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LL-37

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

Quick Stats
Studies 2230
Trials 95
Score 2
2020 pubmed 3 citations

Antimicrobial Peptide Omiganan Enhances Interferon Responses to Endosomal Toll-Like Receptor Ligands in Human Peripheral Blood Mononuclear Cells.

Grievink. Hendrika W HW; Jirka. Silvana M G SMG; Woutman. Tess D TD; Schoonakker. Mascha M; Rissmann. Robert R; Malone. Karen E KE; Feiss. Gary G; Moerland. Matthijs M

Key Findings

  • Omiganan increases interferon‑α release from human peripheral blood mononuclear cells when endosomal TLR3, TLR7, TLR8, or TLR9 are activated.
  • Plasmacytoid dendritic cells are the primary contributors to the enhanced interferon response.
  • The peptide shows potential as a treatment for virus‑driven diseases, but the exact molecular mechanism is still unknown.

Practical Outcomes

  • At this stage, there’s no clear protocol, dosage, or safety data for personal use, so biohackers should not try omiganan on their own. The finding may guide future development of immune‑boosting supplements or therapies, but more research and clinical trials are needed before it becomes a practical tool.

Summary

A lab study found that the synthetic peptide omiganan can boost the body's antiviral signaling (type I interferon) when immune cells are triggered by certain viral‑like sensors. The effect seems to come mainly from a special immune cell type called plasmacytoid dendritic cells. While this hints that omiganan could one day help fight viral infections, the research is still early and done only in test‑tube cells.

Abstract

LL-37 is a cationic antimicrobial peptide and the sole human member of cathelicidins. Besides its bactericidal properties, LL-37 is known to have direct immunomodulatory effects, among which enhancement of antiviral responses via endosomal toll-like receptors (TLRs). Omiganan pentahydrochloride is a synthetic cationic peptide in clinical development. Previously, omiganan was primarily known for its direct bactericidal and antifungal properties. We investigated whether omiganan enhances endosomal TLR responses, similar to LL-37. Human peripheral blood mononuclear cells were treated with endosomal TLR3, -7, -8, and -9 ligands in the presence of omiganan. Omiganan enhanced TLR-mediated interferon-α release. Subsequent experiments with TLR9 ligands showed that plasmacytoid dendritic cells were main contributors to omiganan-enhanced IFN production. Based on this type I interferon-enhancing effect, omiganan may qualify as potential treatment modality for virus-driven diseases. The molecular mechanism by which omiganan enhances endosomal TLR responses remains to be elucidated.

Study Information

Provider

pubmed

Year

2020

Date

2020-04-21T00:00:00.000Z

DOI

10.1111/cts.12789

Citations

3

References

28