GENETIC AND IMMUNOLOGIC ASPECTS OF PERIODONTAL DISEASES

牙周疾病的遗传和免疫学方面

• 批准号: 6651157
• 负责人: HARVEY Allen SCHENKEIN
• 金额: $ 153.11万
• 依托单位: VIRGINIA COMMONWEALTH UNIVERSITY
• 依托单位国家: 美国
• 财政年份: 2000
• 资助国家: 美国
• 起止时间: 2000-07-01 至 2005-06-30
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/6651157
• 关键词: bactericidal immunity; genetic susceptibility; human subject; periodontitis; periodontium disorder

Studies of genetic and immunologic aspects of periodontal diseases. The overall goal of the proposed research is to address significant questions in periodontology via an integrated approach that exploits investigator expertise in human genetics, immunology, and bacterial pathogenesis. The investigators participating in these projects have worked together successfully for many years and were most recently supported by a Periodontal Disease Research Center grant form NIDR. We now propose a series of projects tied together as a Program Project; we propose to support a Core facility that provides administrative, clinical, and biostatistical support to the other projects. Each project will rely upon the Core for support of its scientific goals. Four interrelated and integrated scientific projects are proposed. We have been studying genetic aspects of early-onset periodontal diseases (EOP) for several years and have identified a specific gene (IL-1 on chromosome 2q) and a chromosomal region (19q) involved in EOP susceptibility. Additional chromosomal regions are strongly suggested, providing a rationale for continuing and expanding these studies. Secondly, we have been studying antibody responses and immunoglobulin production in periodontitis patients; major findings have been the observations that serum IgG2 levels are a heritable trait, and that IgG2 serum concentrations are significantly higher in some EOP patients than in healthy individuals or AP patients. These observations form the foundation for 3 higher in some EOP patients than in healthy individuals or AP patients. These observations form the foundation for 3 additional projects. The contribution of cytokines, including Il-1 (which is involved in EOP susceptibility, and levels of which are genetically determined), and lipid mediators (including PGE2 and PAF) to IgG2 production will be examined. Further, the contribution of PAG regulatory enzyme PAG acetyl-hydrolase, which is produced in low concentrations by monocytes from LJP patients, will be studied, Additionally, we have discovered that IgG2 antibody levels against phosphorylcholine (PC) are elevated in patients with periodontal attachment loss compared to healthy subjects; this led us to the observations that anti-PC inhibits IgG2 production and that several plaque microorganisms associated with periodontal destruction (A. actinomycetemcomitans, F. nucleatum) and endocaritis (S. sanguis), may have PC. The significance of this a-PC antibody and oral bacterial PC will be examined, and genetic control of a-PC levels will be explored.

牙周病的遗传学和免疫学研究。拟议研究的总体目标是通过利用研究人员在人类遗传学，免疫学和细菌发病机制方面的专业知识的综合方法来解决牙周病学中的重大问题。参与这些项目的研究人员已经成功地合作了多年，最近得到了NIDR牙周病研究中心的资助。我们现在提出了一系列项目捆绑在一起作为一个计划项目;我们建议支持一个核心设施，提供行政，临床和生物统计支持的其他项目。每个项目都将依靠核心来支持其科学目标。提出了四个相互关联和综合的科学项目。我们已经研究早发性牙周病（EOP）的遗传方面几年，并确定了一个特定的基因（IL-1的染色体2 q）和染色体区域（19 q）参与EOP的易感性。强烈建议增加染色体区域，为继续和扩大这些研究提供了依据。其次，我们一直在研究牙周炎患者的抗体反应和免疫球蛋白的产生;主要发现是观察到血清IgG 2水平是一种遗传性状，并且某些EOP患者的IgG 2血清浓度显著高于健康个体或AP患者。这些观察结果形成了某些EOP患者比健康个体或AP患者高3的基础。这些观察结果构成了另外3个项目的基础。将检查细胞因子，包括IL-1（参与EOP易感性，其水平由遗传决定）和脂质介质（包括PGE 2和PAF）对IgG 2产生的贡献。此外，将研究PAG调节酶PAG乙酰水解酶的贡献，所述PAG乙酰水解酶由来自LJP患者的单核细胞以低浓度产生。此外，我们已经发现，与健康受试者相比，牙周附着丧失患者中抗磷酸胆碱（PC）的IgG 2抗体水平升高;这使我们观察到抗PC抑制IgG 2的产生，并且几种与牙周破坏有关的菌斑微生物（A. actinomycetemcomitans、F. nucleatum）和软骨内膜炎（S.可能有PC。将检查这种a-PC抗体和口腔细菌PC的意义，并探索a-PC水平的遗传控制。