Evidence map›Paper›PMID 28542929›Full record

ReviewImmunology2017

The immune response to Prevotella bacteria in chronic inflammatory disease.

Jeppe Madura Larsen

Open access · bronzeAbstract readReview
In one paragraph

Review in Immunology, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 843 papers, 7 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
843citing papers in PubMed, 7 pooled it
26.8field-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

843 citing papers in PubMed, 7 syntheses or guidelines pooled it, 1,349 citations in OpenAlex.

  1. Guideline
  2. Biopsychosocial and Environmental Factors That Impact Brain-Gut-Microbiome Interactions in Obesity.Clinical gastroenterology and hepatology : the official clinical practice journal of the American Gastroenterological Association · 2026
    Pooled it
  3. Pooled it
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  7. Pooled it
  8. Effect ofNutrients · 2026
    Trial
  9. Trial
  10. Efficacy ofFrontiers in nutrition · 2026
    Trial
  11. Trial
  12. Trial
  13. Trial
  14. Article
  15. Bridging the gap:Gut microbes · 2026
    Review
  16. Article
  17. Article
  18. Article
  19. Article
  20. Live AirwayEnvironment & health (Washington, D.C.) · 2026
    Article

783 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

1 author at 1 institution in 1 country.

Jeppe Madura LarsenDepartment of Technology, Faculty of Health and Technology, Metropolitan University College, Copenhagen, Denmark.ORCID 0000-0003-1492-0708
Metropolitan University College · DK

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The microbiota plays a central role in human health and disease by shaping immune development, immune responses and metabolism, and by protecting from invading pathogens. Technical advances that allow comprehensive characterization of microbial communities by genetic sequencing have sparked the hunt for disease-modulating bacteria. Emerging studies in humans have linked the increased abundance of Prevotella species at mucosal sites to localized and systemic disease, including periodontitis, bacterial vaginosis, rheumatoid arthritis, metabolic disorders and low-grade systemic inflammation. Intriguingly, Prevotella abundance is reduced within the lung microbiota of patients with asthma and chronic obstructive pulmonary disease. Increased Prevotella abundance is associated with augmented T helper type 17 (Th17) -mediated mucosal inflammation, which is in line with the marked capacity of Prevotella in driving Th17 immune responses in vitro. Studies indicate that Prevotella predominantly activate Toll-like receptor 2, leading to production of Th17-polarizing cytokines by antigen-presenting cells, including interleukin-23 (IL-23) and IL-1. Furthermore, Prevotella stimulate epithelial cells to produce IL-8, IL-6 and CCL20, which can promote mucosal Th17 immune responses and neutrophil recruitment. Prevotella-mediated mucosal inflammation leads to systemic dissemination of inflammatory mediators, bacteria and bacterial products, which in turn may affect systemic disease outcomes. Studies in mice support a causal role of Prevotella as colonization experiments promote clinical and inflammatory features of human disease. When compared with strict commensal bacteria, Prevotella exhibit increased inflammatory properties, as demonstrated by augmented release of inflammatory mediators from immune cells and various stromal cells. These findings indicate that some Prevotella strains may be clinically important pathobionts that can participate in human disease by promoting chronic inflammation.

Indexed as

ImmunityAnimalsBacteroidaceae InfectionsChronic DiseaseCytokinesHigh-Throughput Nucleotide SequencingHumansImmunomodulationInflammationIntestinal MucosaMicrobiotaPrevotellaTh17 CellsToll-Like Receptor 2CytokinesToll-Like Receptor 2cytokinesinflammationinflammatory diseasemucosaPrevotellaT cells

Identifiers

PMID28542929
PMCPMC5506432
OpenAlexW2618503740

What OpenQuestion holds

Textmetadata
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.