Evidence map›Paper›PMID 34813501›Full record

ArticleThe Journal of clinical investigation2022

B cell receptor isotypes differentially associate with cell signaling, kinetics, and outcome in chronic lymphocytic leukemia.

Andrea N Mazzarello, Eva Gentner-Göbel, Marcus Dühren-von Minden, Tatyana N Tarasenko, Antonella Nicolò, Gerardo Ferrer, Stefano Vergani, Yun Liu, Davide Bagnara, Kanti R Rai and 5 more

Open access · hybridAbstract read
In one paragraph

Article in The Journal of clinical investigation, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
1.7field-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

13 citing papers in PubMed, 17 citations in OpenAlex.

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  8. Unexpected CD5Journal of clinical medicine · 2023
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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 4 institutions in 3 countries.

Andrea N MazzarelloKarches Center for Oncology Research, The Feinstein Institutes for Medical Research, Northwell Health, Manhasset, New York, USA.
Eva Gentner-GöbelInstitute for Immunology, University Hospital Ulm, Ulm, Germany.
Marcus Dühren-von MindenInstitute for Immunology, University Hospital Ulm, Ulm, Germany.
Tatyana N TarasenkoMetabolism, Infection and Immunity Section, National Human Genome Research Institute, NIH, Bethesda, Maryland, USA.
Antonella NicolòInstitute for Immunology, University Hospital Ulm, Ulm, Germany.
Gerardo FerrerKarches Center for Oncology Research, The Feinstein Institutes for Medical Research, Northwell Health, Manhasset, New York, USA.
Stefano VerganiKarches Center for Oncology Research, The Feinstein Institutes for Medical Research, Northwell Health, Manhasset, New York, USA.
Yun LiuKarches Center for Oncology Research, The Feinstein Institutes for Medical Research, Northwell Health, Manhasset, New York, USA.
Davide BagnaraKarches Center for Oncology Research, The Feinstein Institutes for Medical Research, Northwell Health, Manhasset, New York, USA.
Kanti R RaiKarches Center for Oncology Research, The Feinstein Institutes for Medical Research, Northwell Health, Manhasset, New York, USA.
Jan A BurgerDepartment of Leukemia, MD Anderson Cancer Center, Houston, Texas, USA.
Peter J McGuireMetabolism, Infection and Immunity Section, National Human Genome Research Institute, NIH, Bethesda, Maryland, USA.
Palash C MaityInstitute for Immunology, University Hospital Ulm, Ulm, Germany.
Hassan JumaaInstitute for Immunology, University Hospital Ulm, Ulm, Germany.
Nicholas ChiorazziKarches Center for Oncology Research, The Feinstein Institutes for Medical Research, Northwell Health, Manhasset, New York, USA.
Northwell Health · USUniversity Hospital Ulm · DENational Human Genome Research Institute · USThe University of Texas MD Anderson Cancer Center · US

Funding

European Research Council 694992
6 · The paper itself

Abstract

In chronic lymphocytic leukemia (CLL), the B cell receptor (BCR) plays a critical role in disease development and progression, as indicated by the therapeutic efficacy of drugs blocking BCR signaling. However, the mechanism(s) underlying BCR responsiveness are not completely defined. Selective engagement of membrane IgM or IgD on CLL cells, each coexpressed by more than 90% of cases, leads to distinct signaling events. Since both IgM and IgD carry the same antigen-binding domains, the divergent actions of the receptors are attributed to differences in immunoglobulin (Ig) structure or the outcome of signal transduction. We showed that IgM, not IgD, level and organization associated with CLL-cell birth rate and the type and consequences of BCR signaling in humans and mice. The latter IgM-driven effects were abrogated when BCR signaling was inhibited. Collectively, these studies demonstrated a critical, selective role for IgM in BCR signaling and B cell fate decisions, possibly opening new avenues for CLL therapy.

Indexed as

AnimalsB-LymphocytesFemaleHumansImmunoglobulin DImmunoglobulin MLeukemia, Lymphocytic, Chronic, B-CellMaleMiceMice, KnockoutReceptors, Antigen, B-CellSignal TransductionImmunoglobulin DImmunoglobulin MReceptors, Antigen, B-CellImmunoglobulinsImmunologyLeukemiasOncologySignal transduction

Identifiers

PMID34813501
PMCPMC8759784
OpenAlexW3215157384

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.