Evidence map›Paper›PMID 29133782›Full record

ArticleNature communications2017

mTOR intersects antibody-inducing signals from TACI in marginal zone B cells.

Jordi Sintes, Maurizio Gentile, Shuling Zhang, Yolanda Garcia-Carmona, Giuliana Magri, Linda Cassis, Daniel Segura-Garzón, Alessandra Ciociola, Emilie K Grasset, Sabrina Bascones and 20 more

Open access · goldAbstract read
In one paragraph

Article in Nature communications, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 49 papers.

0numbers the graph read from it
0cells of the map it votes in
49citing papers in PubMed
2.3field-weighted citation impact, top 11% 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

49 citing papers in PubMed, 62 citations in OpenAlex.

  1. A guide to B cell metabolism.Nature reviews. Immunology · 2026
    Review
  2. Review
  3. Review
  4. TACI regulates marginal zone B cell development.The Journal of experimental medicine · 2026
    Article
  5. Article
  6. Article
  7. Article
  8. Immune mechanism ofFrontiers in immunology · 2025
    Article
  9. Article
  10. Article
  11. Article
  12. Article
  13. Article
  14. Article
  15. Article
  16. TACI and endogenous APRIL in B cell maturation.Clinical immunology (Orlando, Fla.) · 2023
    Article
  17. Article
  18. Autophagy-related mechanisms for treatment of multiple myeloma.Cancer drug resistance (Alhambra, Calif.) · 2023
    Review
  19. Article
  20. Review
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

30 authors at 9 institutions in 4 countries.

Jordi SintesProgram for Inflammatory and Cardiovascular Disorders, Institut Hospital del Mar d'Investigacions Mèdiques (IMIM), Barcelona, 08003, Spain. jsintes@imim.es.
Maurizio GentileProgram for Inflammatory and Cardiovascular Disorders, Institut Hospital del Mar d'Investigacions Mèdiques (IMIM), Barcelona, 08003, Spain.
Shuling ZhangLaboratory of Cancer Biology and Genetics, National Cancer Institute, National Institutes of Health, Bethesda, MD, 20892, USA.
Yolanda Garcia-CarmonaDepartment of Medicine and Pediatrics, Immunology Institute, Icahn School of Medicine at Mount Sinai, New York, NY, 10029, USA.
Giuliana MagriProgram for Inflammatory and Cardiovascular Disorders, Institut Hospital del Mar d'Investigacions Mèdiques (IMIM), Barcelona, 08003, Spain.
Linda CassisProgram for Inflammatory and Cardiovascular Disorders, Institut Hospital del Mar d'Investigacions Mèdiques (IMIM), Barcelona, 08003, Spain.
Daniel Segura-GarzónProgram for Inflammatory and Cardiovascular Disorders, Institut Hospital del Mar d'Investigacions Mèdiques (IMIM), Barcelona, 08003, Spain.
Alessandra CiociolaProgram for Inflammatory and Cardiovascular Disorders, Institut Hospital del Mar d'Investigacions Mèdiques (IMIM), Barcelona, 08003, Spain.
Emilie K GrassetDepartment of Medicine, Immunology Institute, Icahn School of Medicine at Mount Sinai, New York, NY, 10029, USA.
Sabrina BasconesProgram for Inflammatory and Cardiovascular Disorders, Institut Hospital del Mar d'Investigacions Mèdiques (IMIM), Barcelona, 08003, Spain.
Laura ComermaProgram for Inflammatory and Cardiovascular Disorders, Institut Hospital del Mar d'Investigacions Mèdiques (IMIM), Barcelona, 08003, Spain.
Marc PybusProgram for Inflammatory and Cardiovascular Disorders, Institut Hospital del Mar d'Investigacions Mèdiques (IMIM), Barcelona, 08003, Spain.
David LligéProgram for Inflammatory and Cardiovascular Disorders, Institut Hospital del Mar d'Investigacions Mèdiques (IMIM), Barcelona, 08003, Spain.
Irene PugaProgram for Inflammatory and Cardiovascular Disorders, Institut Hospital del Mar d'Investigacions Mèdiques (IMIM), Barcelona, 08003, Spain.
Cindy GutzeitDepartment of Medicine, Immunology Institute, Icahn School of Medicine at Mount Sinai, New York, NY, 10029, USA.
Bing HeDepartment of Medicine, Immunology Institute, Icahn School of Medicine at Mount Sinai, New York, NY, 10029, USA.
Wendy DuBoisLaboratory of Cancer Biology and Genetics, National Cancer Institute, National Institutes of Health, Bethesda, MD, 20892, USA.
Marta CrespoDepartment of Nephrology, Institut Hospital del Mar d'Investigacions Mèdiques (IMIM), Barcelona, 08003, Spain.
Julio PascualDepartment of Nephrology, Institut Hospital del Mar d'Investigacions Mèdiques (IMIM), Barcelona, 08003, Spain.
Anna MensaImmunology Service, Hospital Clínic of Barcelona, Barcelona, 08036, Spain.
Juan Ignacio ArósteguiImmunology Service, Hospital Clínic of Barcelona, Barcelona, 08036, Spain.
Manel JuanImmunology Service, Hospital Clínic of Barcelona, Barcelona, 08036, Spain.ORCID http://orcid.org/0000-0002-3064-1648
Jordi YagüeImmunology Service, Hospital Clínic of Barcelona, Barcelona, 08036, Spain.
Sergi SerranoDepartment of Pathology, Hospital del Mar, Barcelona, 08003, Spain.
Josep LloretaDepartment of Pathology, Hospital del Mar, Barcelona, 08003, Spain.
Eric MeffreDepartment of Immunobiology, Yale University, New Haven, CT, 06511, USA.
Michael HahneMolecular Genetics Institute of Montpellier, Montpellier, 34293, France.
Charlotte Cunningham-RundlesDepartment of Medicine and Pediatrics, Immunology Institute, Icahn School of Medicine at Mount Sinai, New York, NY, 10029, USA.
Beverly A MockLaboratory of Cancer Biology and Genetics, National Cancer Institute, National Institutes of Health, Bethesda, MD, 20892, USA.ORCID http://orcid.org/0000-0003-2479-4549
Andrea CeruttiProgram for Inflammatory and Cardiovascular Disorders, Institut Hospital del Mar d'Investigacions Mèdiques (IMIM), Barcelona, 08003, Spain. acerutti@imim.es.
Hospital del Mar Research Institute · ESHospital Clínic de Barcelona · ESIcahn School of Medicine at Mount Sinai · USNational Institutes of Health · USUniversitat Pompeu Fabra · ESInstitució Catalana de Recerca i Estudis Avançats · ESInstitut de Génétique Moléculaire de Montpellier · FRKarolinska University Hospital · SEYale University · US

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
Regulation of antibody production by innate signalsR01AI057653 · NIAID · WEILL MEDICAL COLL OF CORNELL UNIV · PI CERUTTI, ANDREA · 2005 to 2016
$4.3M
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 R01 AI057653NIAID NIH HHS U01 AI095613
6 · The paper itself

Abstract

Mechanistic target of rapamycin (mTOR) enhances immunity in addition to orchestrating metabolism. Here we show that mTOR coordinates immunometabolic reconfiguration of marginal zone (MZ) B cells, a pre-activated lymphocyte subset that mounts antibody responses to T-cell-independent antigens through a Toll-like receptor (TLR)-amplified pathway involving transmembrane activator and CAML interactor (TACI). This receptor interacts with mTOR via the TLR adapter MyD88. The resulting mTOR activation instigates MZ B-cell proliferation, immunoglobulin G (IgG) class switching, and plasmablast differentiation through a rapamycin-sensitive pathway that integrates metabolic and antibody-inducing transcription programs, including NF-κB. Disruption of TACI-mTOR interaction by rapamycin, truncation of the MyD88-binding domain of TACI, or B-cell-conditional mTOR deficiency interrupts TACI signaling via NF-κB and cooperation with TLRs, thereby hampering IgG production to T-cell-independent antigens but not B-cell survival. Thus, mTOR drives innate-like antibody responses by linking proximal TACI signaling events with distal immunometabolic transcription programs.

Indexed as

AnimalsB-LymphocytesCell LineCell ProliferationEnzyme ActivationGene Expression ProfilingHEK293 CellsHumansImmunoglobulin Class SwitchingImmunoglobulin GLymphocyte ActivationMechanistic Target of Rapamycin Complex 1MiceMice, Inbred C57BLMice, KnockoutMyeloid Differentiation Factor 88Immunoglobulin GMechanistic Target of Rapamycin Complex 1MTOR protein, humanMYD88 protein, humanMyeloid Differentiation Factor 88NF-kappa BSirolimusTNFRSF13B protein, humanTOR Serine-Threonine KinasesTransmembrane Activator and CAML Interactor Protein

Identifiers

PMID29133782
PMCPMC5684130
OpenAlexW2767226775

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.