Evidence map›Paper›PMID 29955130›Full record

ArticleLeukemia2019

LRPAP1 is a frequent proliferation-inducing antigen of BCRs of mantle cell lymphomas and can be used for specific therapeutic targeting.

Lorenz Thurner, Sylvia Hartmann, Natalie Fadle, Maria Kemele, Theresa Bock, Moritz Bewarder, Evi Regitz, Frank Neumann, Anna Nimmesgern, Lutz von Müller and 8 more

Abstract read
PubMed Publisher
In one paragraph

Article in Leukemia, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed, 1 pooled it
2.0field-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

22 citing papers in PubMed, 1 synthesis or guideline pooled it, 25 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

18 authors at 5 institutions in 2 countries.

Lorenz ThurnerJosé Carreras Center for Immuno- and Gene Therapy and Internal Medicine I, Saarland University Medical School, Homburg/Saar, Germany. lorenz.thurner@uks.eu.
Sylvia HartmannDr. Senckenberg Institute of Pathology, Goethe University Hospital, Frankfurt am Main, Germany.
Natalie FadleJosé Carreras Center for Immuno- and Gene Therapy and Internal Medicine I, Saarland University Medical School, Homburg/Saar, Germany.
Maria KemeleJosé Carreras Center for Immuno- and Gene Therapy and Internal Medicine I, Saarland University Medical School, Homburg/Saar, Germany.
Theresa BockJosé Carreras Center for Immuno- and Gene Therapy and Internal Medicine I, Saarland University Medical School, Homburg/Saar, Germany.
Moritz BewarderJosé Carreras Center for Immuno- and Gene Therapy and Internal Medicine I, Saarland University Medical School, Homburg/Saar, Germany.
Evi RegitzJosé Carreras Center for Immuno- and Gene Therapy and Internal Medicine I, Saarland University Medical School, Homburg/Saar, Germany.
Frank NeumannJosé Carreras Center for Immuno- and Gene Therapy and Internal Medicine I, Saarland University Medical School, Homburg/Saar, Germany.
Anna NimmesgernInstitute of Medical Microbiology and Hygiene, Saarland University, Homburg/Saar, Germany.
Lutz von MüllerInstitute of Medical Microbiology and Hygiene, Saarland University, Homburg/Saar, Germany.
Christiane PottSecond Department of Medicine, University Hospital Schleswig-Holstein, Kiel, Germany.
Yoo-Jin KimSaarland University Medical School, Institute of Pathology, Homburg/Saar, Germany.
Rainer Maria BohleSaarland University Medical School, Institute of Pathology, Homburg/Saar, Germany.
Mariusz WasikLymphoma Program, Abramson Cancer Center University of Pennsylvania, Philadelphia, PA, USA.
Stephen J SchusterLymphoma Program, Abramson Cancer Center University of Pennsylvania, Philadelphia, PA, USA.
Martin-Leo HansmannDr. Senckenberg Institute of Pathology, Goethe University Hospital, Frankfurt am Main, Germany.
Klaus-Dieter PreussJosé Carreras Center for Immuno- and Gene Therapy and Internal Medicine I, Saarland University Medical School, Homburg/Saar, Germany.
Michael PfreundschuhJosé Carreras Center for Immuno- and Gene Therapy and Internal Medicine I, Saarland University Medical School, Homburg/Saar, Germany.ORCID http://orcid.org/0000-0001-6982-8218
Saarland University · DEGoethe University Frankfurt · DEInstitute of Medical Microbiology and Hygiene · DEUPMC Hillman Cancer Center · USUniversity Hospital Schleswig-Holstein · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The predominant usage of VH4-34 and V3-21 and reports of stereotyped CDR3s suggest a shared antigenic target of B-cell receptors (BCR) from mantle cell lymphomas (MCL). To identify the target antigens of MCL-BCRs, BCRs from 21 patients and seven MCL cell lines were recombinantly expressed and used for antigen screening. The BCRs from 8/21 patients and 2/7 MCL cell lines reacted specifically with the autoantigen low-density lipoprotein receptor-related protein-associated protein 1 (LRPAP1). High-titered and light chain-restricted anti-LRPAP1 serum antibodies were found in MCL patients, but not in controls. LRPAP1 induced proliferation by BCR pathway activation, while an LRPAP1-ETA' toxin-conjugate specifically killed MCL cells with LRPAP1-specific BCRs. Our results suggest a role of LRPAP1 in lymphomagenesis and maintenance of a considerable proportion of MCL cases by chronic autoantigenic stimulation, likely evolving from a chronic autoreactive B-cell response. Importantly, LRPAP1 can be used for a novel therapeutic approach that targets MCL with LRPAP1-reactive BCRs with high specificity.

Indexed as

AutoantigensB-LymphocytesCell ProliferationHumansLDL-Receptor Related Protein-Associated ProteinLymphoma, Mantle-CellReceptors, Antigen, B-CellTumor Cells, CulturedAutoantigensLDL-Receptor Related Protein-Associated ProteinReceptors, Antigen, B-Cell

Identifiers

PMID29955130
OpenAlexW2809961616

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.