Evidence map›Paper›PMID 30510245›Full record

ArticleNature communications2018

Microbiota-driven interleukin-17-producing cells and eosinophils synergize to accelerate multiple myeloma progression.

Arianna Calcinotto, Arianna Brevi, Marta Chesi, Roberto Ferrarese, Laura Garcia Perez, Matteo Grioni, Shaji Kumar, Victoria M Garbitt, Meaghen E Sharik, Kimberly J Henderson and 10 more

Open access · goldAbstract read
In one paragraph

Article in Nature communications, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 154 papers.

0numbers the graph read from it
0cells of the map it votes in
154citing papers in PubMed
7.6field-weighted citation impact, top 2% 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

154 citing papers in PubMed, 214 citations in OpenAlex.

  1. Trial
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  15. Behçet-like Syndromes: A Comprehensive Review.Dermatopathology (Basel, Switzerland) · 2026
    Review
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  18. Article
  19. COPD-Lung Cancer Comorbidity: Mechanistic Insights and Precision Oncology Implications.International journal of chronic obstructive pulmonary disease · 2026
    Review
  20. Article

94 more citing papers are in PubMed but not listed here.

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 9 institutions in 5 countries.

Arianna CalcinottoDivision of Immunology, Transplantation and Infectious Diseases, IRCCS San Raffaele Scientific Institute, Milan, 20132, Italy.
Arianna BreviDivision of Immunology, Transplantation and Infectious Diseases, IRCCS San Raffaele Scientific Institute, Milan, 20132, Italy.
Marta ChesiComprehensive Cancer Center, Mayo Clinic Arizona, Scottsdale, AZ, 85259, USA.ORCID http://orcid.org/0000-0002-4024-8225
Roberto FerrareseLaboratory of Microbiology, IRCCS San Raffaele Scientific Institute, Milan, 20132, Italy.
Laura Garcia PerezMolekulare Immunologie und Gastroenterologie, Universitätsklinikum Hamburg-Eppendorf, Hamburg, 20246, Germany.
Matteo GrioniDivision of Immunology, Transplantation and Infectious Diseases, IRCCS San Raffaele Scientific Institute, Milan, 20132, Italy.
Shaji KumarDivision of Hematology, Mayo Clinic Rochester, Rochester, MN, 55905, USA.ORCID http://orcid.org/0000-0001-5392-9284
Victoria M GarbittComprehensive Cancer Center, Mayo Clinic Arizona, Scottsdale, AZ, 85259, USA.
Meaghen E SharikComprehensive Cancer Center, Mayo Clinic Arizona, Scottsdale, AZ, 85259, USA.
Kimberly J HendersonDivision of Hematology, Mayo Clinic Rochester, Rochester, MN, 55905, USA.
Giovanni TononDivision of Molecular Oncology, IRCCS San Raffaele Scientific Institute, Milan, 20132, Italy.
Michio TomuraFaculty of Pharmacy, Osaka Ohtani University, Osaka, 584-8540, Japan.
Yoshihiro MiwaUniversity of Tsukuba, Tsukuba, 305-8575, Japan.
Enric EspluguesDepartment of Immunobiology, School of Medicine, and Howard Hughes Medical Institute Yale University, New Haven, 06520, USA.
Richard A FlavellDepartment of Immunobiology, School of Medicine, and Howard Hughes Medical Institute Yale University, New Haven, 06520, USA.ORCID http://orcid.org/0000-0003-4461-0778
Samuel HuberMolekulare Immunologie und Gastroenterologie, Universitätsklinikum Hamburg-Eppendorf, Hamburg, 20246, Germany.
Filippo CanducciLaboratory of Microbiology, IRCCS San Raffaele Scientific Institute, Milan, 20132, Italy.ORCID http://orcid.org/0000-0002-5637-6205
Vincent S RajkumarDivision of Hematology, Mayo Clinic Rochester, Rochester, MN, 55905, USA.
P Leif BergsagelComprehensive Cancer Center, Mayo Clinic Arizona, Scottsdale, AZ, 85259, USA.ORCID http://orcid.org/0000-0003-1523-7388
Matteo BelloneDivision of Immunology, Transplantation and Infectious Diseases, IRCCS San Raffaele Scientific Institute, Milan, 20132, Italy. bellone.matteo@hsr.it.ORCID http://orcid.org/0000-0002-2586-2569
Vita-Salute San Raffaele University · ITMayo Clinic in Arizona · USMayo Clinic · USHoward Hughes Medical Institute · USUniversität Hamburg · DEIstituti di Ricovero e Cura a Carattere Scientifico · ITOsaka Ohtani University · JPUniversity of Insubria · ITUniversity of Tsukuba · JP

Funding

Project 4: Targeting Resistance to T-Cell Directed Therapy in Multiple MyelomaP50CA186781 · NCI · MAYO CLINIC ARIZONA · PI Peter Leif Bergsagel · 2015 to 2026
$25.5M
Project 3 - Modeling Proteasome Inhibitor Response and Resistance in Cell Lines and Patient Samples with Single Cell Analysis of SubpopulationsU54CA224018 · NCI · MAYO CLINIC ARIZONA · PI BERGSAGEL, PETER LEIF · 2017 to 2021
$6.0M
Onset and biomarkers for progression of monoclonal gammopathiesR01CA168762 · NCI · MAYO CLINIC ROCHESTER · PI KUMAR, SHAJI KUNNATHU, RAJKUMAR, S VINCENT · 2012 to 2024
$3.2M
Mutations that Distinguish Benign from Malignant Plasma Cell NeoplasamsR01CA195688 · NCI · MAYO CLINIC ARIZONA · PI BERGSAGEL, PETER LEIF · 2016 to 2020
$1.9M
Credentialing a Genetically Engineered Clinically-Relevant Mouse Model of Multiple MyelomaR01CA234181 · NCI · MAYO CLINIC ARIZONA · PI CHESI, MARTA · 2019 to 2023
$1.9M
PQD2 Rational Combination of Standard Agents and Immunotherapy to Treat MyelomaR01CA190045 · NCI · MAYO CLINIC ARIZONA · PI CHESI, MARTA · 2014 to 2017
$1.4M
NCI NIH HHS P50 CA186781NCI NIH HHS R01 CA168762NCI NIH HHS R01 CA190045NCI NIH HHS R01 CA195688NCI NIH HHS R01 CA234181
6 · The paper itself

Abstract

The gut microbiota has been causally linked to cancer, yet how intestinal microbes influence progression of extramucosal tumors is poorly understood. Here we provide evidence implying that Prevotella heparinolytica promotes the differentiation of Th17 cells colonizing the gut and migrating to the bone marrow (BM) of transgenic Vk*MYC mice, where they favor progression of multiple myeloma (MM). Lack of IL-17 in Vk*MYC mice, or disturbance of their microbiome delayed MM appearance. Similarly, in smoldering MM patients, higher levels of BM IL-17 predicted faster disease progression. IL-17 induced STAT3 phosphorylation in murine plasma cells, and activated eosinophils. Treatment of Vk*MYC mice with antibodies blocking IL-17, IL-17RA, and IL-5 reduced BM accumulation of Th17 cells and eosinophils and delayed disease progression. Thus, in Vk*MYC mice, commensal bacteria appear to unleash a paracrine signaling network between adaptive and innate immunity that accelerates progression to MM, and can be targeted by already available therapies.

Indexed as

AnimalsBone MarrowCell DifferentiationCell MovementDisease ProgressionEosinophilsGastrointestinal MicrobiomeHumansInterleukin-17Mice, Inbred C57BLMice, KnockoutMice, TransgenicMultiple MyelomaPrevotellaTh17 CellsInterleukin-17

Identifiers

PMID30510245
PMCPMC6277390
OpenAlexW2901497217

What OpenQuestion holds

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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.