan Scolnick and 23 more

Abstract read
PubMed Publisher
In one paragraph

Article in Nature cancer, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 48 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
48citing papers in PubMed, 1 pooled it
13.6field-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

48 citing papers in PubMed, 1 synthesis or guideline pooled it, 48 citations in OpenAlex.

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  9. Mapping clinical CAR-T cells: insights from scRNA-seq.Trends in molecular medicine · 2026
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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

33 authors at 3 institutions in 1 country.

Michael Rade *Fraunhofer Institute for Cell Therapy and Immunology IZI, Leipzig, Germany.ORCID http://orcid.org/0000-0001-6247-9289
Nora Grieb *Department of Hematology, Cellular Therapy and Hemostaseology, University Hospital of Leipzig, Leipzig, Germany.
Ronald WeissFraunhofer Institute for Cell Therapy and Immunology IZI, Leipzig, Germany.
Jaren SiaSingleron Biotechnologies, Cologne, Germany.
Luise FischerDepartment of Hematology, Cellular Therapy and Hemostaseology, University Hospital of Leipzig, Leipzig, Germany.
Patrick BornDepartment of Hematology, Cellular Therapy and Hemostaseology, University Hospital of Leipzig, Leipzig, Germany.
Andreas BoldtInstitute for Clinical Immunology, University Hospital of Leipzig, Leipzig, Germany.
Stephan FrickeInstitute for Clinical Immunology, University Hospital of Leipzig, Leipzig, Germany.
Paul FranzInstitute for Clinical Immunology, University Hospital of Leipzig, Leipzig, Germany.
Jonathan ScolnickSingleron Biotechnologies, Cologne, Germany.
Lakshmi VenkatramanSingleron Biotechnologies, Cologne, Germany.
Stacy XuSingleron Biotechnologies, Cologne, Germany.
Christina KloetzerDepartment of Hematology, Cellular Therapy and Hemostaseology, University Hospital of Leipzig, Leipzig, Germany.
Simone HeynDepartment of Hematology, Cellular Therapy and Hemostaseology, University Hospital of Leipzig, Leipzig, Germany.
Anne Sophie KubaschDepartment of Hematology, Cellular Therapy and Hemostaseology, University Hospital of Leipzig, Leipzig, Germany.
Ronny BaberInstitute for Laboratory Medicine, Clinical Chemistry and Molecular Diagnostics, University Hospital Leipzig, Leipzig, Germany.
Song Yau WangDepartment of Hematology, Cellular Therapy and Hemostaseology, University Hospital of Leipzig, Leipzig, Germany.ORCID http://orcid.org/0000-0001-5433-8750
Enrica BachDepartment of Hematology, Cellular Therapy and Hemostaseology, University Hospital of Leipzig, Leipzig, Germany.
Sandra HoffmannDepartment of Hematology, Cellular Therapy and Hemostaseology, University Hospital of Leipzig, Leipzig, Germany.
Jule UssmannDepartment of Hematology, Cellular Therapy and Hemostaseology, University Hospital of Leipzig, Leipzig, Germany.
Birthe SchetschorkeDepartment of Hematology, Cellular Therapy and Hemostaseology, University Hospital of Leipzig, Leipzig, Germany.
Saskia HellDepartment of Hematology, Cellular Therapy and Hemostaseology, University Hospital of Leipzig, Leipzig, Germany.
Sebastian SchwindDepartment of Hematology, Cellular Therapy and Hemostaseology, University Hospital of Leipzig, Leipzig, Germany.ORCID http://orcid.org/0000-0002-1315-2332
Klaus H MetzelerDepartment of Hematology, Cellular Therapy and Hemostaseology, University Hospital of Leipzig, Leipzig, Germany.
Marco HerlingDepartment of Hematology, Cellular Therapy and Hemostaseology, University Hospital of Leipzig, Leipzig, Germany.
Madlen JentzschDepartment of Hematology, Cellular Therapy and Hemostaseology, University Hospital of Leipzig, Leipzig, Germany.
Georg-Nikolaus FrankeDepartment of Hematology, Cellular Therapy and Hemostaseology, University Hospital of Leipzig, Leipzig, Germany.ORCID http://orcid.org/0000-0001-8239-002X
Ulrich SackInstitute for Clinical Immunology, University Hospital of Leipzig, Leipzig, Germany.
Ulrike KöhlFraunhofer Institute for Cell Therapy and Immunology IZI, Leipzig, Germany.
Uwe PlatzbeckerDepartment of Hematology, Cellular Therapy and Hemostaseology, University Hospital of Leipzig, Leipzig, Germany.ORCID http://orcid.org/0000-0003-1863-3239
Kristin ReicheFraunhofer Institute for Cell Therapy and Immunology IZI, Leipzig, Germany.ORCID http://orcid.org/0000-0002-4452-4872
Vladan VucinicDepartment of Hematology, Cellular Therapy and Hemostaseology, University Hospital of Leipzig, Leipzig, Germany.
Maximilian MerzDepartment of Hematology, Cellular Therapy and Hemostaseology, University Hospital of Leipzig, Leipzig, Germany. maximilian.merz@medizin.uni-leipzig.de.ORCID http://orcid.org/0000-0002-2805-5973
University Hospital Leipzig · DEFraunhofer Institute for Cell Therapy and Immunology · DEGerman Research Centre for Artificial Intelligence · DE

Funding

Deutsche Forschungsgemeinschaft (German Research Foundation) SPP microbone
6 · The paper itself

Abstract

Markers that predict response and resistance to chimeric antigen receptor (CAR) T cells in relapsed/refractory multiple myeloma are currently missing. We subjected mononuclear cells isolated from peripheral blood and bone marrow before and after the application of approved B cell maturation antigen-directed CAR T cells to single-cell multiomic analyses to identify markers associated with resistance and early relapse. Differences between responders and nonresponders were identified at the time of leukapheresis. Nonresponders showed an immunosuppressive microenvironment characterized by increased numbers of monocytes expressing the immune checkpoint molecule CD39 and suppressed CD8

Indexed as

B-Cell Maturation AntigenImmunotherapy, AdoptiveMultiple MyelomaReceptors, Chimeric AntigenAgedCD8-Positive T-LymphocytesDrug Resistance, NeoplasmFemaleHumansKiller Cells, NaturalMaleMiddle AgedNeoplasm Recurrence, LocalSingle-Cell AnalysisTumor MicroenvironmentB-Cell Maturation AntigenReceptors, Chimeric AntigenTNFRSF17 protein, human

Identifiers

PMID38641734
OpenAlexW4394955462

What OpenQuestion holds

Textmetadata
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.