Evidence map›Paper›PMID 24684957›Full record

ArticleImmunity2014

Segmented filamentous bacteria antigens presented by intestinal dendritic cells drive mucosal Th17 cell differentiation.

Yoshiyuki Goto, Casandra Panea, Gaku Nakato, Anna Cebula, Carolyn Lee, Marta Galan Diez, Terri M Laufer, Leszek Ignatowicz, Ivaylo I Ivanov

Open access · bronzeAbstract read
In one paragraph

Article in Immunity, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 297 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
297citing papers in PubMed, 1 pooled it
23.9field-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

297 citing papers in PubMed, 1 synthesis or guideline pooled it, 448 citations in OpenAlex.

  1. Pooled it
  2. Review
  3. Review
  4. Review
  5. Gut microbiota in health and disease.Molecular biomedicine · 2026
    Review
  6. Review
  7. Review
  8. Article
  9. Contextualizing TNature reviews. Immunology · 2026
    Review
  10. Review
  11. Review
  12. Effect of the intestinal microbiota on TSeminars in immunopathology · 2026
    Review
  13. Review
  14. Article
  15. Article
  16. Review
  17. Article
  18. Review
  19. Review
  20. Review

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

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

9 authors at 3 institutions in 1 country.

Yoshiyuki GotoDepartment of Microbiology and Immunology, Columbia University Medical Center, New York, NY 10032, USA.
Casandra PaneaDepartment of Microbiology and Immunology, Columbia University Medical Center, New York, NY 10032, USA.
Gaku NakatoDepartment of Microbiology and Immunology, Columbia University Medical Center, New York, NY 10032, USA.
Anna CebulaCenter for Biotechnology and Genomic Medicine, Georgia Regents University, Augusta, GA 30912, USA.
Carolyn LeeDepartment of Microbiology and Immunology, Columbia University Medical Center, New York, NY 10032, USA.
Marta Galan DiezDepartment of Microbiology and Immunology, Columbia University Medical Center, New York, NY 10032, USA.
Terri M LauferDepartment of Medicine, Perelman School of Medicine, University of Pennsylvania and Philadelphia Veterans Affairs Medical Center, Philadelphia, PA 19104, USA.
Leszek IgnatowiczCenter for Biotechnology and Genomic Medicine, Georgia Regents University, Augusta, GA 30912, USA.
Ivaylo I IvanovDepartment of Microbiology and Immunology, Columbia University Medical Center, New York, NY 10032, USA. Electronic address: ii2137@columbia.edu.
Columbia University Irving Medical Center · USAugusta University · USUniversity of Pennsylvania · US

Funding

Role of intestinal commensal-induced Th17 cells and mucosal immunity in metabolic diseaseR01DK098378 · NIDDK · COLUMBIA UNIVERSITY HEALTH SCIENCES · PI Ivaylo Ivanov Ivanov · 2013 to 2026
$6.5M
NIDDK NIH HHS 1R01DK098378NIDDK NIH HHS R01 DK098378
6 · The paper itself

Abstract

How commensal microbiota contributes to immune cell homeostasis at barrier surfaces is poorly understood. Lamina propria (LP) T helper 17 (Th17) cells participate in mucosal protection and are induced by commensal segmented filamentous bacteria (SFB). Here we show that MHCII-dependent antigen presentation of SFB antigens by intestinal dendritic cells (DCs) is crucial for Th17 cell induction. Expression of MHCII on CD11c(+) cells was necessary and sufficient for SFB-induced Th17 cell differentiation. Most SFB-induced Th17 cells recognized SFB in an MHCII-dependent manner. SFB primed and induced Th17 cells locally in the LP and Th17 cell induction occurred normally in mice lacking secondary lymphoid organs. The importance of other innate cells was unveiled by the finding that MHCII deficiency in group 3 innate lymphoid cells (ILCs) resulted in an increase in SFB-independent Th17 cell differentiation. Our results outline the complex role of DCs and ILCs in the regulation of intestinal Th17 cell homeostasis.

Indexed as

AnimalsAntigen PresentationAntigens, BacterialCell DifferentiationCells, CulturedClostridiumClostridium InfectionsDendritic CellsHistocompatibility Antigens Class IIIntestinesLymphocyte ActivationLymphocytesMiceMice, KnockoutMice, TransgenicMicrobiotaAntigens, BacterialHistocompatibility Antigens Class IINuclear Receptor Subfamily 1, Group F, Member 3

Identifiers

PMID24684957
PMCPMC4084624
OpenAlexW2004714320

What OpenQuestion holds

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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.