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Research compoundImmune & Specialty Research

LL-37

Also known as: Cathelicidin

LL-37 is a 37-amino-acid peptide and the only member of the cathelicidin antimicrobial-peptide family made by humans. Research includes extensive cell and biophysical work, mouse studies and a few small human trials.

Evidence: limited · Mostly lab and mouse studies; small human trials

At a glance

Class
Human cathelicidin antimicrobial peptide
Developer
No pharmaceutical developer for this research compound
FDA status
Not FDA-approved
Human data
Small randomized human studies (see publications)
Animal / lab data
Bacterial, cell and membrane studies; mouse wound and skin-inflammation models

Where it’s been studied

123
  • 1SkinWound model, mice (2021); skin-inflammation model, mice (2025)
  • 2Innate immune systemMacrophage and neutrophil studies reviewed (2024, 2025)
  • 3Bacterial membranesBiophysical and structural studies reviewed (2024)

Mechanism studied

LL-37 is established as a cationic, helix-forming peptide that binds negatively charged bacterial membranes and molecules such as LPS and lipoteichoic acid, disrupting membranes in lab studies [1][2]. Reviews also describe immune-signaling roles: attracting immune cells, inducing autophagy in macrophages and changing neutrophil behavior in mouse studies [1][2]. These signaling roles are context-dependent; in mice, repeated LL-37 injection is itself used to create a skin-inflammation model [5].

What the research shows

StudyModelReported resultSource
Mouse wound model with MRSA [3]Mouse
Back-skin wound model in BALB/c mice inoculated with S. aureus (MRSA); LL-37 vs teicoplanin, topical and/or systemic
Combined topical plus systemic LL-37 group showed more re-epithelialization, granulation tissue, collagen organization and new vessel formation on histologyPeer-reviewed
Antibiotics 2021
Topical cream trial [4]Human
25 adults, randomized 1:1, double-blind, placebo-controlled topical study, 4 weeks
Primary efficacy measure: granulation index. PublishedPeer-reviewed
Arch Dermatol Res 2023
Skin-inflammation model [5]Mouse
Short-term vs long-term LL-37 skin-injection model in mice
Long-term model showed skin thickening, new vessel formation and both innate and adaptive immune activationPeer-reviewed
Anim Models Exp Med 2025
Review of LL-37 and analogs [1]Review
Lab, cell and animal studies of LL-37 and modified fragments (KR-12, FK-16, OP-145 and others)
Summarizes membrane-disruption mechanism, LPS binding and analog designs aimed at stability and selectivityPeer-reviewed
Int J Mol Sci 2025
Structure and activity review [2]Review
Biophysical, structural and functional studies of LL-37
Summarizes structure, antimicrobial activity and immune-signaling roles to guide design of LL-37-based moleculesPeer-reviewed
Biomolecules 2024

Human trials are listed for research context only; outcomes are reported in the linked publications. Animal and lab results do not establish effects in humans.

Not currently stocked

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More in Immune & Specialty Research

Sources

  1. Voronko OE et al. (2025). doi:10.3390/ijms26168103 Source
  2. Bhattacharjya S et al. (2024). doi:10.3390/biom14030320 Source
  3. Simonetti O et al. (2021). doi:10.3390/antibiotics10101210 Source
  4. Miranda E et al. (2023). doi:10.1007/s00403-023-02657-8 Source
  5. Wu Y et al. (2025). doi:10.1002/ame2.70020 Source
For research use only. Not for human or veterinary use. Not a drug, food or cosmetic, and not intended to diagnose, treat, cure or prevent any disease. This library summarizes published research for educational purposes. PureLab Performance Inc.