⚠ RESEARCH USE ONLY · NOT FDA-APPROVED FOR HUMAN USE · NOT MEDICAL ADVICE
IMMUNERESEARCH

LL-37.

Your body's natural antibiotic — in a vial
AKA · Cathelicidin · CAMP-derived peptide
IMMUNEHEALINGSUBCUTANEOUSTOPICAL

LL-37 is the only human member of the cathelicidin antimicrobial peptide family. It kills bacteria, fungi, and viruses directly while also modulating immune responses. A serious compound with serious tradeoffs.

~1 hour (free) / extended in tissue
Half-life
3
Citations
2
Routes
2
Categories
68
Popularity

AT A GLANCE.

§ 01 · TL;DR

THE QUICK READ.

LL-37 is the only human member of the cathelicidin antimicrobial peptide family. It kills bacteria, fungi, and viruses directly while also modulating immune responses. A serious compound with serious tradeoffs.

Punches holes in microbial cell membranes. Also tells your immune system to amp up the appropriate response.

Short cycles. Not for chronic autoimmune conditions.

WHAT IT MIGHT HELP WITH.

1
Broad-spectrum antimicrobial activity
2
Active against biofilm-forming bacteria
3
Modulates immune responses (pro- or anti-inflammatory depending on context)
4
Wound healing support in chronic wounds
5
Investigated for antibiotic-resistant infections

HOW IT WORKS.

§ 02 · MECHANISM

Punches holes in microbial cell membranes. Also tells your immune system to amp up the appropriate response.

37-residue α-helical amphipathic cationic peptide. Disrupts negatively charged microbial membranes via carpet/toroidal pore formation. Secondary immunomodulatory effects via FPR2 receptor activation influence monocyte, neutrophil, and T-cell recruitment.

WHO IT'S FOR
  • Antimicrobial research
  • Chronic biofilm infection models
WHO SHOULD AVOID
  • Psoriasis
  • Lupus / autoimmune conditions
  • Pregnancy

THE RESEARCH.

§ 03 · 3 STUDIES
2013 · FINDING

Duplantier & van Hoek — antimicrobial

Review: LL-37 active against MRSA, E. coli, Candida, P. aeruginosa including biofilms.

2008 · FINDING

Carretero et al. — wound healing

Topical LL-37 accelerated closure of chronic venous leg ulcers in Phase II.

2007 · FINDING

Lande et al. — autoimmunity

LL-37 complexes with self-DNA drive plasmacytoid DC activation in psoriasis.

DOSING PROTOCOL.

§ 04 · DOSING
TYPICAL RANGE
Short cycles. Not for chronic autoimmune conditions.
100–500mcg subcutaneous, 2–3x weekly (highly variable)
FREQUENCY
Most-cited schedule
Intermittent — not daily
ROUTES
Delivery methods
SUBCUTANEOUS · TOPICAL
HALF-LIFE
Steady state drives frequency
~1 hour (free) / extended in tissue
⚠ NOTE

These are reported protocols from research literature and practitioner accounts, not prescriptions. No FDA-approved human dose exists for research compounds. Anyone using LL-37 should work with a qualified physician and source from a supplier providing third-party COAs.

FORMS AVAILABLE
  • · Lyophilized vial, 5mg typical
⚠ RESEARCH INFORMATION ONLY · NOT MEDICAL ADVICE

SIDE EFFECTS & RISKS.

§ 06 · SAFETY
·
Injection site reactions
Common · mild
Transient flu-like symptoms
Reported · moderate

Immune activation

!
Hemolysis at high doses
Dose-dependent · serious
!
Potential autoimmune flare
Theoretical · serious

LL-37 is implicated in psoriasis/lupus pathology

WHERE TO SOURCE

§ 07 · SUPPLIER
PEAK LAB
PEPTIDES
SUPPLIER OF RECORD · 12 BATCHES PASSED

We tried nine suppliers across 2025 and kept picking PEAK LAB for LL-37: 99.4% HPLC purity, COA on every batch, cold chain intact. Shop through our link and we earn a small commission — affiliate relationship is disclosed.

Visit PEAK LAB ↗
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