Department of Oral Immunology and Infectious Diseases, University of Louisville School of Dentistry, Louisville, Kentucky.
Mol Oral Microbiol. 2019 Oct;34(5):169-182. doi: 10.1111/omi.12267. Epub 2019 Aug 15.
The development of the oral biofilm requires a complex series of interactions between host tissues and the colonizing bacteria as well as numerous interspecies interactions between the organisms themselves. Disruption of normal host-microbe homoeostasis in the oral cavity can lead to a dysbiotic microbial community that contributes to caries or periodontal disease. A variety of approaches have been pursued to develop novel potential therapeutics that are active against the oral biofilm and/or target specific oral bacteria. The structure and function of naturally occurring antimicrobial peptides from oral tissues and secretions as well as external sources such as frog skin secretions have been exploited to develop numerous peptide mimetics and small molecule peptidomimetics that show improved antimicrobial activity, increased stability and other desirable characteristics relative to the parent peptides. In addition, a rational and minimalist approach has been developed to design small artificial peptides with amphipathic α-helical properties that exhibit potent antibacterial activity. Furthermore, with an increased understanding of the molecular mechanisms of beneficial and/or antagonistic interspecies interactions that contribute to the formation of the oral biofilm, new potential targets for therapeutic intervention have been identified and both peptide-based and small molecule mimetics have been developed that target these key components. Many of these mimetics have shown promising results in in vitro and pre-clinical testing and the initial clinical evaluation of several novel compounds has demonstrated their utility in humans.
口腔生物膜的形成需要宿主组织与定植细菌之间一系列复杂的相互作用,以及生物体之间大量的种间相互作用。口腔中正常的宿主-微生物平衡被打破会导致微生物群落失调,从而导致龋齿或牙周病。人们已经尝试了多种方法来开发针对口腔生物膜和/或特定口腔细菌的新型潜在治疗药物。人们利用口腔组织和分泌物中天然存在的抗菌肽的结构和功能以及来自青蛙皮肤分泌物等外部来源,开发了许多肽模拟物和小分子肽模拟物,这些模拟物在抗菌活性、稳定性和其他理想特性方面相对于母体肽都有所提高。此外,还开发了一种合理的简约方法来设计具有两亲性α-螺旋特性的人工小肽,这些小肽具有很强的抗菌活性。此外,随着对有助于口腔生物膜形成的有益和/或拮抗种间相互作用的分子机制的认识不断增加,已经确定了新的治疗干预靶点,并开发了针对这些关键成分的基于肽和小分子的模拟物。这些模拟物中的许多在体外和临床前测试中都显示出了有前景的结果,并且几种新型化合物的初步临床评估表明了它们在人类中的实用性。