Evidence map›Paper›PMID 25953704›Full record

ArticleMolecular oncology2015

Potent anti-tumor response by targeting B cell maturation antigen (BCMA) in a mouse model of multiple myeloma.

Felix Oden, Stephen F Marino, Janko Brand, Susanne Scheu, Cathleen Kriegel, Daniel Olal, Anna Takvorian, Jörg Westermann, Buket Yilmaz, Michael Hinz and 4 more

Open access · bronzeAbstract read
In one paragraph

Article in Molecular oncology, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed, 1 pooled it
1.9field-weighted citation impact, top 14% 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

22 citing papers in PubMed, 1 synthesis or guideline pooled it, 34 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Structure-based humanization of a therapeutic antibody for multiple myeloma.Journal of molecular medicine (Berlin, Germany) · 2024
    Article
  4. Article
  5. Article
  6. Article
  7. EBAG9 silencing exerts an immune checkpoint function without aggravating adverse effects.Molecular therapy : the journal of the American Society of Gene Therapy · 2022
    Article
  8. Article
  9. Comparison of FACS and PCR for Detection of BCMA-CAR-T Cells.International journal of molecular sciences · 2022
    Article
  10. Article
  11. Review
  12. Article
  13. An Anti-BCMA RNA Aptamer for miRNA Intracellular Delivery.Molecular therapy. Nucleic acids · 2019
    Article
  14. Preclinical Evaluation of Allogeneic CAR T Cells Targeting BCMA for the Treatment of Multiple Myeloma.Molecular therapy : the journal of the American Society of Gene Therapy · 2019
    Article
  15. Prognostic Significance of Serum BAFF, APRIL, TACI and BCMA Levels in Chronic Lymphocytic Leukemia.Indian journal of hematology & blood transfusion : an official journal of Indian Society of Hematology and Blood Transfusion · 2019
    Article
  16. Review
  17. Article
  18. Article
  19. Review
  20. Article
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

14 authors at 2 institutions in 1 country.

Felix OdenMax-Delbrück-Center of Molecular Medicine (MDC), Department of Tumor Genetics and Immunogenetics, Robert-Rössle-Strasse 10, 13125 Berlin, Germany. Electronic address: felix.oden@mdc-berlin.de.
Stephen F MarinoMax-Delbrück-Center of Molecular Medicine, Crystallography, Robert-Rössle-Strasse 10, 13125 Berlin, Germany. Electronic address: stephen.marino@mdc-berlin.de.
Janko BrandMax-Delbrück-Center of Molecular Medicine, Crystallography, Robert-Rössle-Strasse 10, 13125 Berlin, Germany.
Susanne ScheuMax-Delbrück-Center of Molecular Medicine (MDC), Department of Tumor Genetics and Immunogenetics, Robert-Rössle-Strasse 10, 13125 Berlin, Germany.
Cathleen KriegelMax-Delbrück-Center of Molecular Medicine (MDC), Department of Tumor Genetics and Immunogenetics, Robert-Rössle-Strasse 10, 13125 Berlin, Germany.
Daniel OlalMax-Delbrück-Center of Molecular Medicine, Crystallography, Robert-Rössle-Strasse 10, 13125 Berlin, Germany.
Anna TakvorianCharité University Medicine Berlin, Campus Virchow-Klinikum, Department of Hematology, Oncology and Tumor Immunology, Augustenburger Platz 1, 13353 Berlin, Germany.
Jörg WestermannCharité University Medicine Berlin, Campus Virchow-Klinikum, Department of Hematology, Oncology and Tumor Immunology, Augustenburger Platz 1, 13353 Berlin, Germany.
Buket YilmazMax-Delbrück-Center for Molecular Medicine (MDC), Department of Signal Transduction in Tumor Cells, Robert-Rössle-Strasse 10, 13125 Berlin, Germany.
Michael HinzMax-Delbrück-Center for Molecular Medicine (MDC), Department of Signal Transduction in Tumor Cells, Robert-Rössle-Strasse 10, 13125 Berlin, Germany.
Oliver DaumkeMax-Delbrück-Center of Molecular Medicine, Crystallography, Robert-Rössle-Strasse 10, 13125 Berlin, Germany.
Uta E HöpkenMax-Delbrück-Center of Molecular Medicine (MDC), Department of Tumor Genetics and Immunogenetics, Robert-Rössle-Strasse 10, 13125 Berlin, Germany.
Gerd MüllerMax-Delbrück-Center of Molecular Medicine (MDC), Department of Tumor Genetics and Immunogenetics, Robert-Rössle-Strasse 10, 13125 Berlin, Germany.
Martin LippMax-Delbrück-Center of Molecular Medicine (MDC), Department of Tumor Genetics and Immunogenetics, Robert-Rössle-Strasse 10, 13125 Berlin, Germany. Electronic address: mlipp@mdc-berlin.de.
Max Delbrück Center · DECharité - Universitätsmedizin Berlin · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Multiple myeloma (MM) is an aggressive incurable plasma cell malignancy with a median life expectancy of less than seven years. Antibody-based therapies have demonstrated substantial clinical benefit for patients with hematological malignancies, particular in B cell Non-Hodgkin's lymphoma. The lack of immunotherapies specifically targeting MM cells led us to develop a human-mouse chimeric antibody directed against the B cell maturation antigen (BCMA), which is almost exclusively expressed on plasma cells and multiple myeloma cells. The high affinity antibody blocks the binding of the native ligands APRIL and BAFF to BCMA. This finding is rationalized by the high resolution crystal structure of the Fab fragment in complex with the extracellular domain of BCMA. Most importantly, the antibody effectively depletes MM cells in vitro and in vivo and substantially prolongs tumor-free survival under therapeutic conditions in a xenograft mouse model. A BCMA-antibody-based therapy is therefore a promising option for the effective treatment of multiple myeloma and autoimmune diseases.

Indexed as

AnimalsAntibody AffinityB-Cell Maturation AntigenDisease Models, AnimalEpitopesFemaleGlycosylationMiceMice, Inbred NODMice, SCIDMultiple MyelomaNF-kappa BB-Cell Maturation AntigenEpitopesNF-kappa BTnfrsf17 protein, mouseB cell maturation antigen (BCMA)High resolution X-ray structureImmunotherapyMonoclonal antibodyMultiple myelomaXenograft mouse model

Identifiers

PMID25953704
PMCPMC5528805
OpenAlexW2078044078

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.