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LL-37

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

Quick Stats
Studies 2230
Trials 95
2011 pubmed 43 citations

LL-37 expression in the skin in systemic lupus erythematosus.

Sun. C-L CL; Zhang. F-Z FZ; Li. P P; Bi. L-Q LQ

Key Findings

  • LL‑37 levels are significantly increased in lupus‑affected skin
  • Plasmacytoid dendritic cells and IFN‑α are also elevated in the same skin samples
  • The amounts of LL‑37, pDCs, and IFN‑α are positively correlated

Practical Outcomes

  • For DIY health enthusiasts, this research doesn’t provide any direct actions, dosage advice, or protocols to improve longevity or performance. It mainly adds to the scientific understanding of lupus and suggests LL‑37 may play a role in autoimmune skin inflammation, but it isn’t currently useful for self‑directed health optimization.

Summary

The study found that people with the autoimmune disease lupus have higher levels of the peptide LL‑37, certain immune cells (pDCs), and a signaling molecule (IFN‑α) in their skin, and these three things tend to rise together.

Abstract

The objective of this study was to investigate the expression and relationship of LL-37, plasmacytoid dendritic cells (pDCs) and interferon-alpha (IFN-α) in skin in systemic lupus erythematosus (SLE), and their role in SLE pathogenesis. Skin biopsies were taken from nine SLE patients and six healthy volunteers. Expression of LL-37, pDCs and IFN-α in skin specimens and consecutive sections of skin was detected with an immunohistochemical technique (IH); the expression of LL-37 and pDCs in the samples was detected with in situ hybridization (ISH). The expression levels of LL-37, pDCs and IFN-α were significantly higher in SLE skin than in that of healthy controls (p < 0.001) with either the IH or the ISH technique, and the location of positive expression in consecutive sections was similar. Correlation analysis showed that the expression levels of LL-37, pDCs and IFN-α correlated positively with each other. In conclusion, the expression of LL-37, pDCs and IFN-α was increased in the skin of patients with active SLE. It is necessary to study further the role of LL-37 in the pathogenesis of SLE, and the exact relationship among LL-37, pDCs and IFN-α.

Study Information

Provider

pubmed

Year

2011

Date

2011-05-11T00:00:00.000Z

DOI

10.1177/0961203311398515

Citations

43

References

26