Evidence map›Paper›PMID 38512136›Full record

ArticleThe Journal of experimental medicine2024

Antigen-independent, autonomous B cell receptor signaling drives activated B cell DLBCL.

Janneke A Eken, Marvyn T Koning, Kristyna Kupcova, Julieta H Sepúlveda Yáñez, Ruben A L de Groen, Edwin Quinten, Jurriaan Janssen, Cornelis A M van Bergen, Joost S P Vermaat, Arjen Cleven and 6 more

Open access · hybridAbstract read
In one paragraph

Article in The Journal of experimental medicine, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
7.0field-weighted citation impact, top 3% 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

14 citing papers in PubMed, 17 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

16 authors at 5 institutions in 4 countries.

Janneke A Eken *Department of Hematology, Leiden University Medical Center, Leiden, Netherlands.ORCID 0009-0004-7015-9751
Marvyn T Koning *Department of Hematology, Leiden University Medical Center, Leiden, Netherlands.ORCID 0000-0002-6993-4616
Kristyna KupcovaBIOCEV, First Faculty of Medicine, Charles University , Prague, Czech Republic.ORCID 0000-0002-4913-9877
Julieta H Sepúlveda YáñezDepartment of Hematology, Leiden University Medical Center, Leiden, Netherlands.ORCID 0000-0001-6354-3609
Ruben A L de GroenDepartment of Hematology, Leiden University Medical Center, Leiden, Netherlands.ORCID 0000-0002-2998-2066
Edwin QuintenDepartment of Hematology, Leiden University Medical Center, Leiden, Netherlands.ORCID 0000-0001-9470-9683
Jurriaan JanssenDepartment of Pathology, Amsterdam University Medical Center, Amsterdam, Netherlands.ORCID 0000-0003-2536-7864
Cornelis A M van BergenDepartment of Hematology, Leiden University Medical Center, Leiden, Netherlands.ORCID 0000-0001-6386-4517
Joost S P VermaatDepartment of Hematology, Leiden University Medical Center, Leiden, Netherlands.ORCID 0000-0002-1628-6256
Arjen ClevenDepartment of Pathology, Leiden University Medical Center, Leiden, Netherlands.ORCID 0000-0002-3672-4348
Marcelo A NavarreteSchool of Medicine, Universidad de Magallanes , Punta Arenas, Chile.ORCID 0000-0002-2044-9548
Bauke YlstraDepartment of Pathology, Amsterdam University Medical Center, Amsterdam, Netherlands.ORCID 0000-0001-9479-3010
Daphne de JongDepartment of Pathology, Amsterdam University Medical Center, Amsterdam, Netherlands.ORCID 0000-0002-9725-4060
Ondrej HavranekBIOCEV, First Faculty of Medicine, Charles University , Prague, Czech Republic.ORCID 0000-0001-5826-3557
Hassan JumaaInstitute of Immunology, University of Ulm , Ulm, Germany.ORCID 0000-0003-3383-141X
Hendrik VeelkenDepartment of Hematology, Leiden University Medical Center, Leiden, Netherlands.ORCID 0000-0002-9108-3125
Leiden University Medical Center · NLAmsterdam University Medical Centers · NLCharles University · CZUniversidad de Magallanes · CLUniversität Ulm · DE

Funding

Agencia Nacional de Investigacion y DesarrolloCharles University in Prague PRIMUS/17/MED/9Czech Health Research Council AZV NV18-03-00117Doctorado Becas Chile 2016-72170683European UnionKWF Dutch Cancer Society 10208National Institute for Cancer Research LX22NPO5102
6 · The paper itself

Abstract

Diffuse large B cell lymphoma of activated B cell type (ABC-DLBCL), a major cell-of-origin DLBCL subtype, is characterized by chronic active B cell receptor (BCR) signaling and NF-κB activation, which can be explained by activating mutations of the BCR signaling cascade in a minority of cases. We demonstrate that autonomous BCR signaling, akin to its essential pathogenetic role in chronic lymphocytic leukemia (CLL), can explain chronic active BCR signaling in ABC-DLBCL. 13 of 18 tested DLBCL-derived BCR, including 12 cases selected for expression of IgM, induced spontaneous calcium flux and increased phosphorylation of the BCR signaling cascade in murine triple knockout pre-B cells without antigenic stimulation or external BCR crosslinking. Autonomous BCR signaling was associated with IgM isotype, dependent on somatic BCR mutations and individual HCDR3 sequences, and largely restricted to non-GCB DLBCL. Autonomous BCR signaling represents a novel immunological oncogenic driver mechanism in DLBCL originating from individual BCR sequences and adds a new dimension to currently proposed genetics- and transcriptomics-based DLBCL classifications.

Indexed as

Leukemia, Lymphocytic, Chronic, B-CellLymphoma, Large B-Cell, DiffuseAnimalsB-LymphocytesImmunoglobulin MMiceReceptors, Antigen, B-CellImmunoglobulin MReceptors, Antigen, B-Cell

Identifiers

PMID38512136
PMCPMC10959178
OpenAlexW4393053919

What Socratic 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 Socratic graph.