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Fungal-targeted nanoconstructs (FTNx), using antisense oligonucleotides against FKS1 and CHS3 , can inhibit fungal cell wall synthesis genes, reduce fungal burden and improve survival in murine candidiasis models, exhibit broad-spectrum antifungal activity, including against clinical isolates of Candida auris ( Li et al., 2025a)

KPV, by contrast, is a short tripeptide fragment derived from the alpha-melanocyte stimulating hormone sequence that retains key signaling properties of the parent melanocortin peptide, allowing researchers to investigate inflammatory signaling pathways and epithelial barrier biology in controlled laboratory systems

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Available from: Rinaldi A, Caraffi R, Grazioli MV, Oddone N, Giardino L, Tosi G, et al