Department of Oncology and Diagnostic Sciences, Dental School, University of Maryland, Baltimore, Maryland, USA.
Department of Chemical and Biomolecular Engineering, University of Maryland, College Park, Maryland, USA.
Antimicrob Agents Chemother. 2019 Sep 23;63(10). doi: 10.1128/AAC.00888-19. Print 2019 Oct.
Oral candidiasis (OC) caused by the fungal pathogen is the most common opportunistic infection in immunocompromised populations. The dramatic increase in resistance to common antifungal agents has emphasized the importance of identifying alternative therapeutic options. Antimicrobial peptides have emerged as promising drug candidates due to their antimicrobial properties; specifically, histatin-5 (Hst-5), a peptide naturally produced and secreted by human salivary glands, has demonstrated potent activity against However, as we previously demonstrated vulnerability for Hst-5 to proteolysis by proteolytic enzymes at specific amino acid residues, a new variant (K11R-K17R) was designed with amino acid substitutions at the identified cleavage sites. The new resistant peptide demonstrated no cytotoxicity to erythrocytes or human oral keratinocytes. To evaluate the potential of the new peptide for clinical application, we utilized our FDA-approved polymer-based bioadhesive hydrogel as a delivery system and developed a therapeutic formulation specifically designed for oral topical application. The new formulation was demonstrated to be effective against strains resistant to the traditional antifungals, and the therapeutic efficacy was found to be comparable to that of the common topical antifungal agents in clinical use. Importantly, in addition to its antifungal properties, our findings also demonstrated that the new peptide variant induces cell proliferation and rapid cell migration of human oral keratinocytes, indicative of wound healing properties. The findings from this study support the progression of the novel formulation as a therapeutic agent against oral candidiasis, as well as a therapeutic modality for promoting wound healing.
口腔念珠菌病(OC)由真菌病原体引起,是免疫功能低下人群中最常见的机会性感染。常见抗真菌药物的耐药性急剧增加,这强调了寻找替代治疗方法的重要性。由于具有抗菌特性,抗菌肽已成为有前途的药物候选物;具体而言,人唾液腺天然产生和分泌的肽Histatin-5(Hst-5)对 表现出强大的活性。然而,正如我们之前所证明的,Hst-5 易受 蛋白酶在特定氨基酸残基处的蛋白水解,因此设计了具有在鉴定的切割位点处氨基酸取代的新变体(K11R-K17R)。新的抗性肽对红细胞或人口腔角质形成细胞没有细胞毒性。为了评估新肽用于临床应用的潜力,我们利用我们获得 FDA 批准的聚合物基生物粘附水凝胶作为递送系统,并开发了专门设计用于口腔局部应用的治疗配方。新配方被证明对传统抗真菌药物耐药的 菌株有效,并且治疗效果被发现与临床使用的常见局部抗真菌药物相当。重要的是,除了其抗真菌特性外,我们的研究结果还表明,新的肽变体诱导人口腔角质形成细胞的增殖和快速细胞迁移,表明具有伤口愈合特性。这项研究的结果支持将新型制剂作为治疗口腔念珠菌病的治疗剂以及促进伤口愈合的治疗方式的进展。