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.
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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
Positive 100% · Neutral 0% · Negative 0%
Median: 100–200 mcg · Most common: 100–200 mcg
Research
PubMed
Vandamme et al., 2012
PubMed
Dean et al., 2011
Help
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.
2 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