Antimicrobial Peptides (AMPs): A Breakthrough Approach for Wound Healing and Infection Control
摘要
Chronic wounds, such as diabetic ulcers, pressure sores, and burns, remain a global healthcare burden due to the rising threat of antibiotic-resistant infections and impaired healing processes. Traditional antibiotics are losing efficacy, but antimicrobial peptides (AMPs), part of the innate immune system, offer a revolutionary solution.
PurposeThis review analyzes 34 potent AMPs with dual antimicrobial and wound-healing properties, highlighting their mechanisms, efficacy, and clinical potential.
ResultsAMPs disrupt microbial membranes via pore formation (e.g., Magainin 2, Myxidin, Lucifensin), cell wall inhibition (e.g., Nisin, Plectasin), and intracellular interference (e.g., PR-39 inhibits DNA replication). Notably, these peptides target multi-drug resistant strains like MRSA (Temporin A, Indolicidin) and P. aeruginosa (Esculentin-1a, Cathelicidin-DM). Beyond killing microbes, AMPs actively promote wound healing through angiogenesis (LL-37, Epinecidin-1), keratinocyte proliferation (Temporin A, hBD-2), collagen synthesis (LL-37, Esculentin-1a), and anti-inflammatory modulation (AW1, Chensinin-1b). Despite their promise, challenges such as salt sensitivity (hBD-2), potential cytotoxicity (MSI-78), and resistance development (S. aureus to LL-37) persist. To overcome these limitations, researchers are exploring structural engineering (non-natural amino acids), advanced delivery systems (hydrogels for Kn2-7, TS-CATH), and synergistic combinations (Bactenecin + IDR-1018). Remarkably, some AMPs like Cathelicidin-NV promote wound healing without direct antimicrobial activity, while S100A12 uses "nutritional immunity" (Zn2⁺ sequestration) to inhibit H. pylori.
ConclusionIn conclusion, AMPs represent a transformative frontier in wound care, combining broad-spectrum antimicrobial activity, immunomodulation, and tissue regeneration. Further research into optimized delivery and clinical trials will unlock their full potential as next-generation therapeutics.
Graphical Abstract