Library / Immunology / LL-37
Evidence: Controlled trialsNot FDA-approvedImmunity

LL-37

Human antimicrobial host-defense peptide produced from hCAP18.

37Amino acids
~4,493Daltons
Varies by formFormula
1995Research period
LL-37Illustrative conformer; drag to rotate.
CNO
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Prepared with AI-assisted drafting and editorial source checking. Author and clarity-review credits are not independent scientific review. No college credit, professional certification or university endorsement is implied. How scientific review will be recorded.

Overview

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In plain language

LL-37 is a 37-amino-acid fragment of the human cathelicidin precursor hCAP18. It participates in host defense, with both antimicrobial and immune-modulating actions; those biological roles do not by themselves establish a treatment. (Morizane & Gallo, 2012)

A laboratory study found reduced bacterial biofilm formation. A separate randomized human wound trial found no statistically significant overall healing improvement. These studies asked different questions. (Overhage et al., 2008) (Mahlapuu et al., 2021)

Molecular values are approximate reference specifications for the named form, not product-specific assay results. Confirm sequence, termini, counterions and modification state against primary chemical records before publication.

Molecular identity

Amino acids
37
Molecular weight
~4,493 Da
Formula
Form-dependent; verify
Sequence
LLGDFFRKSKEKIGKEFKRIVQRIKDFLRNLVPRTES

Sequence map

HydrophobicPolarPositiveNegativeGly / Pro

Hydropathy

Kyte–Doolittle score per residue. Positive values are water-repelling.

Form clarification: Molecular mass depends on sequence and terminal form. Molecular weight is a reference value, not a certificate of analysis.

Origin and history

Agerberth and colleagues reported the human precursor research under the name FALL-39 in 1995. The mature LL-37/hCAP18 system was subsequently studied in host defense, inflammation, laboratory biofilms and wound healing; these are distinct research contexts. (Agerberth et al., 1995) (Morizane & Gallo, 2012)

The 2008 biofilm experiment and the 2021 randomized wound trial illustrate why a laboratory mechanism should not be presented as proof of clinical success. (Overhage et al., 2008) (Mahlapuu et al., 2021)

Human evidence

PreclinicalEarly humanControlled trialsApproved use

The randomized 2021 trial did not show statistically significant healing improvement in the full population. Its exploratory larger-ulcer subgroup does not establish efficacy. The evidence category records a controlled trial, including a null trial, rather than confirmed patient benefit. (Mahlapuu et al., 2021)

Explore the free LL-37 case study to compare that result with the separate in-vitro biofilm experiment. (Overhage et al., 2008)

Safety and regulatory status

See every compound on the regulatory tracker.

Not FDA-approved as a therapeutic LL-37 peptide.

Long-term risks, formulation differences, and human safety evidence require careful review. Educational content only; not medical advice.

Editorial update · November 9, 2026

Changed the evidence category from Early human to Controlled trials to reflect the randomized wound trial, not a finding of proven benefit. Added its overall null result, separated exploratory subgroup findings, and clarified precursor processing and the research date.

Sources

  1. Mahlapuu et al., 2021https://pmc.ncbi.nlm.nih.gov/articles/PMC9298190/
  2. Overhage et al., 2008https://pubmed.ncbi.nlm.nih.gov/18591225/
  3. Morizane & Gallo, 2012https://pmc.ncbi.nlm.nih.gov/articles/PMC3527011/
  4. Agerberth et al., 1995http://www.ncbi.nlm.nih.gov/pmc/articles/PMC42844
Cite this page

Hernandez Gener, E. (2026, November 9). LL-37: molecular data, research history and evidence. VALREXA Biosciences. https://valrexa.com/peptides/ll-37.html

APA style · Editorially updated November 9, 2026 · Our editorial standards

Editorially updated November 9, 2026. Trial and regulatory status can change; confirm in the linked registries. This profile is educational and is not medical advice, a treatment recommendation, or dosing or sourcing guidance. Report an error · Corrections policy

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