Evidence map›Paper›PMID 22660187›Full record

ArticleLeukemia2013

The novel tribody [(CD20)(2)xCD16] efficiently triggers effector cell-mediated lysis of malignant B cells.

P Glorius, A Baerenwaldt, C Kellner, M Staudinger, M Dechant, M Stauch, F J Beurskens, P W H I Parren, J G J van de Winkel, T Valerius and 5 more

Abstract read
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Article in Leukemia, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 31 papers.

0numbers the graph read from it
0cells of the map it votes in
31citing papers in PubMed
2.5field-weighted citation impact, top 12% 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

31 citing papers in PubMed, 55 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 5 institutions in 3 countries.

P GloriusDivision of Stem Cell Transplantation and Immunotherapy, 2nd Department of Medicine, Christian-Albrechts University, Kiel, Germany.
A Baerenwaldt
C Kellner
M Staudinger
M Dechant
M Stauch
F J Beurskens
P W H I Parren
J G J van de Winkel
T Valerius
A Humpe
R Repp
M Gramatzki
F Nimmerjahn
M Peipp
Kiel University · DEFriedrich-Alexander-Universität Erlangen-Nürnberg · DEGenmab (Netherlands) · NLGenmab (United States) · USUtrecht University · NL

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Bispecific antibodies (bsab) offer a promising approach for optimizing antibody-based therapies. In the present study, [(CD20)(2)xCD16], a recombinant CD20- and CD16-directed bsab in the tribody format, was designed to optimize recruitment of FcγRIII (CD16)-positive effector cells. [(CD20)(2)xCD16] retained the antigen specificities of the parental monoclonal antibodies and binding to FcγRIIIa was not compromised by the F/V polymorphism at amino-acid position 158. [(CD20)(2)xCD16] mediated potent lysis of lymphoma cell lines and freshly isolated tumor cells from patients, even at low picomolar concentrations (∼10 pM). Irrespective of the CD16a allotype, potency as well as efficacy of lysis obtained with the tribody was significantly higher than lysis triggered by rituximab. Tumor cell killing also occurred when autologous NK cells were used as effector cells. Compared with rituximab, the tribody demonstrated depletion of autologous B cells in ex vivo whole blood assays at 100-fold lower antibody concentration. In mice with a reconstituted humanized hematopoietic system, established by transplantation of human CD34-positive cord blood cells, this novel tribody significantly depleted autologous human B cells. Thus, tribodies such as [(CD20)(2)xCD16], recruiting CD16-positive effector cells, may represent promising candidates for clinical development.

Indexed as

Antibody-Dependent Cell CytotoxicityAdultAgedAged, 80 and overAnimalsAnimals, NewbornAntibodies, BispecificAntibody SpecificityAntigens, CD20FemaleFetal BloodHumansKiller Cells, NaturalLeukemia, B-CellLymphocyte DepletionLymphoma, B-CellAntibodies, BispecificAntigens, CD20FCGR3A protein, humanReceptors, IgG

Identifiers

PMID22660187
OpenAlexW2056019889

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.