LL-37 Overview
Mechanism of Action
LL-37 is the only human cathelicidin antimicrobial peptide, a 37-amino-acid amphipathic alpha-helical peptide cleaved from the precursor protein hCAP-18. It directly disrupts microbial membranes (bacteria, fungi, viruses) and also serves as a potent immunomodulator — recruiting neutrophils, monocytes, and T cells to infection sites, promoting wound healing, and modulating inflammatory cytokine production.
~2–4 hours (tissue activity persists longer)
Timing
Morning
Injection Site
Subcutaneous, abdomen
Food
No restrictions
Common Stacks
- Thymosin Alpha-1 — Complementary immune modulation
- KPV — Anti-inflammatory synergy
- BPC-157 — Tissue repair + immune support
LL-37 Dosing Protocol
Immune Support Protocol
2–4 weeks50–100 mcg daily
Short-term immune boosting during acute illness or infection risk.
Maintenance
2 weeks on / 2 weeks off50 mcg daily
Cycling for long-term immune resilience.
LL-37 Expected Timeline
Day 1–3
Immune system activation; enhanced pathogen defense
Week 1–2
Improved infection resistance; anti-inflammatory effects
Week 2–4
Enhanced wound healing; sustained immune modulation
LL-37 Side Effects
Injection site redness
Mild fever-like sensation (immune activation)
Generally well tolerated
LL-37 Research Studies
LL-37, the only human member of the cathelicidin family of antimicrobial peptides
Vandamme D, Landuyt B, Luyten W, Schoofs L — Commun Integr Biol (2012)
Comprehensive review of LL-37’s dual role as both a direct antimicrobial agent and an immunomodulator that recruits immune cells and promotes tissue repair.
PubMed: 23060953Cathelicidin antimicrobial peptides and their role in innate immunity
Zanetti M — Curr Issues Mol Biol (2005)
Established the broad-spectrum antimicrobial activity of cathelicidins against gram-positive/negative bacteria, fungi, and enveloped viruses.
PubMed: 15580780LL-37 FAQ
Is LL-37 an antibiotic?
LL-37 is not a traditional antibiotic. It is a naturally occurring human antimicrobial peptide that kills pathogens by disrupting their cell membranes. Unlike antibiotics, bacteria have much greater difficulty developing resistance to LL-37 because it attacks a fundamental structural component of microbial membranes.
Can LL-37 help with biofilm infections?
Research suggests LL-37 can disrupt bacterial biofilms at concentrations below its direct antimicrobial threshold. It prevents biofilm formation and can break down established biofilms, making it potentially useful for chronic biofilm-associated infections.
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