LL-37 / Cathelicidin
aka Cathelicidin
LL-37 / Cathelicidin in brief
LL-37 / Cathelicidin is the only known human cathelicidin, an antimicrobial peptide with broad immune functions. Amino Axiom rates its evidence base strong, drawing on 13 PubMed results (8 human studies) and 20 registered trials listed below. Its reported half-life is ~1 hour (preclinical). It is filed under Immune & Inflammation in the Amino Axiom compound index.
Research data
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Long-form breakdowns
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Overview
LL-37 is the C-terminal peptide derived from the human cathelicidin antimicrobial protein (hCAP18). It is the only known human cathelicidin and has broad-spectrum antimicrobial activity. It also modulates immune responses and has been implicated in various inflammatory diseases.
PubMed results: 13 · Human studies: 8 · Animal studies: 10
Dosing Ranges
Ranges reflect protocols studied in published research and animal-model extrapolation. Presented for research purposes only, not a recommendation or instruction for human use.
- Topical — standard range Various formulations
Half-Life
~1 hour (preclinical) (low confidence)
Observed Benefits
- Broad-spectrum antimicrobial activity (Strong preclinical): LL-37, the only human cathelicidin peptide, has demonstrated bactericidal and antiviral activity in vitro and in animal infection models via membrane disruption and immune modulation.
- Innate immune modulation (Moderate clinical): Human and translational studies link LL-37 expression to host defense and inflammation, including research contexts involving vitamin D status, periodontitis, rosacea, and sepsis biology.
- Wound and barrier defense research (Strong preclinical): Preclinical work has examined LL-37 for effects on epithelial repair, chemotaxis, and angiogenesis pathways relevant to barrier tissues.
Side Effects
- Pro-inflammatory or cytotoxic effects at high local concentrations — Moderate, Not established. In vitro and animal data show that high LL-37 concentrations can be cytotoxic and amplify inflammatory signaling; human dosing safety for exogenous peptide is not well established.
- Local irritation in experimental delivery — Mild, Anecdotal. Local tissue irritation has been noted in early experimental delivery contexts; formal frequency data in controlled trials remain limited.
Contraindications
- Active inflammatory skin disease under uncontrolled study conditions (Theoretical / Preclinical): LL-37 is elevated in several inflammatory dermatoses (e.g., rosacea pathways); exogenous peptide could theoretically worsen dysregulated innate responses.
- Known hypersensitivity to cationic antimicrobial peptides (Theoretical / Preclinical): Peptide membrane activity and immune adjuvancy create theoretical risk of severe local or systemic reaction in susceptible research subjects.
Storage
Lyophilized (powder): Frozen (-20°C), Up to 24 months. Light sensitive: yes, store dark
Reconstituted (solution): Refrigerated (2-8°C), 4-6 weeks. Solvent: Bacteriostatic water
Clinical Trials
- NCT02930434 — Effects of Antarctic Environment on Vitamin D Status and Health Risk Biomarkers of Its Inhabitants (NA), status: COMPLETED. Indications: Vitamin D Deficiency
- NCT07490587 — To Investigate the Effects of Bifidobacterium Animalis Subsp. Lactis XLTG11 on Growth and Development, Incidence of Allergy and Immune Function in Infants (PHASE2), status: RECRUITING. Indications: Healthy Children
- NCT03923218 — Effects of Smoking and Vitamin D3 on the Levels of Human Cathelicidin Peptide LL-37, status: COMPLETED. Indications: Periodontitis
- NCT01398280 — Effects of Aminocaproic Acid (ACA) on Rosacea-specific Inflammation (EARLY_PHASE1), status: COMPLETED. Indications: Rosacea
- NCT00788320 — Vitamin D in Active Tuberculosis (TB) Study (NA), status: WITHDRAWN. Indications: Tuberculosis
- NCT01689441 — Randomized Controlled Trial of Calcitriol vs. Placebo Among Critically-ill Patients With Sepsis (PHASE2), status: COMPLETED. Indications: Severe Sepsis or Septic Shock
- NCT01372995 — Vitamin D in Ventilated ICU Patients (PHASE2), status: COMPLETED. Indications: Respiratory Failure
- NCT02138591 — Therapeutic Benefit of Preoperative Supplemental Vitamin D in Patients Undergoing Major Surgical Procedures. (PHASE3), status: WITHDRAWN. Indications: Vitamin d Deficiency
- NCT02945683 — Effects of Lactobacillus Reuteri Plus Vitamin D3 in Children With Atopic Dermatitis (NA), status: COMPLETED. Indications: Atopic Dermatitis
- NCT00407979 — Comparison of Cathelicidin Expression in Skin and Saliva in Patients With Atopic Dermatitis and Psoriasis, status: COMPLETED. Indications: Atopic Dermatitis, Psoriasis
- NCT02278172 — The Effects of Vitamin D Supplementation on Aerobic Fitness in Athletes (PHASE4), status: COMPLETED. Indications: Aerobic Fitness (VO2max)
- NCT06867250 — Peri-implant Vitamin D and Cathelicidin (LL-37) Levels, status: COMPLETED. Indications: Peri-Implantitis and Peri-implant Mucositis
- NCT05094570 — Interleukin-4Ra Blockade by Dupilumab Decreases Staphylococcus Colonization and Increases Microbial Diversity in CRSwNP (PHASE4), status: RECRUITING. Indications: Nasal Polyps, Staphylococcus Aureus
- NCT06552364 — Air Pollution and Inhaled Corticosteroids in COPD (PHASE4), status: NOT_YET_RECRUITING. Indications: COPD
- NCT01026363 — hCAP18 Levels and Vitamin D Deficiency in Chronic Kidney Disease (NA), status: WITHDRAWN. Indications: Chronic Kidney Disease, Vitamin D Deficiency
- NCT01758081 — Effects of Vitamin D and Omega-3 Fatty Acids on Infectious Diseases and hCAP18 (VITAL Infection) (NA), status: ACTIVE_NOT_RECRUITING. Indications: Infections, Human Cathelicidin Antimicrobial Peptide (hCAP-18)
- NCT05244018 — Outcome of High Dose Vitamin D on Prognosis of Sepsis Requiring Mechanical Ventilation (PHASE4), status: COMPLETED. Indications: Sepsis
- NCT07280754 — Evaluation of 25(OH)D3 and LL-37 Levels in Periimplant Sulcus Fluid, status: NOT_YET_RECRUITING. Indications: Peri Implantitis, Peri Implant Mucositis
- NCT02178488 — Efficacy Study of Vitamin D Supplementation to Meticillin Resistant Staphylococcus Aureus (MRSA) Carriers (PHASE2), status: COMPLETED. Indications: Methicillin Resistant Staphylococcus Aureus, Vitamin D3 Deficiency
- NCT05969275 — Umbilical Mesenchymal Stromal Cells as Cellular Immunotherapy for Septic Shock (PHASE2), status: RECRUITING. Indications: Septic Shock, Sepsis, Pathologic Processes, Shock, Systemic Inflammatory Response Syndrome, Inflammation, Infections