Evidence map›Paper›PMID 38671086›Full record

ArticleScientific reports2024

Hyper-N-glycosylated SEL1L3 as auto-antigenic B-cell receptor target of primary vitreoretinal lymphomas.

Michelle Elbert, Frank Neumann, Maximilian Kiefer, Konstantinos Christofyllakis, Benedikt Balensiefer, Igor Kos, Gabi Carbon, Dominic Kaddu-Mulindwa, Joerg Thomas Bittenbring, Natalie Fadle and 5 more

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
0.7field-weighted citation impact, top 29% 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

4 citing papers in PubMed, 2 citations in OpenAlex.

  1. Article
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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 2 institutions in 1 country.

Michelle ElbertInternal Medicine I, Saarland University Medical Center, Homburg, Germany.
Frank NeumannInternal Medicine I, Saarland University Medical Center, Homburg, Germany.
Maximilian KieferInternal Medicine I, Saarland University Medical Center, Homburg, Germany.
Konstantinos ChristofyllakisInternal Medicine I, Saarland University Medical Center, Homburg, Germany.
Benedikt BalensieferInternal Medicine I, Saarland University Medical Center, Homburg, Germany.
Igor KosInternal Medicine I, Saarland University Medical Center, Homburg, Germany.
Gabi CarbonInternal Medicine I, Saarland University Medical Center, Homburg, Germany.
Dominic Kaddu-MulindwaInternal Medicine I, Saarland University Medical Center, Homburg, Germany.
Joerg Thomas BittenbringInternal Medicine I, Saarland University Medical Center, Homburg, Germany.
Natalie FadleInternal Medicine I, Saarland University Medical Center, Homburg, Germany.
Evi RegitzInternal Medicine I, Saarland University Medical Center, Homburg, Germany.
Falko FendInstitute of Pathology and Neuropathology and Comprehensive Cancer Center Tuebingen, Eberhard-Karls-University, Tuebingen, Germany.
Irina BonzheimInstitute of Pathology and Neuropathology and Comprehensive Cancer Center Tuebingen, Eberhard-Karls-University, Tuebingen, Germany.
Lorenz ThurnerInternal Medicine I, Saarland University Medical Center, Homburg, Germany.
Moritz BewarderInternal Medicine I, Saarland University Medical Center, Homburg, Germany. moritz.bewarder@uks.eu.
Saarland University · DEUniversity of Tübingen · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Primary vitreoretinal lymphoma (PVRL) is a rare subtype of DLBCL and can progress into primary central nervous system lymphoma (PCNSL). To investigate the role of chronic antigenic stimulation in PVRL, we cloned and expressed B-cell receptors (BCR) from PVRL patients and tested for binding against human auto-antigens. SEL1L3, a protein with multiple glycosylation sites, was identified as the BCR target in 3/20 PVRL cases. SEL1L3 induces proliferation and BCR pathway activation in aggressive lymphoma cell lines. Moreover, SEL1L3 conjugated to a toxin killed exclusively lymphoma cells with respective BCR-reactivity. Western Blot analysis indicates the occurrence of hyper-N-glycosylation of SEL1L3 at aa 527 in PVRL patients with SEL1L3-reactive BCRs. The BCR of a PVRL patient with serum antibodies against SEL1L3 was cloned from a vitreous body biopsy at diagnosis and of a systemic manifestation at relapse. VH4-04*07 was used in both lymphoma manifestations with highly conserved CDR3 regions. Both BCRs showed binding to SEL1L3, suggesting continued dependence of lymphoma cells on antigen stimulation. These results indicate an important role of antigenic stimulation by post-translationally modified auto-antigens in the genesis of PVRL. They also provide the basis for a new treatment approach targeting unique lymphoma BCRs with ultimate specificity.

Indexed as

Receptors, Antigen, B-CellAgedAutoantigensCell Line, TumorFemaleGlycosylationHumansLymphoma, Large B-Cell, DiffuseMaleMiddle AgedRetinal NeoplasmsVitreous BodyAutoantigensReceptors, Antigen, B-CellAuto-antigensB-cell receptor antigensPrimary CNS lymphomaPrimary vitreoretinal lymphomaSAMD14/neurabin-ISEL1L3

Identifiers

PMID38671086
PMCPMC11053041
OpenAlexW4395684858

What OpenQuestion holds

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LicenceCC BY
Read underepoch 390

Registered trials

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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.