Evidence map›Paper›PMID 34777918›Full record

ArticleOncoimmunology2021

CS1-specific single-domain antibodies labeled with Actinium-225 prolong survival and increase CD8+ T cells and PD-L1 expression in Multiple Myeloma.

Kim De Veirman, Janik Puttemans, Ahmet Krasniqi, Thomas Ertveldt, Heleen Hanssens, Ema Romao, Dirk Hose, Cleo Goyvaert, Philip Vlummens, Serge Muyldermans and 5 more

Open access · goldAbstract read
In one paragraph

Article in Oncoimmunology, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
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

16 citing papers in PubMed, 20 citations in OpenAlex.

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  9. Frontiers in immunology · 2024
    Article
  10. Article
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  13. Article
  14. Single-Domain Antibody Theranostics on the Horizon.Journal of nuclear medicine : official publication, Society of Nuclear Medicine · 2022
    Article
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  16. Review
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 2 institutions in 2 countries.

Kim De VeirmanDepartment of Hematology and Immunology, Vrije Universiteit Brussel, Brussels, Belgium.
Janik PuttemansDepartment of Medical Imaging, Laboratory for in Vivo Cellular and Molecular Imaging, Vrije Universiteit Brussel, Brussels, Belgium.
Ahmet KrasniqiDepartment of Medical Imaging, Laboratory for in Vivo Cellular and Molecular Imaging, Vrije Universiteit Brussel, Brussels, Belgium.
Thomas ErtveldtLaboratory for Molecular and Cellular Therapy, Vrije Universiteit Brussel, Brussels, Belgium.
Heleen HanssensDepartment of Medical Imaging, Laboratory for in Vivo Cellular and Molecular Imaging, Vrije Universiteit Brussel, Brussels, Belgium.
Ema RomaoDepartment of Cellular and Molecular Immunology, Vrije Universiteit Brussel, Brussels, Belgium.
Dirk HoseDepartment of Hematology and Immunology, Vrije Universiteit Brussel, Brussels, Belgium.
Cleo GoyvaertLaboratory for Molecular and Cellular Therapy, Vrije Universiteit Brussel, Brussels, Belgium.
Philip VlummensDepartment of Hematology and Immunology, Vrije Universiteit Brussel, Brussels, Belgium.ORCID 0000-0001-8275-2887
Serge MuyldermansDepartment of Cellular and Molecular Immunology, Vrije Universiteit Brussel, Brussels, Belgium.
Karine BreckpotLaboratory for Molecular and Cellular Therapy, Vrije Universiteit Brussel, Brussels, Belgium.
Frank BruchertseiferEuropean Commission, Joint Research Centre (JRC), Karlsruhe, Germany.
Alfred MorgensternEuropean Commission, Joint Research Centre (JRC), Karlsruhe, Germany.
Matthias D'HuyvetterDepartment of Medical Imaging, Laboratory for in Vivo Cellular and Molecular Imaging, Vrije Universiteit Brussel, Brussels, Belgium.
Nick DevoogdtDepartment of Medical Imaging, Laboratory for in Vivo Cellular and Molecular Imaging, Vrije Universiteit Brussel, Brussels, Belgium.
Vrije Universiteit Brussel · BEJoint Research Centre · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Multiple myeloma (MM) is a hematological malignancy characterized by the presence of clonal plasma cells in the bone marrow niche. Despite significant therapeutic advances, MM remains incurable for the majority of patients. Targeted radionuclide therapy (TRNT) has emerged as a promising treatment option to eradicate residual cancer cells. In this study, we developed and characterized single-domain antibodies (sdAbs) against the MM-antigen CS1 and evaluated its therapeutic potential in MM using TRNT. We first validated CS1 as potential target for TRNT. CS1 is expressed in normal and malignant plasma cells in different disease stages including progression and relapse. It is expressed in dormant as well as proliferating MM cells, while low expression could be observed in environmental cells. Biodistribution studies demonstrated the specific uptake of anti-CS1 sdAbs in tissues of 5TMM cell infiltration including bone, spleen and liver. TRNT using anti-CS1 sdAbs labeled with actinium-225 significantly prolonged survival of syngeneic, immunocompetent 5T33MM mice. In addition, we observed an increase in CD8

Indexed as

Multiple MyelomaSingle-Domain AntibodiesActiniumAnimalsB7-H1 AntigenCD8-Positive T-LymphocytesHumansMiceSignaling Lymphocytic Activation Molecule FamilyTissue DistributionXenograft Model Antitumor AssaysActiniumActinium-225B7-H1 AntigenSignaling Lymphocytic Activation Molecule FamilySingle-Domain AntibodiesCS1Multiple Myelomasingle domain antibodytargeted radionuclide therapy

Identifiers

PMID34777918
PMCPMC8583167
OpenAlexW3213146675

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.