Laboratory of Immunology, Department of Translational Physiology, Infectiology and Public Health, Faculty of Veterinary Medicine, Ghent University, Merelbeke, Belgium.
Department of Surgical and Radiological Sciences, School of Veterinary Medicine, University of California, Davis, CA, United States.
Front Immunol. 2021 Dec 2;12:768397. doi: 10.3389/fimmu.2021.768397. eCollection 2021.
Approximately 9 out of 10 adults have some form of periodontal disease, an infection-induced inflammatory disease of the tooth-supporting tissues. The initial form, gingivitis, often remains asymptomatic, but this can evolve into periodontitis, which is typically associated with halitosis, oral pain or discomfort, and tooth loss. Furthermore, periodontitis may contribute to systemic disorders like cardiovascular disease and type 2 diabetes mellitus. Control options remain nonspecific, time-consuming, and costly; largely relying on the removal of dental plaque and calculus by mechanical debridement. However, while dental plaque bacteria trigger periodontal disease, it is the host-specific inflammatory response that acts as main driver of tissue destruction and disease progression. Therefore, periodontal disease control should aim to alter the host's inflammatory response as well as to reduce the bacterial triggers. Vaccines may provide a potent adjunct to mechanical debridement for periodontal disease prevention and treatment. However, the immunopathogenic complexity and polymicrobial aspect of PD appear to complicate the development of periodontal vaccines. Moreover, a successful periodontal vaccine should induce protective immunity in the oral cavity, which proves difficult with traditional vaccination methods. Recent advances in mucosal vaccination may bridge the gap in periodontal vaccine development. In this review, we offer a comprehensive overview of mucosal vaccination strategies to induce protective immunity in the oral cavity for periodontal disease control. Furthermore, we highlight the need for additional research with appropriate and clinically relevant animal models. Finally, we discuss several opportunities in periodontal vaccine development such as multivalency, vaccine formulations, and delivery systems.
大约十分之九的成年人患有某种形式的牙周病,这是一种由感染引起的牙齿支持组织炎症性疾病。最初的形式,牙龈炎,通常没有症状,但这可能发展为牙周炎,通常与口臭、口腔疼痛或不适以及牙齿脱落有关。此外,牙周炎可能导致心血管疾病和 2 型糖尿病等全身疾病。控制选择仍然是非特异性的、耗时的和昂贵的;主要依赖于机械清创术去除牙菌斑和牙石。然而,虽然牙菌斑细菌引发牙周病,但宿主特异性炎症反应是导致组织破坏和疾病进展的主要驱动因素。因此,牙周病的控制应该旨在改变宿主的炎症反应,以及减少细菌触发因素。疫苗可能为机械清创术提供一种有效的辅助手段,用于预防和治疗牙周病。然而,牙周病的免疫发病机制的复杂性和多微生物方面似乎使牙周病疫苗的开发复杂化。此外,成功的牙周病疫苗应该在口腔中诱导保护性免疫,这对于传统的疫苗接种方法来说是困难的。黏膜疫苗接种的最新进展可能会弥合牙周病疫苗开发中的差距。在这篇综述中,我们全面概述了黏膜疫苗接种策略,以诱导口腔中的保护性免疫,从而控制牙周病。此外,我们强调需要使用适当的和具有临床相关性的动物模型进行更多的研究。最后,我们讨论了牙周病疫苗开发中的几个机会,如多价性、疫苗配方和递送系统。