Reynolds Eric C, O'Brien-Simpson Neil, Rowe Tony, Nash Andrew, McCluskey Jackie, Vingadassalom Didier, Kleanthous Harold
Melbourne Dental School, Oral Health CRC, Melbourne, Australia.
CSL Ltd, Melbourne, Australia.
J Oral Microbiol. 2015 Sep 18;7:29125. doi: 10.3402/jom.v7.29125. eCollection 2015.
Chronic periodontitis is an inflammatory disease of the supporting tissues of the teeth associated with a polymicrobial biofilm (subgingival plaque) accreted to the tooth which results in destruction of the tooth's supporting tissues. A characteristic feature of the disease-associated plaque is the emergence of proteolytic species. One of these species, Porphyromonas gingivalis has recently been described as a keystone pathogen as it dysregulates the host immune response to favour the polymicrobial biofilm disrupting homeostasis to cause dysbiosis and disease. The level of P. gingivalis in subgingival plaque above threshold levels (~10% of total bacterial cell load) has been demonstrated to predict imminent clinical attachment loss (disease progression) in humans. Porphyromonas gingivalis is found as microcolonies in the superficial layers of subgingival plaque adjacent to the periodontal pocket epithelium which helps explain the strong association with underlying tissue inflammation and disease at relatively low proportions (10%) of the total bacterial cell load of the plaque. The mouse periodontitis model has been used to show that inflammation is essential to allow establishment of P. gingivalis at the levels in plaque (10% or greater of total bacterial cell load) necessary to produce dysbiosis and disease. The extracellular proteinases "gingipains" (RgpA/B and Kgp) of P. gingivalis have been implicated as major virulence factors that are critical for dysbiosis and disease. This has resulted in the strategy of targeting the gingipains by vaccination. We have produced a recombinant immunogen which induces an immune response in mice that neutralises the proteolytic and host/bacterial binding functions of the gingipains. Using this immunogen as a therapeutic vaccine in mice already infected with P. gingivalis, we have shown that inflammation and alveolar bone loss can be substantially reduced. The protection was characterised by a predominant Th2 cytokine and antibody (IgG1) response and shown to be mediated by the gingipain neutralising antibodies using adoptive transfer and systemic/topical passive antibody experiments. Vaccination may be a useful adjunct to scaling and root planing in the treatment of P. gingivalis-mediated chronic periodontitis.
慢性牙周炎是一种牙齿支持组织的炎症性疾病,与附着在牙齿上的多微生物生物膜(龈下菌斑)有关,该生物膜会导致牙齿支持组织的破坏。与疾病相关的菌斑的一个特征是蛋白水解菌的出现。其中一种菌,牙龈卟啉单胞菌,最近被描述为关键病原体,因为它会失调宿主免疫反应,以利于多微生物生物膜破坏体内平衡,导致生态失调和疾病。龈下菌斑中牙龈卟啉单胞菌的水平高于阈值水平(约占细菌细胞总数的10%)已被证明可预测人类即将发生的临床附着丧失(疾病进展)。牙龈卟啉单胞菌以微菌落的形式存在于与牙周袋上皮相邻的龈下菌斑表层,这有助于解释在菌斑细菌细胞总数相对较低比例(10%)时,它与潜在组织炎症和疾病的强关联。小鼠牙周炎模型已被用于表明炎症对于牙龈卟啉单胞菌在菌斑中达到产生生态失调和疾病所需的水平(占细菌细胞总数的10%或更高)至关重要。牙龈卟啉单胞菌的细胞外蛋白酶“牙龈蛋白酶”(RgpA/B和Kgp)被认为是对生态失调和疾病至关重要的主要毒力因子。这导致了通过疫苗接种靶向牙龈蛋白酶的策略。我们已经制备了一种重组免疫原,它能在小鼠体内诱导免疫反应,中和牙龈蛋白酶的蛋白水解和宿主/细菌结合功能。在已经感染牙龈卟啉单胞菌的小鼠中使用这种免疫原作为治疗性疫苗,我们已经表明炎症和牙槽骨丧失可以显著减少。这种保护的特征是主要由Th2细胞因子和抗体(IgG1)反应介导,并且通过过继转移和全身/局部被动抗体实验表明是由牙龈蛋白酶中和抗体介导的。疫苗接种可能是治疗牙龈卟啉单胞菌介导的慢性牙周炎时龈上洁治和根面平整的有用辅助手段。