Evidence map›Paper›PMID 32111817›Full record

ArticleBlood cancer journal2020

Mass spectrometry-based identification of a B-cell maturation antigen-derived T-cell epitope for antigen-specific immunotherapy of multiple myeloma.

Tatjana Bilich, Annika Nelde, Jens Bauer, Simon Walz, Malte Roerden, Helmut R Salih, Katja Weisel, Britta Besemer, Ana Marcu, Maren Lübke and 5 more

Open access · goldAbstract read
In one paragraph

Article in Blood cancer journal, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
1.2field-weighted citation impact, top 21% 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

10 citing papers in PubMed, 21 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

15 authors at 6 institutions in 2 countries.

Tatjana BilichUniversity Hospital Tübingen, Clinical Collaboration Unit Translational Immunology, German Cancer Consortium (DKTK), Tübingen, Germany.ORCID http://orcid.org/0000-0002-8107-0419
Annika NeldeUniversity Hospital Tübingen, Clinical Collaboration Unit Translational Immunology, German Cancer Consortium (DKTK), Tübingen, Germany.
Jens BauerUniversity Hospital Tübingen, Clinical Collaboration Unit Translational Immunology, German Cancer Consortium (DKTK), Tübingen, Germany.
Simon WalzUniversity of Tübingen, Institute for Cell Biology, Department of Immunology, Tübingen, Germany.
Malte RoerdenUniversity Hospital Tübingen, Department of Hematology and Oncology, Tübingen, Germany.
Helmut R SalihUniversity Hospital Tübingen, Clinical Collaboration Unit Translational Immunology, German Cancer Consortium (DKTK), Tübingen, Germany.
Katja WeiselUniversity Hospital Tübingen, Department of Hematology and Oncology, Tübingen, Germany.
Britta BesemerUniversity Hospital Tübingen, Department of Hematology and Oncology, Tübingen, Germany.
Ana MarcuUniversity of Tübingen, Institute for Cell Biology, Department of Immunology, Tübingen, Germany.
Maren LübkeUniversity of Tübingen, Institute for Cell Biology, Department of Immunology, Tübingen, Germany.
Juliane SchuhmacherUniversity of Tübingen, Institute for Cell Biology, Department of Immunology, Tübingen, Germany.
Marian C NeidertUniversity Hospital Zurich and University of Zurich, Department of Neurosurgery, Clinical Neuroscience Center, Zurich, Switzerland.
Hans-Georg RammenseeUniversity of Tübingen, Institute for Cell Biology, Department of Immunology, Tübingen, Germany.
Stefan StevanovićUniversity of Tübingen, Institute for Cell Biology, Department of Immunology, Tübingen, Germany.
Juliane S WalzUniversity Hospital Tübingen, Clinical Collaboration Unit Translational Immunology, German Cancer Consortium (DKTK), Tübingen, Germany. juliane.walz@med.uni-tuebingen.de.
Deutschen Konsortium für Translationale Krebsforschung · DEUniversity Children's Hospital Tübingen · DEUniversity of Tübingen · DEGerman Cancer Research Center · DEUniversität Hamburg · DEUniversity of Zurich · CH

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The B-cell maturation antigen (BCMA) is currently being evaluated as promising tumor-associated surface antigen for T-cell-based immunotherapy approaches, such as CAR T cells and bispecific antibodies, in multiple myeloma (MM). Cytotoxic T cells bearing BCMA-specific T-cell receptors might further allow targeting HLA-presented antigens derived from the intracellular domain of BCMA. By analyzing a mass spectrometry-acquired immunopeptidome dataset of primary MM samples and MM cell lines for BCMA-derived HLA ligands, we identified the naturally presented HLA-B*18-restricted ligand P(BCMA)

Indexed as

Antibodies, MonoclonalB-Cell Maturation AntigenCase-Control StudiesCD8-Positive T-LymphocytesEpitopes, T-LymphocyteFeasibility StudiesHealthy VolunteersHumansImmunotherapyMass SpectrometryMultiple MyelomaNeoplasm ProteinsT-Lymphocytes, CytotoxicAntibodies, MonoclonalB-Cell Maturation AntigenEpitopes, T-LymphocyteNeoplasm Proteins

Identifiers

PMID32111817
PMCPMC7048774
OpenAlexW3007462451

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.