Evidence map›Paper›PMID 23296468›Full record

ArticleThe Journal of experimental medicine2013

A mutated B cell chronic lymphocytic leukemia subset that recognizes and responds to fungi.

Robbert Hoogeboom, Kok P M van Kessel, Frans Hochstenbach, Thera A Wormhoudt, Roy J A Reinten, Koen Wagner, Arnon P Kater, Jeroen E J Guikema, Richard J Bende, Carel J M van Noesel

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of experimental medicine, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 87 papers.

0numbers the graph read from it
0cells of the map it votes in
87citing papers in PubMed
11.2field-weighted citation impact, top 1% 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

87 citing papers in PubMed, 155 citations in OpenAlex.

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  18. Unexpected CD5Journal of clinical medicine · 2023
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27 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

10 authors at 5 institutions in 2 countries.

Robbert HoogeboomDepartment of Pathology, Academic Medical Center, University of Amsterdam, 1012 ZA Amsterdam, The Netherlands.
Kok P M van Kessel
Frans Hochstenbach
Thera A Wormhoudt
Roy J A Reinten
Koen Wagner
Arnon P Kater
Jeroen E J Guikema
Richard J Bende
Carel J M van Noesel
Pediatrics and Genetics · USAcademic Medical Center · NLAIMM Therapeutics (Netherlands) · NLUniversity of Amsterdam · NLUtrecht University · NL

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

B cell chronic lymphocytic leukemia (CLL), the most common leukemia in adults, is a clonal expansion of CD5(+)CD19(+) B lymphocytes. Two types of CLLs are being distinguished as carrying either unmutated or somatically mutated immunoglobulins (Igs), which are associated with unfavorable and favorable prognoses, respectively. More than 30% of CLLs can be grouped based on their expression of stereotypic B cell receptors (BCRs), strongly suggesting that distinctive antigens are involved in the development of CLL. Unmutated CLLs, carrying Ig heavy chain variable (IGHV) genes in germline configuration, express low-affinity, poly-, and self-reactive BCRs. However, the antigenic specificity of CLLs with mutated IGHV-genes (M-CLL) remained elusive. In this study, we describe a new subset of M-CLL, expressing stereotypic BCRs highly specific for β-(1,6)-glucan, a major antigenic determinant of yeasts and filamentous fungi. β-(1,6)-glucan binding depended on both the stereotypic Ig heavy and light chains, as well as on a distinct amino acid in the IGHV-CDR3. Reversion of IGHV mutations to germline configuration reduced the affinity for β-(1,6)-glucan, indicating that these BCRs are indeed affinity-selected for their cognate antigen. Moreover, CLL cells expressing these stereotypic receptors proliferate in response to β-(1,6)-glucan. This study establishes a class of common pathogens as functional ligands for a subset of somatically mutated human B cell lymphomas.

Indexed as

Aspergillusbeta-GlucansB-LymphocytesCandidaCase-Control StudiesCell ProliferationEpitopesHumansImmunoglobulin Heavy ChainsImmunoglobulin MImmunoglobulin Variable RegionLeukemia, Lymphocytic, Chronic, B-CellMutationReceptors, Antigen, B-CellRecombinant ProteinsSaccharomycesbeta-1,6-glucanbeta-GlucansEpitopesImmunoglobulin Heavy ChainsImmunoglobulin MImmunoglobulin Variable RegionReceptors, Antigen, B-CellRecombinant Proteins

Identifiers

PMID23296468
PMCPMC3549718
OpenAlexW2132968206

What OpenQuestion holds

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LicenceCC BY-NC-SA
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.