Evidence map›Paper›PMID 28978808›Full record

ArticleJCI insight2017

Monoclonal IgG in MGUS and multiple myeloma targets infectious pathogens.

Adrien Bosseboeuf, Delphine Feron, Anne Tallet, Cédric Rossi, Cathy Charlier, Laurent Garderet, Denis Caillot, Philippe Moreau, Marina Cardó-Vila, Renata Pasqualini and 10 more

Open access · goldAbstract readMulticenter Study
In one paragraph

Article in JCI insight, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 29 papers.

0numbers the graph read from it
0cells of the map it votes in
29citing papers in PubMed
2.7field-weighted citation impact, top 9% 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

29 citing papers in PubMed, 45 citations in OpenAlex.

  1. Race-Dependent Differences in Risk, Genomics, and Epstein-Barr Virus Exposure in Monoclonal Gammopathies: Results of SWOG S0120.Clinical cancer research : an official journal of the American Association for Cancer Research · 2020
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  9. Short-Chain Fatty Acid Production by Gut Microbiota Predicts Treatment Response in Multiple Myeloma.Clinical cancer research : an official journal of the American Association for Cancer Research · 2024
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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

20 authors at 6 institutions in 3 countries.

Adrien BosseboeufCRCINA, Inserm, Université de Nantes, Nantes, France.
Delphine FeronCRCINA, Inserm, Université de Nantes, Nantes, France.
Anne TalletLaboratoire de Biochimie, CHU Tours, Tours, France.
Cédric RossiClinical Hematology, CHU Dijon, Dijon, France.
Cathy CharlierCNRS UMR6286, Fonctionnalité et Ingénierie des Protéines (UFIP), Université de Nantes, Nantes, France.
Laurent GarderetInserm, UMRS938, Paris, France.
Denis CaillotClinical Hematology, CHU Dijon, Dijon, France.
Philippe MoreauHematology Department, CHU Nantes, Nantes, France.
Marina Cardó-VilaDivision of Molecular Medicine, Department of Internal Medicine, University of New Mexico School of Medicine, Albuquerque, New Mexico, USA.
Renata PasqualiniDivision of Molecular Medicine, Department of Internal Medicine, University of New Mexico School of Medicine, Albuquerque, New Mexico, USA.
Wadih ArapUniversity of New Mexico Comprehensive Cancer Center, Albuquerque, New Mexico, USA.
Alfreda Destea NelsonUniversity of New Mexico Comprehensive Cancer Center, Albuquerque, New Mexico, USA.
Bridget S WilsonUniversity of New Mexico Comprehensive Cancer Center, Albuquerque, New Mexico, USA.
Hélène PerreaultDepartment of Chemistry, University of Manitoba, Winnipeg, Manitoba, Canada.
Eric PiverLaboratoire de Biochimie, CHU Tours, Tours, France.
Pierre WeigelCNRS UMR6286, Fonctionnalité et Ingénierie des Protéines (UFIP), Université de Nantes, Nantes, France.
François GirodonLaboratoire d'Hématologie, CHU Dijon, Dijon, France.
Jean HarbCentre de Recherche en Transplantation et Immunologie UMR1064, Inserm, Université de Nantes, Nantes, France.
Edith Bigot-CorbelCRCINA, Inserm, Université de Nantes, Nantes, France.
Sylvie HermouetCRCINA, Inserm, Université de Nantes, Nantes, France.
Inserm · FRUniversity of New Mexico · USCHU Dijon Bourgogne · FRCentre National de la Recherche Scientifique · FRCentre Hospitalier Universitaire de Tours · FRUniversity of Manitoba · CA

Funding

WOMEN'S CANCERS RESEARCH PROGRAMP30CA118100 · NCI · UNIVERSITY OF NEW MEXICO HEALTH SCIS CTR · PI Yolanda Sanchez · 2005 to 2026
$57.1M
UNM TRAININGP50GM085273 · NIGMS · UNIVERSITY OF NEW MEXICO HEALTH SCIS CTR · PI LIDKE, KEITH A · 2009 to 2018
$26.1M
FAIR Data Competency and Machine Learning Readiness for Biomedical ScientistsK12GM088021 · NIGMS · UNIVERSITY OF NEW MEXICO HEALTH SCIS CTR · PI REBECCA S. HARTLEY, Diane Lidke · 2009 to 2026
$16.4M
NCI NIH HHS P30 CA118100NIGMS NIH HHS K12 GM088021NIGMS NIH HHS P50 GM085273
6 · The paper itself

Abstract

Subsets of mature B cell neoplasms are linked to infection with intracellular pathogens such as Epstein-Barr virus (EBV), hepatitis C virus (HCV), or Helicobacter pylori. However, the association between infection and the immunoglobulin-secreting (Ig-secreting) B proliferative disorders remains largely unresolved. We investigated whether the monoclonal IgG (mc IgG) produced by patients diagnosed with monoclonal gammopathy of undetermined significance (MGUS) or multiple myeloma (MM) targets infectious pathogens. Antigen specificity of purified mc IgG from a large patient cohort (n = 244) was determined using a multiplex infectious-antigen array (MIAA), which screens for reactivity to purified antigens or lysates from 9 pathogens. Purified mc IgG from 23.4% of patients (57 of 244) specifically recognized 1 pathogen in the MIAA. EBV was the most frequent target (15.6%), with 36 of 38 mc IgGs recognizing EBV nuclear antigen-1 (EBNA-1). MM patients with EBNA-1-specific mc IgG (14.0%) showed substantially greater bone marrow plasma cell infiltration and higher β2-microglobulin and inflammation/infection-linked cytokine levels compared with other smoldering myeloma/MM patients. Five other pathogens were the targets of mc IgG: herpes virus simplex-1 (2.9%), varicella zoster virus (1.6%), cytomegalovirus (0.8%), hepatitis C virus (1.2%), and H. pylori (1.2%). We conclude that a dysregulated immune response to infection may underlie disease onset and/or progression of MGUS and MM for subsets of patients.

Indexed as

AdolescentAdultAgedAged, 80 and overAntibodies, ViralChildChild, PreschoolEpitopesEpstein-Barr Virus InfectionsEpstein-Barr Virus Nuclear AntigensFemaleHelicobacter InfectionsHelicobacter pyloriHerpes SimplexHerpesvirus 1, HumanHerpesvirus 4, HumanAntibodies, ViralEBV-encoded nuclear antigen 1EpitopesEpstein-Barr Virus Nuclear AntigensImmunoglobulin G

Identifiers

PMID28978808
PMCPMC5841870
OpenAlexW2762584070

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.