Evidence map›Paper›PMID 32536913›Full record

ArticleFrontiers in immunology2020

Analysis of the Targets and Glycosylation of Monoclonal IgAs From MGUS and Myeloma Patients.

Adrien Bosseboeuf, Célia Seillier, Nicolas Mennesson, Sophie Allain-Maillet, Maeva Fourny, Anne Tallet, Eric Piver, Philippe Lehours, Francis Mégraud, Laureline Berthelot and 3 more

Open access · goldAbstract read
In one paragraph

Article in Frontiers in immunology, 2020. 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
1.2field-weighted citation impact, top 22% 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, 15 citations in OpenAlex.

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  12. Immunoglobulin A Glycosylation and Its Role in Disease.Experientia supplementum (2012) · 2021
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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

13 authors at 6 institutions in 1 country.

Adrien BosseboeufCRCINA, Inserm, Université de Nantes, Université d'Angers, Nantes, France.
Célia SeillierCRCINA, Inserm, Université de Nantes, Université d'Angers, Nantes, France.
Nicolas MennessonCRCINA, Inserm, Université de Nantes, Université d'Angers, Nantes, France.
Sophie Allain-MailletCRCINA, Inserm, Université de Nantes, Université d'Angers, Nantes, France.
Maeva FournyCRCINA, Inserm, Université de Nantes, Université d'Angers, Nantes, France.
Anne TalletLaboratoire de Biochimie, CHU de Tours, Tours, France.
Eric PiverLaboratoire de Biochimie, CHU de Tours, Tours, France.
Philippe LehoursInserm U1053, Université de Bordeaux, Bordeaux, France.
Francis MégraudInserm U1053, Université de Bordeaux, Bordeaux, France.
Laureline BerthelotCentre de Recherche en Transplantation et Immunologie UMR1064, Inserm, Université de Nantes, Nantes, France.
Jean HarbCRCINA, Inserm, Université de Nantes, Université d'Angers, Nantes, France.
Edith Bigot-CorbelCRCINA, Inserm, Université de Nantes, Université d'Angers, Nantes, France.
Sylvie HermouetCRCINA, Inserm, Université de Nantes, Université d'Angers, Nantes, France.
Inserm · FRNantes Université · FRUniversité d'Angers · FRCentre Hospitalier Universitaire de Nantes · FRCentre Hospitalier Universitaire de Tours · FRUniversité de Bordeaux · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Previous studies showed that monoclonal immunoglobulins G (IgGs) of "monoclonal gammopathy of undetermined significance" (MGUS) and myeloma were hyposialylated, thus presumably pro-inflammatory, and for about half of patients, the target of the monoclonal IgG was either a virus-Epstein-Barr virus (EBV), other herpes viruses, hepatitis C virus (HCV)-or a glucolipid, lysoglucosylceramide (LGL1), suggesting antigen-driven disease in these patients. In the present study, we show that monoclonal IgAs share these characteristics. We collected 35 sera of patients with a monoclonal IgA (6 MGUS, 29 myeloma), and we were able to purify 25 of the 35 monoclonal IgAs (6 MGUS, 19 myeloma). Monoclonal IgAs from MGUS and myeloma patients were significantly less sialylated than IgAs from healthy volunteers. When purified monoclonal IgAs were tested against infectious pathogens and LGL1, five myeloma patients had a monoclonal IgA that specifically recognized viral proteins: the core protein of HCV in one case, EBV nuclear antigen 1 (EBNA-1) in four cases (21.1% of IgA myeloma). Monoclonal IgAs from three myeloma patients reacted against LGL1. In summary, monoclonal IgAs are hyposialylated and as described for IgG myeloma, significant subsets (8/19, or 42%) of patients with IgA myeloma may have viral or self (LGL1) antigen-driven disease.

Indexed as

AgedAged, 80 and overAntibodies, MonoclonalAntigens, ViralCohort StudiesEpstein-Barr Virus InfectionsEpstein-Barr Virus Nuclear AntigensFemaleGlucosylceramidesGlycosylationHepacivirusHepatitis CHerpesvirus 4, HumanHumansImmunoglobulin AMaleAntibodies, MonoclonalAntigens, ViralEBV-encoded nuclear antigen 1Epstein-Barr Virus Nuclear AntigensGlucosylceramidesImmunoglobulin Anucleocapsid protein, Hepatitis C virusViral Core ProteinsEpstein–Barr virushepatitis C virusinfectious antigenslysoglucosylceramide (LGL-1)monoclonal gammopathy of undetermined significance (MGUS)monoclonal immunoglobulin A (IgA)multiple myelomasialylation

Identifiers

PMID32536913
PMCPMC7266999
OpenAlexW3028865826

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.