Evidence map›Paper›PMID 12522054›Full record

ArticleClinical and diagnostic laboratory immunology2003

Keratinocyte expression of human beta defensin 2 following bacterial infection: role in cutaneous host defense.

James G H Dinulos, Laurel Mentele, L Page Fredericks, Beverly A Dale, Gary L Darmstadt

Open access · diamondAbstract read
In one paragraph

Article in Clinical and diagnostic laboratory immunology, 2003. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 30 papers.

0numbers the graph read from it
0cells of the map it votes in
30citing papers in PubMed
4.7field-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

30 citing papers in PubMed, 82 citations in OpenAlex.

  1. Trial
  2. Induction of Human β-Defensin-2 by VaginalOpen forum infectious diseases · 2026
    Article
  3. Review
  4. Article
  5. Review
  6. Towards sustainable antimicrobial therapies forSustainable microbiology · 2024
    Review
  7. Detection of Antimicrobial Peptides in Stratum Corneum by Mass Spectrometry.International journal of molecular sciences · 2021
    Article
  8. Article
  9. Review
  10. Article
  11. Review
  12. Observational
  13. Article
  14. Review
  15. Review
  16. Toll-like receptors and skin cancer.Frontiers in immunology · 2014
    Review
  17. Effects of yoga exercise on salivary beta-defensin 2.European journal of applied physiology · 2013
    Article
  18. Article
  19. Review
  20. Article
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

5 authors at 3 institutions in 1 country.

James G H DinulosDivision of Dermatology, Department of Medicine, University of Washington, Seattle, Washington , USA.
Laurel Mentele
L Page Fredericks
Beverly A Dale
Gary L Darmstadt
Johns Hopkins University · USSeattle Children's Hospital · USUniversity of Washington · US

Funding

Regulation of Beta-Defensin Expression in Oral EpitheliaR01DE013573 · NIDCR · UNIVERSITY OF WASHINGTON · PI CHUNG, WHASUN OH · 2000 to 2009
$3.1M
CORE--LABORATORYP30HD028834 · NICHD · UNIVERSITY OF WASHINGTON · PI ABELSON, HERBERT T · 1992 to 2002
$1.1M
DERMATOLOGY TRAININGT32AR007019 · NIAMS · UNIVERSITY OF WASHINGTON · PI OLERUD, JOHN EVERETT · 1986 to 2005
$957k
NIAMS NIH HHS T32 AR007019NIAMS NIH HHS T32AR07019NICHD NIH HHS P30 HD28834NIDCR NIH HHS R01 DE013573NIDCR NIH HHS R01DE13573
6 · The paper itself

Abstract

Human beta defensin 2 (hbetaD-2) is thought to play an important role in cutaneous immune defense. We hypothesized that (i) keratinocyte expression of hbetaD-2, measured by reverse transcription-PCR, would be upregulated in response to challenge with pathogenic bacteria, particularly highly adherent strains of Streptococcus pyogenes and Staphylococcus aureus, and (ii) hbetaD-2 would have potent antimicrobial activity against pathogenic but not commensal organisms. Expression of hbetaD-2 was induced consistently by S. aureus, Staphylococcus epidermidis, Escherichia coli, and Pseudomonas aeruginosa, whereas strains of S. pyogenes were poor and variable inducers of hbetaD-2. No correlation was found between levels of bacterial adherence and keratinocyte expression of hbetaD-2. S. pyogenes was significantly more sensitive to killing by hbetaD-2 than S. epidermidis. We conclude that the ability to induce hbetaD-2 expression in combination with sensitivity to its antimicrobial effects may contribute to the rarity of skin infections with the gram-negative bacterial organisms, whereas lack of stimulation of hbetaD-2 expression by S. pyogenes may be important in its ability to evade innate defenses and cause skin disease. Induction of expression of hbetaD-2 but relative tolerance to it may enable S. epidermidis to survive on the skin surface and modulate hbetaD-2 expression when the stratum corneum barrier is disrupted.

Indexed as

Bacterial AdhesionBacterial Infectionsbeta-DefensinsHumansKeratinocytesSkinSkin DiseasesStaphylococcus epidermidisStreptococcus pyogenesUp-Regulationbeta-DefensinsDEFB4A protein, human

Identifiers

PMID12522054
PMCPMC145269
OpenAlexW2125985831

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.