Evidence map›Paper›PMID 24721570›Full record

ArticleCell host & microbe2014

Plasmacytoid dendritic cells mediate anti-inflammatory responses to a gut commensal molecule via both innate and adaptive mechanisms.

Suryasarathi Dasgupta, Deniz Erturk-Hasdemir, Javier Ochoa-Reparaz, Hans-Christian Reinecker, Dennis L Kasper

Open access · bronzeAbstract read
In one paragraph

Article in Cell host & microbe, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 186 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
186citing papers in PubMed, 2 pooled it
8.7field-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

186 citing papers in PubMed, 2 syntheses or guidelines pooled it, 287 citations in OpenAlex.

  1. Pooled it
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  3. Trial
  4. Review
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  6. Article
  7. Current research in microbial sciences · 2026
    Article
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  9. Article
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  11. Article
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  15. Synthesis and Docking Studies of Glycolipids Inspired byMolecules (Basel, Switzerland) · 2025
    Article
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126 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

5 authors at 3 institutions in 1 country.

Suryasarathi DasguptaDivision of Immunology, Department of Microbiology and Immunobiology, Harvard Medical School, Boston, MA 02115, USA.
Deniz Erturk-HasdemirDivision of Immunology, Department of Microbiology and Immunobiology, Harvard Medical School, Boston, MA 02115, USA.
Javier Ochoa-ReparazCenter for Nanomedicine, Sanford-Burnham Medical Research Institute at the University of California, Santa Barbara, CA 93106-9625, USA.
Hans-Christian ReineckerDivision of Gastroenterology, Massachusetts General Hospital, Boston, MA 02114, USA.
Dennis L KasperDivision of Immunology, Department of Microbiology and Immunobiology, Harvard Medical School, Boston, MA 02115, USA. Electronic address: dennis_kasper@hms.harvard.edu.
Harvard University · USMassachusetts General Hospital · USUniversity of California, Santa Barbara · US

Funding

Pilot & Feasibility ProgramP30DK043351 · NIDDK · MASSACHUSETTS GENERAL HOSPITAL · PI RAYMOND T CHUNG · 1991 to 2026
$35.3M
Antigen Recognition at Intestinal Epithelial InterphasesR01DK068181 · NIDDK · MASSACHUSETTS GENERAL HOSPITAL · PI REINECKER, HANS-CHRISTIAN · 2005 to 2017
$5.2M
Commensal Bacteroides signal through sphingolipid rafts during intestinal stressR21AI090102 · NIAID · HARVARD MEDICAL SCHOOL · PI KASPER, DENNIS L. · 2011 to 2012
$470k
NIAID NIH HHS AI1090102NIAID NIH HHS R21 AI090102NIDDK NIH HHS P30 DK043351NIDDK NIH HHS R01 DK068181
6 · The paper itself

Abstract

Polysaccharide A (PSA), the archetypical immunomodulatory molecule of the gut commensal Bacteroides fragilis, induces regulatory T cells to secrete the anti-inflammatory cytokine interleukin-10 (IL-10). The cellular mediators of PSA's immunomodulatory properties are incompletely understood. In a mouse model of colitis, we find that PSA requires both innate and adaptive immune mechanisms to generate protection. Plasmacytoid DCs (PDCs) exposed to PSA do not produce proinflammatory cytokines, but instead they specifically stimulate IL-10 secretion by CD4+ T cells and efficiently mediate PSA-afforded immunoprotection. PSA induces and preferentially ligates Toll-like receptor 2 on PDCs but not on conventional DCs. Compared with other TLR2 ligands, PSA is better at enhancing PDC expression of costimulatory molecules required for protection against colitis. PDCs can thus orchestrate the beneficial immunoregulatory interaction of commensal microbial molecules, such as PSA, through both innate and adaptive immune mechanisms.

Indexed as

Adaptive ImmunityAdoptive TransferAnimalsB7-1 AntigenB7-2 AntigenBacteroides fragilisBone Marrow CellsCD28 AntigensCD4-Positive T-LymphocytesCells, CulturedDendritic CellsEncephalomyelitis, Autoimmune, ExperimentalFemaleGastrointestinal TractImmunity, InnateInducible T-Cell Co-Stimulator LigandB7-1 AntigenB7-2 AntigenCD28 AntigensCd86 protein, mouseIcosl protein, mouseIL10 protein, mouseInducible T-Cell Co-Stimulator LigandInterleukin-10Polysaccharides, BacterialTlr2 protein, mouseToll-Like Receptor 2

Identifiers

PMID24721570
PMCPMC4020153
OpenAlexW2084891825

What OpenQuestion holds

Textmetadata
LicenceTDM
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.