Evidence map›Paper›PMID 24562309›Full record

ArticleNature immunology2014

Innate lymphoid cells integrate stromal and immunological signals to enhance antibody production by splenic marginal zone B cells.

Giuliana Magri, Michio Miyajima, Sabrina Bascones, Arthur Mortha, Irene Puga, Linda Cassis, Carolina M Barra, Laura Comerma, Aleksey Chudnovskiy, Maurizio Gentile and 9 more

Open access · greenAbstract read
In one paragraph

Article in Nature immunology, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 165 papers.

0numbers the graph read from it
0cells of the map it votes in
165citing papers in PubMed
16.5field-weighted citation impact, top 1% 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

165 citing papers in PubMed, 271 citations in OpenAlex.

  1. Trial
  2. Review
  3. Review
  4. Article
  5. Review
  6. Engineered CD40-biosensor-expressing Treg cells as a cell therapy approach for inflammatory diseases.Molecular therapy : the journal of the American Society of Gene Therapy · 2026
    Article
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  8. Review
  9. Review
  10. Article
  11. Article
  12. Review
  13. Article
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  15. Article
  16. Article
  17. Intestinal CXCR6Immunity · 2024
    Article
  18. Article
  19. Article
  20. Review

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

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

19 authors at 6 institutions in 3 countries.

Giuliana Magri *Institut Hospital del Mar d'Investigacions Mèdiques, Barcelona, Spain.
Michio Miyajima *Laboratory for Mucosal Immunity, RIKEN Center for Integrative Medical Sciences, RIKEN Yokohama, Tsurumi, Yokohama, Japan.
Sabrina BasconesInstitut Hospital del Mar d'Investigacions Mèdiques, Barcelona, Spain.
Arthur MorthaTisch Cancer Institute, Department of Medicine, Icahn School of Medicine at Mount Sinai, New York, New York, USA.
Irene PugaInstitut Hospital del Mar d'Investigacions Mèdiques, Barcelona, Spain.
Linda CassisInstitut Hospital del Mar d'Investigacions Mèdiques, Barcelona, Spain.
Carolina M BarraInstitut Hospital del Mar d'Investigacions Mèdiques, Barcelona, Spain.
Laura ComermaInstitut Hospital del Mar d'Investigacions Mèdiques, Barcelona, Spain.
Aleksey ChudnovskiyTisch Cancer Institute, Department of Medicine, Icahn School of Medicine at Mount Sinai, New York, New York, USA.
Maurizio GentileInstitut Hospital del Mar d'Investigacions Mèdiques, Barcelona, Spain.
David LligeInstitut Hospital del Mar d'Investigacions Mèdiques, Barcelona, Spain.
Montserrat ColsImmunology Institute, Department of Medicine, Icahn School of Medicine at Mount Sinai, New York, New York, USA.
Sergi SerranoDepartment of Pathology, Hospital del Mar, Universitat Autònoma de Barcelona and Universitat Pompeu Fabra, Barcelona, Spain.
Juan Ignacio ArósteguiImmunology Service, Hospital Clínic of Barcelona, Barcelona, Spain.
Manel JuanImmunology Service, Hospital Clínic of Barcelona, Barcelona, Spain.
Jordi YagüeImmunology Service, Hospital Clínic of Barcelona, Barcelona, Spain.
Miriam MeradTisch Cancer Institute, Department of Medicine, Icahn School of Medicine at Mount Sinai, New York, New York, USA.
Sidonia FagarasanLaboratory for Mucosal Immunity, RIKEN Center for Integrative Medical Sciences, RIKEN Yokohama, Tsurumi, Yokohama, Japan.
Andrea CeruttiInstitut Hospital del Mar d'Investigacions Mèdiques, Barcelona, Spain.
Hospital del Mar Research Institute · ESIcahn School of Medicine at Mount Sinai · USHospital Clínic de Barcelona · ESRIKEN Center for Integrative Medical Sciences · JPBarcelona Biomedical Research Park · ESPompeu Fabra University · ES

Funding

Regulation of IgA class switching in the intestinal mucosaP01AI061093 · NIAID · MOUNT SINAI SCHOOL OF MEDICINE OF NYU · PI CUNNINGHAM-RUNDLES, CHARLOTTE · 2004 to 2021
$29.8M
Role of Follicular T Helper Cells In Enhancing Humoral Immunity and ProtectionU19AI096187 · NIAID · EMORY UNIVERSITY · PI DERDEYN, CYNTHIA ANN · 2011 to 2015
$26.5M
Human MAIT celis in airway mucosal immune responses to intracellular infectionsU01AI095776 · NIAID · OREGON HEALTH & SCIENCE UNIVERSITY · PI LEWINSOHN, DAVID M. · 2011 to 2015
$8.9M
Regulation of antibody production by innate signalsR01AI057653 · NIAID · WEILL MEDICAL COLL OF CORNELL UNIV · PI CERUTTI, ANDREA · 2005 to 2016
$4.3M
Regulation of antibody diversification and production in HIV-1 infectionR01AI074378 · NIAID · WEILL MEDICAL COLL OF CORNELL UNIV · PI CERUTTI, ANDREA · 2008 to 2012
$2.1M
Regulation and Function of Immunoglobulin D in Mucosal Immune DefenseU01AI095613 · NIAID · ICAHN SCHOOL OF MEDICINE AT MOUNT SINAI · PI CERUTTI, ANDREA · 2011 to 2015
$2.1M
NIAID NIH HHS P01 AI061093NIAID NIH HHS P01 AI61093NIAID NIH HHS R01 AI057653NIAID NIH HHS R01 AI074378NIAID NIH HHS R01 AI57653NIAID NIH HHS R01 AI74378NIAID NIH HHS U01 AI095613NIAID NIH HHS U01 AI095776NIAID NIH HHS U01 AI95613NIAID NIH HHS U01 AI95776NIAID NIH HHS U19 AI096187
6 · The paper itself

Abstract

Innate lymphoid cells (ILCs) regulate stromal cells, epithelial cells and cells of the immune system, but their effect on B cells remains unclear. Here we identified RORγt(+) ILCs near the marginal zone (MZ), a splenic compartment that contains innate-like B cells highly responsive to circulating T cell-independent (TI) antigens. Splenic ILCs established bidirectional crosstalk with MAdCAM-1(+) marginal reticular cells by providing tumor-necrosis factor (TNF) and lymphotoxin, and they stimulated MZ B cells via B cell-activation factor (BAFF), the ligand of the costimulatory receptor CD40 (CD40L) and the Notch ligand Delta-like 1 (DLL1). Splenic ILCs further helped MZ B cells and their plasma-cell progeny by coopting neutrophils through release of the cytokine GM-CSF. Consequently, depletion of ILCs impaired both pre- and post-immune TI antibody responses. Thus, ILCs integrate stromal and myeloid signals to orchestrate innate-like antibody production at the interface between the immune system and circulatory system.

Indexed as

Antibody FormationAnimalsAntibodiesAntigens, T-IndependentBlood ProteinsB-LymphocytesCell Adhesion MoleculesCell CommunicationCell DifferentiationCells, CulturedGranulocyte-Macrophage Colony-Stimulating FactorHumansImmunity, InnateImmunoglobulinsLymphocyte ActivationLymphocytesAntibodiesAntigens, T-IndependentBlood ProteinsCell Adhesion MoleculesGranulocyte-Macrophage Colony-Stimulating FactorImmunoglobulinsMADCAM1 protein, humanMucoproteinsNuclear Receptor Subfamily 1, Group F, Member 3Picratespicric acid

Identifiers

PMID24562309
PMCPMC4005806
OpenAlexW2089077748

What OpenQuestion holds

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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.