Peptides DB
Research-centric peptide and protocol reference hub
Study 24 of 35LL-37 literaturebiorxiv-preprint · Meta-analysis2026

<em>In Vivo</em> Efficacy of LL-37 and Its Derivative Peptides Against Methicillin-Resistant <em>Staphylococcus aureus</em> in Animal Models: A Systematic Review and Meta-Analysis

LL-37 and its derivatives show significant antibacterial activity and improved wound healing in MRSA-infected animal models, but caution is warranted in translating these findings to human applications.

Read at biorxiv-preprintAdd to compare

Where it sits

this study against the rest of the ll-37 corpus
6
Preclinical
20
Observational
0
Open-label
5
Randomised
4
Reviews · this one

Summary and findings

This study evaluated the antibacterial efficacy of LL-37 and its derivatives against methicillin-resistant Staphylococcus aureus (MRSA) in animal models. The meta-analysis included 23 studies, with four providing sufficient data for analysis. LL-37 showed significant improvements in bacterial clearance and wound healing compared to controls.

How much of this paper we could read: full text read (0.80). We had a clear abstract, so the summary below closely tracks the paper. What this means →
-7.86 standardized mean difference in bacterial eradication vs controls, 95% CI: -9.40 to -6.33, P < 0.001, n=44.2026

Abstract

The authors’ words, as biorxiv-preprint supplied them

<h4>Objectives: </h4> Methicillin-resistant Staphylococcus aureus (MRSA) is a major global pathogen with increasing resistance to conventional antibiotics. LL-37 and its derivative peptides have shown promising in vivo antibacterial activity. This study evaluated whether these peptides improve bacterial clearance, wound healing, and survival compared with controls in animal models of MRSA infection. <h4>Methods:</h4> The literature search was last updated on 21 April 2026. A systematic search of PubMed, Scopus, and Embase was conducted to identify preclinical studies assessing the antibacterial activity of LL-37 and its derivatives in MRSA animal infection models. Guided by PRISMA, 1,014 unique records were screened after removing 368 duplicates; 23 studies met the inclusion criteria, and 16 were included in the qualitative synthesis. Four studies (one comprising three independent experiments) provided sufficient data for meta-analysis. Extracted variables included sample size, bacterial counts (mean ± SD), and intervention/control details. Standardized mean differences (Hedges' g) were calculated using a random-effects model, and study quality was assessed using SYRCLE's risk-of-bias tool. <h4>Results:</h4> The meta-analysis of bacterial clearance pooled data from six independent experimental results (n = 44 animals). LL-37 and its derivatives achieved markedly greater bacterial eradication than controls, yielding a pooled standardized mean difference (SMD) of -7.86 (95% CI: -9.40 to -6.33; P &lt; 0.001). All studies favoured LL-37, with no confidence intervals crossing zero. Heterogeneity was negligible (I² = 0%, τ² &lt; 0.0001, P = 0.645), and the prediction interval (-9.74 to -5.99) indicated consistently large effects across similar experimental contexts. For wound healing (binary outcome), pooled analysis showed that LL-37 significantly increased complete wound closure rates compared with controls, with a pooled risk ratio (RR) of 1.25 (95% CI: 1.16-1.36). The pooled proportion of healed wounds was 89.3% in the LL-37 groups versus 70.0% in controls, indicating a clinically relevant improvement. <h4>Conclusions:</h4> LL-37 and its derivative peptides demonstrate robust antibacterial activity and significantly enhance wound healing in MRSA-infected animal models. The large and consistent effects observed across studies support their advancement toward translational research and early-phase clinical trials for potential human therapeutic use.

Background

Not reported in abstract.

Methods

Not reported in abstract.

Results

Not reported in abstract.

Interpretation

Not reported in abstract.

Limitations

Not reported in abstract.

Elsewhere in the LL-37 corpus

CAge-Dependent Effects of Macrophage Derived Cathelicidin Antimicrobial Peptide on Bone Fracture Repairbiorxiv-preprint · 2026 · Not reported in abstract.AnimalCA koala pangenome reveals hidden structural variation with implications for disease and fertilitybiorxiv-preprint · 2026 · n=13 · Approximately 193,000 SVs identified.AnimalCLL-37 and Citrullinated-LL-37 elicited Transcriptome and Cytokine Profiles in Human Bronchial Epithelial Cells: Citrullination dampens the inflammatory biosignaturebiorxiv-preprint · 2026 · Inflammatory response was significantly less (by ∼45%) with citLL-37 compared to LL-37.In vitroCValorisation of invasive North Sea macroalgae as functional feed additives to improve disease resilience in Pacific white shrimp (Litopenaeus vannamei)biorxiv-preprint · 2026 · Survival increased from 60.00 ± 12.02% in the control to 74.44 ± 8.39% in the seaweed-supplemented group.AnimalBAn audit assessing data quality, viral suppression, and transition to dolutegravir among children and adolescents with HIV in care at eThekwini Municipality, South Africabiorxiv-preprint · 2026 · 10% had a last VL ≥1000 copies/mL.HumanDCoarse composition suffices: tabular in-context learning for multi-activity antimicrobial peptide profilingbiorxiv-preprint · 2026 · mAP-5=77.8% on ESCAPE benchmark, n=82,359 peptides.review