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LL-37

Cathelicidin, hCAP-18, FALL-39, CAP-18

Quick Stats
Studies 2230
Trials 95
Score 2
2025 pubmed 10 citations

Engineered Macrophage Membrane-Camouflaged Nanodecoys Reshape the Infectious Microenvironment for Efficient Periodontitis Treatment.

Lin. Sihan S; Xu. Zeqian Z; Liu. Yulan Y; Yang. Guangzheng G; Qi. Xuanyu X; Huang. Yijia Y; Zhou. Mingliang M; Jiang. Xinquan X

Key Findings

  • LL‑37 attached to a macrophage‑derived membrane helps the nanodecoys specifically target periodontitis‑causing bacteria.
  • The nanodecoys combine an enzyme (LAAO) and hollow manganese dioxide to generate oxygen in low‑oxygen gum tissue, disrupting bacterial metabolism.
  • They activate NRF2 pathways, lower oxidative stress, shift macrophages to a healing mode, and promote bone‑forming cell activity, leading to better alveolar bone regeneration in mice.

Practical Outcomes

  • For now, the work is a proof‑of‑concept that LL‑37 can be delivered in a sophisticated, targeted way to treat gum disease. It doesn’t translate into a DIY protocol or supplement regimen, but it highlights LL‑37’s potential as a powerful oral antimicrobial and anti‑inflammatory agent worth watching as the technology matures.

Summary

Scientists made tiny particles that wear a fake macrophage skin and carry the natural antimicrobial peptide LL‑37. These particles can stick to harmful mouth bacteria, produce oxygen to help kill them, calm down inflammation, and support bone healing in gum disease. The study shows the concept works in animals, but the technology is still far from something you can buy or DIY.

Abstract

A vicious cycle between microbiota dysbiosis and hyperactivated inflammation, hardly disrupted by conventional therapies, remains a significant clinical challenge for periodontitis treatment. Herein, by cloaking a cascade catalysis system in an engineered macrophage membrane, a nanodecoy-based strategy, with targeted bacteria-killing and immunomodulatory abilities, is proposed for reshaping the hostile periodontitis microenvironment. Specifically, recombinant human antimicrobial peptide, LL-37, is anchored to a Toll-like receptor-enriched macrophage membrane via genetic engineering, which facilitates the specific bacteria elimination and efficient tissue retention of the nanodecoys. Moreover, the cascade catalysis system integrates L-amino acid oxidase (LAAO) with hollowed manganese dioxide (hMnO<sub>2</sub>) by reciprocal elevation of the catalytic efficiency of hMnO<sub>2</sub> and LAAO, leading to accelerated O<sub>2</sub> generation under a hypoxic microenvironment and disrupted metabolism of periodontopathogenic bacteria. Notably, the nanodecoys trigger the nuclear translocation of NF-E2-related factor-2 (NRF2) to reduce oxidative stress response and rewire the polarization of macrophages, thereby boosting the osteogenic differentiation of osteoblasts. Furthermore, the alveolar bone regeneration therapeutically benefits from the nanodecoys in vivo. Altogether, these results highlight the attractive functions of engineered macrophage membrane-cloaked nanodecoys for effective periodontitis treatment.

Study Information

Provider

pubmed

Year

2025

Date

2025-04-14T00:00:00.000Z

DOI

10.1021/acsnano.4c14305

Citations

10

References

78