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LL-37

Cathelicidin, hCAP-18, FALL-39, CAP-18

Quick Stats
Studies 2230
Trials 95
Score 3
2013 pubmed 41 citations

LL-37 in periodontal health and disease and its susceptibility to degradation by proteinases present in gingival crevicular fluid.

McCrudden. Maelíosa T C MT; Orr. David F DF; Yu. Yang Y; Coulter. Wilson A WA; Manning. Gwen G; Irwin. Chris R CR; Lundy. Fionnuala T FT

Key Findings

  • LL-37 levels are higher in gum fluid from periodontitis patients than from healthy subjects.
  • Gingival crevicular fluid (GCF) from sites infected with P. gingivalis rapidly degrades added synthetic LL-37.
  • The degradation is driven by bacterial proteases (gingipains) and can be blocked by specific protease inhibitors.

Practical Outcomes

  • For DIY oral‑health protocols, plain LL-37 supplements are unlikely to survive in diseased gums, so using protease inhibitors or stable LL-37 mimetics would be more effective. If you’re experimenting with peptide‑based mouth rinses, consider formulations that protect the peptide from gingipain activity or target the bacterial enzymes directly.

Summary

LL-37, a natural antimicrobial peptide, is found in gum fluid both in healthy people and those with gum disease, but in diseased gums it gets broken down quickly by bacterial enzymes, especially when the bad bacteria Porphyromonas gingivalis is present. This means simply adding LL-37 to the mouth won’t work well unless it’s protected or modified.

Abstract

To determine the levels of LL-37 in and its susceptibility to degradation by components of gingival crevicular fluid (GCF) in periodontal health and disease. Levels of LL-37 in GCF from periodontitis patients and periodontally healthy subjects were determined by ELISA. In addition, degradation of synthetic/exogenous LL-37 by components of GCF in the presence and absence of inhibitors was determined by matrix-assisted laser desorption/ionization time of flight mass spectrometry. The concentration of native LL-37 in GCF from Porphyromonas gingivalis positive (Pg+) and P. gingivalis negative (Pg-) sites in periodontitis patients was significantly higher than in GCF from healthy subjects. When synthetic LL-37 was added to healthy GCF, the peptide was not degraded. Conversely, GCF from Pg+ sites rapidly degraded synthetic LL-37 which was prevented in the presence of Arg- and Lys- gingipain inhibitors. Synthetic LL-37 was degraded more slowly by GCF from Pg- sites. LL-37 is detectable in GCF in periodontal health and disease. The rapid degradation of synthetic LL-37 in periodontitis GCF, particularly in Pg+ sites, limits its role as a potential therapeutic in the gingival crevice. These results highlight the need to design stable peptide mimetics of LL-37 as future therapeutics in periodontitis.

Study Information

Provider

pubmed

Year

2013

Date

2013-08-18T00:00:00.000Z

DOI

10.1111/jcpe.12141

Citations

41

References

43