Evidence map›Paper›PMID 24416190›Full record

ArticlePloS one2014

Immune mediated shaping of microflora community composition depends on barrier site.

Felix Scholz, Brian D Badgley, Michael J Sadowsky, Daniel H Kaplan

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed
5.6field-weighted citation impact, top 4% 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

22 citing papers in PubMed, 39 citations in OpenAlex.

  1. Langerhans cells: Central players in the pathophysiology of atopic dermatitis.Journal of the European Academy of Dermatology and Venereology : JEADV · 2025
    Review
  2. Article
  3. Review
  4. Review
  5. Article
  6. Review
  7. Article
  8. Article
  9. Review
  10. Skin-Associated B Cells in Health and Inflammation.Journal of immunology (Baltimore, Md. : 1950) · 2019
    Review
  11. Article
  12. Review
  13. Article
  14. Article
  15. Langerhans Cells Suppress CD49a+ NK Cell-Mediated Skin Inflammation.Journal of immunology (Baltimore, Md. : 1950) · 2015
    Article
  16. Interactions between host factors and the skin microbiome.Cellular and molecular life sciences : CMLS · 2015
    Review
  17. Article
  18. Article
  19. Review
  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

4 authors at 1 institution in 1 country.

Felix ScholzDepartment of Dermatology, Center for Immunology, University of Minnesota, Minneapolis, Minnesota, United States of America.
Brian D BadgleyBioTechnology Institute, University of Minnesota, Minneapolis, Minnesota, United States of America.
Michael J SadowskyBioTechnology Institute, University of Minnesota, Minneapolis, Minnesota, United States of America.
Daniel H KaplanDepartment of Dermatology, Center for Immunology, University of Minnesota, Minneapolis, Minnesota, United States of America.
University of Minnesota · US

Funding

MINNESOTA PAIN RESEARCH TRAINING PROGRAMT32DE007288 · NIDCR · UNIVERSITY OF MINNESOTA TWIN CITIES · PI HERZBERG, MARK C · 1996 to 2011
$8.8M
Role of Langerhans Cells in the Cutaneous Immune SystemR01AR056632 · NIAMS · UNIVERSITY OF MINNESOTA · PI KAPLAN, DANIEL H · 2009 to 2013
$1.6M
NIAMS NIH HHS AR056632NIAMS NIH HHS R01 AR056632NIDCR NIH HHS T32 DE007288NIDCR NIH HHS T32DE07288
6 · The paper itself

Abstract

Barrier surfaces, such as the intestinal lining and the skin, are colonized by a diverse community of commensal microorganisms. Although commensal microorganisms clearly impact the host immune system, whether the immune system also shapes the commensal community is poorly understood. We used 16S rDNA deep sequencing to test whether mice with specific immune defects have an altered commensal microflora. Initially, skin swabs were obtained from wild-type and Langerhans Cell (LC) deficient mice. Despite the intimate contacts that LC make with the upper epidermis, no significant differences were observed in microbial community composition. Similarly, the skin of MyD88/TRIF(-/-), Rag1(-/-) and heterozygous littermate controls showed no alteration in their commensal communities. Next we examined mouth swabs and feces. We did not find a difference in the MyD88/TRIF(-/-) mice. However, we did observe a significant shift in the microbial composition in the feces and mouths of Rag1(-/-) mice. Thus, we conclude that the adaptive immune system modulates the microbial composition at mucosal surfaces in the steady-state but LC, adaptive immunity, and MyD88-dependent innate responses do not affect the skin microbiome revealing a major distinction between barrier sites.

Indexed as

Adaptive ImmunityAdaptor Proteins, Vesicular TransportAnimalsColonHomeodomain ProteinsImmune SystemImmunity, InnateIntestinal MucosaLangerhans CellsMiceMice, Inbred C57BLMicrobiotaMouthMyeloid Differentiation Factor 88SkinAdaptor Proteins, Vesicular TransportHomeodomain ProteinsMyeloid Differentiation Factor 88RAG-1 proteinTicam1 protein, mouse

Identifiers

PMID24416190
PMCPMC3885526
OpenAlexW2074630587

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.