Evidence map›Paper›PMID 32744145›Full record

ArticlemAbs

Novel chimerized IgA CD20 antibodies: Improving neutrophil activation against CD20-positive malignancies.

Mitchell Evers, Toine Ten Broeke, J H Marco Jansen, Maaike Nederend, Firas Hamdan, Karli R Reiding, Saskia Meyer, Petra Moerer, Iris Brinkman, Thies Rösner and 3 more

Open access · goldAbstract readVideo-Audio Media
In one paragraph

Article in mAbs. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
1.6field-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

19 citing papers in PubMed, 20 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Review
  5. Activated neutrophils: A next generation cellular immunotherapy.Bioengineering & translational medicine · 2025
    Review
  6. Review
  7. Review
  8. Article
  9. Article
  10. Article
  11. Cancer immunotherapies: A hope for the uncurable?Frontiers in molecular medicine · 2023
    Review
  12. Review
  13. Article
  14. Review
  15. Article
  16. Article
  17. Review
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  19. 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

13 authors at 5 institutions in 4 countries.

Mitchell EversCenter for Translational Immunology, University Medical Center Utrecht , Utrecht, The Netherlands.
Toine Ten BroekeDepartment of Pathology, University Medical Center Utrecht , Utrecht, The Netherlands.
J H Marco JansenCenter for Translational Immunology, University Medical Center Utrecht , Utrecht, The Netherlands.
Maaike NederendCenter for Translational Immunology, University Medical Center Utrecht , Utrecht, The Netherlands.
Firas HamdanDrug Research Program ImmunoViroTherapy Lab (IVT), University of Helsinki , Helsinki, Finland.
Karli R ReidingBiomolecular Mass Spectrometry and Proteomics, Bijvoet Center for Biomolecular Research and Utrecht Institute for Biopharmaceutical Sciences, University of Utrecht , Utrecht, The Netherlands.
Saskia MeyerDepartment of Cancer Immunology, Institute for Cancer Research, Oslo University Hospital , Oslo, Norway.
Petra MoererCenter for Translational Immunology, University Medical Center Utrecht , Utrecht, The Netherlands.
Iris BrinkmanCenter for Translational Immunology, University Medical Center Utrecht , Utrecht, The Netherlands.
Thies RösnerSection for Stem Cell Transplantation and Immunotherapy, Department of Medicine II, Christian Albrechts University and University Hospital Schleswig-Holstein , Kiel, Germany.
Robert Jan LebbinkDepartment of Medical Microbiology, University Medical Center Utrecht , CX Utrecht, The Netherlands.ORCID 0000-0002-1981-0420
Thomas ValeriusSection for Stem Cell Transplantation and Immunotherapy, Department of Medicine II, Christian Albrechts University and University Hospital Schleswig-Holstein , Kiel, Germany.
Jeanette H W LeusenCenter for Translational Immunology, University Medical Center Utrecht , Utrecht, The Netherlands.ORCID 0000-0003-4982-6914
University Medical Center Utrecht · NLChristian-Albrechts-Universität zu Kiel · DEOslo University Hospital · NOUniversity of Helsinki · FIUtrecht University · NL

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Current combination therapies elicit high response rates in B cell malignancies, often using CD20 antibodies as the backbone of therapy. However, many patients eventually relapse or develop progressive disease. Therefore, novel CD20 antibodies combining multiple effector mechanisms were generated. To study whether neutrophil-mediated destruction of B cell malignancies can be added to the arsenal of effector mechanisms, we chimerized a panel of five previously described murine CD20 antibodies to the human IgG1, IgA1 and IgA2 isotype. Of this panel, we assessed

Indexed as

Antibody-Dependent Cell CytotoxicityAnimalsAntigens, CD20B-LymphocytesHematologic NeoplasmsHumansImmunoglobulin AMiceMice, TransgenicNeoplasm ProteinsNeoplasms, ExperimentalNeutrophil ActivationNeutrophilsXenograft Model Antitumor AssaysAntigens, CD20Immunoglobulin ANeoplasm ProteinsADCCantibodiesapoptosisCD20CDCIgA

Identifiers

PMID32744145
PMCPMC7531568
OpenAlexW3046764433

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.