Novel mechanisms and 'complement-ary' therapy in periodontitis

牙周炎的新机制和“补充”疗法

• 批准号: 8216805
• 负责人: Georgios Hajishengallis
• 金额: $ 40万
• 依托单位: UNIVERSITY OF PENNSYLVANIA
• 依托单位国家: 美国
• 财政年份: 2012
• 资助国家: 美国
• 起止时间: 2012-02-01 至 2016-12-31
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/8216805
• 关键词: Address; Adult; Affect; Age; Aging; Alveolar Bone Loss; Animal Model; Area; Atherosclerosis; Attenuated; Bacteria; C5a anaphylatoxin receptor; Cells; Chronic; Clinical; Clinical Trials; Collaborations; Complement; Data; Diabetes Mellitus; Disease; Exudate; Fusobacterium nucleatum; Goals; Health; Host Defense; Human; Immune; Immune response; Immunity; Individual; Infection; Inflammation; Inflammatory; Intervention; Link; Measurement; Mediating; Modeling; Molecular; Mus; Mutation; Nutrient; Pathogenesis; Pathology; Pathway interactions; Patients; Pennsylvania; Periodontal Diseases; Periodontitis; Pharmaceutical Preparations; Porphyromonas gingivalis; Pre-Clinical Model; Receptor Signaling; Recurrent disease; Regulation; Risk; Role; Safety; School Dentistry; Signal Pathway; Staging; Testing; Therapeutic; Therapeutic Intervention; Time; Tissues; Toll-like receptors; Tooth structure; Transgenic Mice; Translations; Universities; base; complement C3 precursor; complement pathway; complement system; immunopathology; inhibitor/antagonist; killings; medical schools; microbial; mouse model; novel; novel therapeutics; pathogen; pre-clinical; prevent; protective effect; research study; therapeutic target; translational approach

DESCRIPTION (provided by applicant): Novel Mechanisms and 'Complement-ary' Therapy in Periodontitis Project Summary Periodontal inflammation affects the majority of adults, while an estimated 10-15% develops severe periodontitis which exerts a systemic impact on the patients (e.g., increased risk for atherosclerosis and diabetes). However, the underlying immunopathology is poorly understood at the molecular level and effective, precisely targeted topical therapeutics are lacking. Clinical and histological observations, as well as experimental studies, suggest involvement of the complement system in periodontitis. However, the precise roles of the various complement pathways in periodontitis have not been defined. Consequently, it is currently uncertain which specific pathways or components need to be blocked to attenuate inflammatory pathology or, alternatively, maintained intact to support host defense. At a first stage, such mechanistic and interventional approaches necessitate the use of appropriate preclinical animal models. The overall objective of this proposal is to bridge the current mechanistic deficit of complement involvement in periodontitis to allow targeted intervention. The proposed project involves a consortium arrangement between the University of Louisville School of Dentistry and the University of Pennsylvania School of Medicine, and brings together leading, complementary, and integrated expertise in the areas of periodontal inflammation, microbial immune evasion, and complement-targeted therapeutics. In Aim 1, a systematic approach is proposed to dissect the precise roles in periodontitis of individual pathways converging to or emanating from central complement hubs (C3, C5) that have already been implicated in preliminary studies. In Aim 2, it is further proposed to investigate whether novel complement-dependent microbial evasion mechanisms, first identified by this group, promote both unwarranted inflammation and the cooperative survival of periodontal bacteria. In Aim 3, those pathways or components that mediate destructive inflammation and/or pathogen persistence will be blocked, whereas those mediating host-protective effects will be kept intact. The experimental approach involves preclinical mouse models of inflammatory periodontitis and host-pathogen interactions. The mice to be used possess either intact complement system or carry specific mutations in key components that define major inductive or effector complement pathways. The translational approach involves the use of a panel of complement-specific therapeutic inhibitors. The availability of complement-specific drugs that have already undergone successful safety trials, indicates that promising interventions identified in this project have potential for rapid translation to clinical trials for periodontal disease treatment. PUBLIC HEALTH RELEVANCE: Novel Mechanisms and 'Complement-ary' Therapy in Periodontitis Project Narrative Conventional periodontal treatment is often not sufficient by itself to control destructive inflammation, which is mediated, in large part, through activities of the complement system. Our objective is to dissect mechanisms of complement involvement in periodontitis and accordingly apply appropriate complement-targeted drugs for treatment.

描述（由申请人提供）：牙周炎的新机制和“补充”治疗项目概述牙周炎炎症影响大多数成年人，而估计10-15%的人发展为严重的牙周炎，这对患者产生全身性影响（例如，动脉粥样硬化和糖尿病的风险增加）。然而，在分子水平上对潜在的免疫病理学知之甚少，并且缺乏有效的、精确靶向的局部治疗方法。临床和组织学观察，以及实验研究表明，牙周炎的补体系统的参与。然而，各种补体途径在牙周炎中的确切作用尚未确定。因此，目前尚不确定需要阻断哪些特定途径或组分以减轻炎症病理，或者维持完整以支持宿主防御。在第一阶段，这种机械和介入方法需要使用适当的临床前动物模型。这项建议的总体目标是弥合目前牙周炎中补体参与的机械缺陷，以进行有针对性的干预。拟议的项目涉及路易斯维尔大学牙科学院和宾夕法尼亚大学医学院之间的联盟安排，并汇集了牙周炎症，微生物免疫逃避和补体靶向治疗领域的领先，互补和综合专业知识。在目标1中，提出了一种系统的方法来剖析在牙周炎中的确切作用的个别途径收敛到或从中央补体枢纽（C3，C5）已经牵连在初步研究。在目的2中，进一步提出研究由该小组首次鉴定的新型补体依赖性微生物逃避机制是否促进不必要的炎症和牙周细菌的合作存活。在目标3中，介导破坏性炎症和/或病原体持续存在的那些通路或组分将被阻断，而介导宿主保护作用的那些通路或组分将保持完整。实验方法包括炎症性牙周炎和宿主-病原体相互作用的临床前小鼠模型。待使用的小鼠具有完整的补体系统或在定义主要诱导或效应补体途径的关键组分中携带特异性突变。翻译方法涉及使用一组补体特异性治疗性抑制剂。已经进行了成功的安全性试验的补体特异性药物的可用性表明，该项目中确定的有希望的干预措施有可能快速转化为牙周病治疗的临床试验。 公共卫生关系：牙周炎的新机制和“补充”治疗项目叙述传统的牙周治疗往往不足以控制破坏性炎症，这是介导的，在很大程度上，通过补体系统的活动。我们的目标是剖析补体参与牙周炎的机制，并相应地应用合适的补体靶向药物进行治疗。