PubMed
LL-37, the only human member of the cathelicidin family of antimicrobial peptides
Vandamme et al., 2012
Cathelicidin hCAP18
LL-37 is the only cathelicidin antimicrobial peptide expressed in humans, derived from cleavage of the C-terminus of hCAP18. It demonstrates broad-spectrum antimicrobial activity against bacteria (including MRSA), fungi, and viruses, and also plays critical roles in wound healing, immune modulation, and anti-tumor activity. Expressed primarily in neutrophils, epithelial cells, and skin. Research only.
Overall check-ins
Trackers & reports
Overview
LL-37 is the only cathelicidin antimicrobial peptide expressed in humans, derived from cleavage of the C-terminus of hCAP18. It demonstrates broad-spectrum antimicrobial activity against bacteria (including MRSA), fungi, and viruses, and also plays critical roles in wound healing, immune modulation, and anti-tumor activity. Expressed primarily in neutrophils, epithelial cells, and skin. Research only.
Community
From check-in ratings — separate from side effects logged below. Side effects are logged separately from overall experience. A favorable check-in can still include nausea, fatigue, or injection-site reactions.
Favorable 100% · Mixed 0% · Unfavorable overall 0%
Benefits users selected when logging a favorable or mixed check-in.
Median bucket: 100–200 mcg · Most common: 100–200 mcg
Reports span 100–400 mcg
Anonymized self-reports from PeptIQ users — not prescribing guidance. Buckets group similar logged amounts; open-ended top buckets mean “at least” that dose.
Research
PubMed
Vandamme et al., 2012
PubMed
Dean et al., 2011
ClinicalTrials.gov
ClinicalTrials.gov, 2024
PubMed
Geng et al., 2024
PubMed
Soman et al., 2026
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This page summarizes 6 anonymized self-reports from PeptIQ users who track LL-37, including commonly reported effects and co-tracked peptides. These are observational patterns, not clinical outcomes.
PeptIQ separates overall check-in ratings (favorable, mixed, or unfavorable) from logged side effects like nausea or fatigue. Users often report benefits and side effects in the same check-in — a high experience score does not mean zero side effects were noted.
5 sources are linked on this page, including PubMed articles, clinical trial registries, and FDA labels where applicable. Citations describe published research — not recommendations.
This wiki does not assess safety or recommend use. LL-37 is listed as Research Only. Consult a licensed clinician for personal medical decisions.
Research, primarily in animal models, suggests LL-37 may have a wide range of therapeutic potentials due to its ability to promote angiogenesis (formation of new blood vessels), stimulate collagen synthesis, and modulate inflammatory responses.
SourceLL-37 is not approved by the FDA for any human use. There is no legal basis for selling it as a drug, food, or dietary supplement in the United States. The FDA has classified LL-37 as a Category 2 bulk drug substance, which explicitly prohibits licensed compounding pharmacies from using it in compounded medications.
SourceThe safety and effectiveness of LL-37 have not been thoroughly evaluated in humans through rigorous clinical trials. This lack of human data means that safe dosages, short-term side effects, and long-term health consequences are largely unknown.
SourceWhile there are over 200 published studies on LL-37, the vast majority are animal or in vitro (cell) studies. These preclinical studies consistently show positive results across various tissue types. However, there is a significant lack of comprehensive human clinical trial data.
Source