Prevention and treatment of periodntal disease ; the developments of mucosal vaccination and protease inhibitor

牙周病的预防和治疗;

基本信息

  • 批准号:
    11557133
  • 负责人:
  • 金额:
    $ 8.64万
  • 依托单位:
  • 依托单位国家:
    日本
  • 项目类别:
    Grant-in-Aid for Scientific Research (B)
  • 财政年份:
    1999
  • 资助国家:
    日本
  • 起止时间:
    1999 至 2001
  • 项目状态:
    已结题

项目摘要

This study deals with local and systemic immune responses to Porphyromonas gingivalis ATCC 33277 fimbriae after mucosal vaccination of mice via intranasal route with the fimbriae and recombinant cholera toxin B subunit (rCTB). The fimbriae by itself stimulated systemic immune responses even at a low dose (0.5 μg), and serum IgG and IgA specific to P. gingivalis fimbriae were induced in an antigen dose-dependent manner. Induction of the serum IgG and IgA was started from 10 days after the first immunization, and the levels continued to elevate until sacrifice day. rCTB co-administration did not enhance the levels of systemic responses, but the levels of serum IgA were slightly increased by rCTB-adjuvant effect when the mice was immunized with 0.5 μg of the fimbriae. The serum IgG subclass titers were revealed to be the order of IgG1 > IgG3 > IgG2b > IgG2a, suggesting that Th1 and Th2 type immune systems were stimulated by this immunization. In addition to systemic response, mucosal vacc … More ination with P. gingivalis fimbriae more than 5 μg also stimulated mucosal IgA response which was started to elevated from 18 days after the first immunization. The mucosal IgA response was significantly enhanced by rCTB co-administration, and in particular, secretory IgA specific to P. gingivalis fimbriae was induced into saliva, nosal cavity and lung at a high level even at a low dose (0.5 μg fimbriae). Thus, the mucosal vaccination with co-administration of P. ginigvalis fimbriae and rCTB via intranasal route strongly stimulated not only systemic immune response but also mucosal response, indicating that this vaccination may be efficacious for the prevention of P. gingivalis-mediated periodontal disease.In addition, an approximately 80 % reduction of P. gingivalis-mediated alveolar bone resorption in mice was induced by nasal administration of the fimbrial vaccine.Thus, nasal administration of the vaccine containing fimbriae and rCTB strongly stimulated both systemic and mucosal responses and may be effective for the prevention of P. gingivalis-mediated periodontitis. Less
这项研究涉及局部和全身免疫反应对小鼠粘膜疫苗在小鼠粘膜疫苗通过鼻内途径的粘膜和重组霍乱毒素B亚基(RCTB)的粘膜疫苗(RCTB)。即使在低剂量(0.5μg)下,叶片本身也刺激了全身免疫反应,并且以抗原剂量依赖性方式诱导了对牙龈斑ap虫纤维化膜的血清IgG和IgA。血清IgG和IgA的诱导是从第一次免疫抑制后的10天开始的,水平继续升高到牺牲日。 RCTB共同给药并不能提高全身反应的水平,但是当小鼠用0.5μg的纤维膜免疫时,RCTB-Adjuvant效应略微增加了血清IgA的水平。血清IgG亚类滴度显示为IgG1> IgG3> IgG2B> IgG2A的顺序,这表明TH1和TH2型免疫系统受到这种免疫配置的刺激。除了系统性反应外,粘膜Vac…与牙龈疟原虫纤维化膜的更多相互关系超过5μg,还刺激了粘膜IGA反应,从第一次免疫配置后的18天开始,该反应开始升高。 RCTB共同给药显着增强了粘膜IgA反应,尤其是,即使在低剂量下(0.5μgfimbriae),也可以将特定于牙龈牙龈牙龈利疟原虫的秘密IgA诱导到唾液,nosal腔和肺中。这是,通过鼻内途径与ginigvalis fimbriae和rctb共同给药的粘膜疫苗不仅强烈刺激不仅是全身免疫反应,而且还强烈刺激了粘膜反应,而且粘膜反应也可以有效,表明该疫苗可以有效地预防牙龈杂志介导的周期性疾病。通过鼻施用纤维疫苗。因此,含有fimbriae和RCTB的疫苗的鼻施用强烈刺激了全身和粘膜反应,并且可能有效预防牙龈疟原虫介导的牙周炎。

项目成果

期刊论文数量(30)
专著数量(0)
科研奖励数量(0)
会议论文数量(0)
专利数量(0)
Hamada, N.: "Cytokine production induced by a 67-kDa fimbrial protein from Porphyromonas gingivalis"Oral Microbiol. Immun.. 17. 197-200 (2002)
Hamada, N.:“由牙龈卟啉单胞菌的 67 kDa 菌毛蛋白诱导的细胞因子产生”口腔微生物。
  • DOI:
  • 发表时间:
  • 期刊:
  • 影响因子:
    0
  • 作者:
  • 通讯作者:
Sojar, H.T.: "Role of the amino-terminal region of Porphyrornonas gingivalis firnbriae in adherence to epithelial cells"Infect. Immun.. 67. 6173-6176 (1999)
Sojar, H.T.:“牙龈卟啉单胞菌的氨基末端区域在粘附上皮细胞中的作用”感染。
  • DOI:
  • 发表时间:
  • 期刊:
  • 影响因子:
    0
  • 作者:
  • 通讯作者:
Arai, M.: "Purification and characterization of a novel secondary fimbrial protein from Porphyrornonas gingivalis strain 381"FEMS Microbiol. Let.. 193. 75-81 (2000)
Arai, M.:“牙龈卟啉单胞菌菌株 381 中新型次级菌毛蛋白的纯化和表征”FEMS Microbiol。
  • DOI:
  • 发表时间:
  • 期刊:
  • 影响因子:
    0
  • 作者:
  • 通讯作者:
Arai, M.: "Purification and characterization of a novel secondary fimbrial protein from Porphyromonas gingivalis strain 381"FMS Mirobiol. Let.. 193. 75-81 (2000)
Arai, M.:“来自牙龈卟啉单胞菌菌株 381 的新型次级菌毛蛋白的纯化和表征”FMS Mirobiol。
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    0
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UMEMOTO Toshio其他文献

UMEMOTO Toshio的其他文献

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{{ truncateString('UMEMOTO Toshio', 18)}}的其他基金

Establishment of Transformation System on Periodontopathic Bacteria and Analysis of Pathogenic Factors
牙周病菌转化体系的建立及致病因素分析
  • 批准号:
    11470383
  • 财政年份:
    1999
  • 资助金额:
    $ 8.64万
  • 项目类别:
    Grant-in-Aid for Scientific Research (B)
Molecular biological analysis of virulent factors on P. gingivalis related with periodontal disease
牙龈卟啉单胞菌与牙周病相关毒力因子的分子生物学分析
  • 批准号:
    08457485
  • 财政年份:
    1996
  • 资助金额:
    $ 8.64万
  • 项目类别:
    Grant-in-Aid for Scientific Research (B)
Comstruction of a physical and gene map of periodontpathic bacterial genome
牙周病细菌基因组物理和基因图谱的构建
  • 批准号:
    05454493
  • 财政年份:
    1993
  • 资助金额:
    $ 8.64万
  • 项目类别:
    Grant-in-Aid for General Scientific Research (B)
Studies on Immunobiological Properties of Periodontopathic Bacteria
牙周病细菌的免疫生物学特性研究
  • 批准号:
    60570860
  • 财政年份:
    1985
  • 资助金额:
    $ 8.64万
  • 项目类别:
    Grant-in-Aid for General Scientific Research (C)

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    31070819
  • 批准年份:
    2010
  • 资助金额:
    33.0 万元
  • 项目类别:
    面上项目

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Mechanisms of Immune Dysfunction in Oral Post-Acute Sequelae of Covid-19
Covid-19口腔急性后遗症中免疫功能障碍的机制
  • 批准号:
    10892624
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  • 批准号:
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  • 批准号:
    8015158
  • 财政年份:
    2006
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    $ 8.64万
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Oral immunity and adjuvant receptors
口腔免疫和佐剂受体
  • 批准号:
    8693614
  • 财政年份:
    2006
  • 资助金额:
    $ 8.64万
  • 项目类别:
Oral immunity and adjuvant receptors
口腔免疫和佐剂受体
  • 批准号:
    8288025
  • 财政年份:
    2006
  • 资助金额:
    $ 8.64万
  • 项目类别:
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