PreclinicalAntimicrobialResearch chemical

LL-37

The body's only human cathelicidin · a 37-amino-acid antimicrobial peptide of innate immunity

Overview

LL-37 is a 37-amino-acid antimicrobial peptide your own immune system produces, the only human cathelicidin. It has broad-spectrum antimicrobial and immunomodulatory activity in the lab and a small number of early-stage human wound-healing trials, but no approved therapeutic anywhere, and signals in cancer biology cut both ways.

01 What is LL-37?

In plain English.

LL-37 is a small antimicrobial peptide that your own body makes. It is the only cathelicidin humans produce, a family of innate-immune peptides shared across mammals. Neutrophils, skin keratinocytes, and the cells lining your airways and gut all secrete LL-37 (or its precursor, hCAP-18) as part of the first-line defence against bacteria, viruses and fungi. The name simply comes from its sequence, it starts with two leucines (LL) and is 37 amino acids long.

⏱ Half-life
Short (minutes, in serum)
☉ Route
Topical / injectable (research)
⚖ Evidence
Preclinical + early trials
📚 Studies
7 referenced

Synthetic LL-37, sold by research-peptide vendors and increasingly visible in biohacker circles, is a lab-made copy of the same molecule. It is not an approved medicine in any jurisdiction. The fact that the body makes LL-37 naturally does not mean injecting more of it is safe, endogenous antimicrobial peptides also play roles in inflammation and cancer biology that get messier the more of them you add.

02 How it works

The simple version, then the science.

LL-37 punches holes in microbial membranes, its positive charge sticks to the negatively charged outside of bacterial cells, then the peptide inserts itself into the membrane and disrupts it. That makes LL-37 broadly active against bacteria (including some antibiotic-resistant strains), some viruses and fungi. Separately, LL-37 acts as a signalling molecule to the immune system: it recruits white blood cells, modulates inflammation, and influences how skin and other tissues heal after injury.

Go deeper · the proposed mechanism

LL-37 is the active C-terminal fragment of hCAP-18, the protein product of the CAMP gene, cleaved out by proteases such as proteinase 3. As an amphipathic α-helical cationic peptide, it disrupts bacterial membranes via the carpet/toroidal-pore model. Beyond direct antimicrobial action it engages receptors including FPR2, P2X7 and EGFR, and modulates TLR signalling, driving chemotaxis of neutrophils, monocytes and T cells, promoting angiogenesis and re-epithelialisation, and altering cytokine output. Vitamin D upregulates CAMP transcription, which is part of why low vitamin D status has been linked to impaired innate immunity. LL-37 is also a known autoantigen in psoriasis and is overexpressed in some chronic inflammatory skin conditions, where its immunomodulatory effects appear to drive, not just respond to, pathology.

03 What it's used for

Each use graded by how strong the evidence actually is.

  • Preclinical
    Broad-spectrum antimicrobial activityRobust in vitro and animal data against gram-positive and gram-negative bacteria, biofilms, some viruses and fungi. No approved antimicrobial drug based on LL-37 exists.
  • Limited
    Chronic wound healing (venous leg ulcers, diabetic foot ulcers)A small Swedish RCT in hard-to-heal venous leg ulcers (Grönberg et al., 2014) reported faster healing with topical LL-37; a 2021 follow-up multicentric RCT was less clear-cut. A 2023 RCT of an LL-37 cream in diabetic foot ulcers reported enhanced healing. All small, none with regulatory approval.
  • Preclinical
    Immune modulation in inflammatory skin diseaseStudied in atopic dermatitis, psoriasis and rosacea biology, where LL-37 expression is altered. Therapeutic role is mechanistic, not established as a treatment.
  • Anecdotal
    Longevity / biohacker antimicrobial protocolsPromoted online as an "immune booster" or chronic-infection adjunct. No human evidence supports general supplementation in healthy adults.
Endogenous does not mean safe to inject more of. LL-37 is a real immune molecule, but it also drives inflammation in psoriasis and rosacea, and shows opposite effects across different cancers (see Safety). Treat "your body already makes it" as a starting point, not reassurance.

04 What the evidence says

The case for LL-37 as biology is strong, thousands of papers describe its structure, antimicrobial mechanism and immunomodulatory roles, and several review articles map the field comprehensively. The case for LL-37 as a medicine is much thinner. A handful of small randomised trials in chronic wounds (hardest-to-heal venous leg ulcers and diabetic foot ulcers) have reported benefit, with mixed consistency between studies and no approved product to date. The clinical-development history of LL-37 and related cathelicidins (and of derived "innate defence regulator" peptides such as IDR-1018) is one of recurrent promise and slow translation: antimicrobial peptide drugs have repeatedly failed late-stage trials elsewhere in the field. The cancer literature is genuinely conflicted, LL-37 has been reported as pro-tumour in breast and ovarian cancers and anti-tumour in colon and gastric cancers, depending on receptor context and tissue. Honest read: real biology, modest early human signal in chronic wounds, unresolved cancer signal, no approved therapeutic.

05 Dosing & administration

Reported in the literature, information not advice.

Because there is no approved human protocol outside of investigational trials, no safe or effective dose has been established for general use. Published clinical work in venous leg ulcers used topical LL-37 in low microgram-per-millilitre concentrations applied to the wound under occlusion in a controlled trial setting. Online research-chemical communities describe subcutaneous injection of milligram-range doses, but these regimens are not supported by clinical evidence and the purity of vendor-supplied LL-37 is unregulated. A qualified clinician should be consulted before considering any peptide.

06 Side effects & safety

Long-term safety in humans is unknown, published trials of LL-37 are small, short and mostly topical. The mechanistic concerns are real and specific. LL-37 has dual signals in cancer biology: it has been reported to promote tumour growth, invasion and metastasis in breast, ovarian, lung and skin cancers (often via FPR2 / EGFR signalling), and to inhibit tumour growth in some gastric and colon cancer models. The direction depends on the cancer, the receptor context and the dose, and there is no clinical safety data to settle which dominates in any given person. LL-37 also drives inflammation in psoriasis (where it is a known autoantigen), rosacea, and possibly atopic dermatitis flares. Injection-site reactions, immune-stimulation effects and unknown interactions are all plausible. Products sold as "LL-37" are unregulated research chemicals, purity, identity and dose-by-dose consistency are not guaranteed. People with a personal or family history of cancer, inflammatory skin disease, autoimmunity, or who are pregnant, breastfeeding or immunocompromised should be especially cautious.

Dual cancer signal, be honest about this. Published research shows LL-37 promoting tumour progression in some cancers (breast, ovarian) and inhibiting it in others (colon, gastric). No human study has resolved which way it falls in real-world use, and "your body makes it" is not a safety argument.

07 Where to buy (research use only)

Vetted on quality and transparency, not an endorsement to use.

Helix Research Labs4.6
Research-use-only peptides with publicly available certificates of analysis. Quality testing does not address the underlying lack of human safety data for synthetic LL-37.
HPLC & MS verifiedPublished COAsResearch use only
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Apex Compounds4.3
Competitive pricing across a broad range of research compounds. Listed for transparency, not an endorsement for human use.
Third-party testedResearch use only
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Vanta Bio4.5
Specialist supplier with independent lab testing on every batch. Product purity does not change the unresolved cancer-signal question for LL-37.
Independent lab testingResearch use only
View ↗
Disclosure: Pepwyse is not affiliated with these companies and does not earn any commission from these links; they are listed for reference only. These products are sold strictly for laboratory research use only and are not for human consumption.

09 Clinical studies & research

Primary sources. Read the science yourself.

Unique features of human cathelicidin LL-37
BioFactors · 2015 Review
Vandamme et al., a widely cited overview of LL-37 structure, processing from hCAP-18, antimicrobial mechanism, and immunomodulatory functions. Good entry point to the biology. View on PubMed →
LL-37: Cathelicidin-related antimicrobial peptide with pleiotropic activity
Pharmacological Reports · 2016 Review
Comprehensive review of LL-37's antimicrobial, chemotactic, wound-healing and immunomodulatory activities, and its emerging dual role in cancer. A balanced map of the literature. View on PubMed →
Antibiofilm properties of cathelicidin LL-37: an in-depth review
World Journal of Microbiology & Biotechnology · 2023 Review
Synthesises the in-vitro and animal evidence that LL-37 disrupts bacterial biofilms, relevant to chronic-wound and device-infection biology. Preclinical: no approved antibiofilm product. View on PubMed →
Treatment with LL-37 is safe and effective in enhancing healing of hard-to-heal venous leg ulcers: a randomized, placebo-controlled clinical trial
Wound Repair and Regeneration · 2014 Human RCT (small)
Grönberg et al., small Swedish RCT reporting that topical LL-37 enhanced healing of hard-to-heal venous leg ulcers vs placebo. One of the only positive human LL-37 RCTs; small sample, single indication. View on PubMed →
Evaluation of LL-37 in healing of hard-to-heal venous leg ulcers: a multicentric prospective randomized placebo-controlled clinical trial
Wound Repair and Regeneration · 2021 Human RCT
Larger follow-up multicentric RCT. Results less clear-cut than the 2014 trial, illustrates how thin and unsettled the human-evidence base for LL-37 still is. View on PubMed →
Efficacy of LL-37 cream in enhancing healing of diabetic foot ulcer: a randomized double-blind controlled trial
Archives of Dermatological Research · 2023 Human RCT (small)
Small double-blind RCT reporting that topical LL-37 cream improved healing of diabetic foot ulcers vs control. Single-centre, modest sample, early signal, not regulatory approval. View on PubMed →
Roles and Mechanisms of Human Cathelicidin LL-37 in Cancer
Cellular Physiology and Biochemistry · 2018 Review
Lays out the dual cancer signal honestly: LL-37 is reported as pro-tumour in breast, ovarian, lung and skin cancers and as anti-tumour in some gastric and colon cancers, depending on receptor context. The clearest single summary of why "endogenous" is not the same as "safe to add more of". View on PubMed →

10 Frequently asked questions

Is LL-37 made by the body?
Yes. LL-37 is the only human cathelicidin, your neutrophils, skin keratinocytes and the epithelial cells lining your airways and gut produce it as part of innate immunity. The version sold by research-peptide vendors is a synthetic copy of the same molecule. Endogenous origin does not by itself make injecting more of it safe.
Are there any human trials of LL-37?
Yes, but few and small. Two randomised placebo-controlled trials in Sweden tested topical LL-37 in hard-to-heal venous leg ulcers (Grönberg et al., 2014 and 2021), with mixed results. A 2023 RCT reported improved diabetic-foot-ulcer healing with topical LL-37 cream. No LL-37 product is approved as a medicine anywhere.
Does LL-37 cause cancer?
It is more complicated than that, and worth being honest about. The published literature shows LL-37 promoting tumour growth and metastasis in some cancers (breast, ovarian, lung, skin) and inhibiting it in others (colon, some gastric models). Direction depends on the cancer type, receptor context and dose, and no human study has resolved which way it falls in practice. That is a meaningful reason for caution, especially in anyone with personal or family cancer history.
Is LL-37 approved by any regulator?
No. LL-37 is not approved as a medicine in the UK, US, EU, Australia or Canada. It is sold only as a research chemical, not for human consumption.
Is LL-37 banned in sport?
LL-37 is not named on the current WADA Prohibited List and is not a recognised performance-enhancing substance. Athletes in tested sport should still consult their anti-doping authority before using any unapproved peptide.
Is LL-37 safe?
Unknown. Published human trials are small and mostly topical. Specific mechanistic concerns include opposite signals in different cancers, a known role in driving inflammation in psoriasis and rosacea, and unregulated purity of vendor-supplied material. People with a personal or family history of cancer, inflammatory skin disease or autoimmunity should be especially cautious.
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