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The immunologically and molecular biologically investigation for diagnostic methods of periodontal disease activity

The immunologically and molecular biologically investigation for diagnostic methods of periodontal disease activity
牙周病活动性诊断方法的免疫学和分子生物学研究
批准号:
06304041
负责人:
OKADA Hiroshi
金额:
$10.5万
依托单位:
依托单位国家:
日本
项目类别:
Grant-in-Aid for Co-operative Research (A)
财政年份:
1994
资助国家:
日本
项目状态:
已结题
起止时间:
1994 至 1995

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中文摘要
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英文摘要
This study was designed to immunologically and molecular biologically evaluate the diseased conditions of periodontitis and develop procedures to diagnose active lesions and susceptible patients. The techniques utilizing DNA probes and polymerase chain reaction were introduced to sensitively detect and identify periodontopathic bacteria in subgingival plaque. It was shown that P.gingivalis (Pg) was frequently detected in active diseased lesions. Additionally, T.denticola (Td) was always found in the unsuccessfully treated periodontal lesions but not in the successfully treated lesions, suggesting that Td would be a diagnostic indicator of the diseased conditions in the lesions after periodontal treatments. It was also suggested that Vgamma9/Vdelta2 T cells may play an important role in prevention of bacterial infection or tissue destruction. Futhermore, immune response against heat shock protein (HSP) 60 may react with both periodontitis-associated microorganisms and host cells because … More HSP 60 specific antibodies of periodontitis patients crossreact to proteins isolated from gingival fibroblast. In addition, it was also indicated that the levels of serum actibodies specific to Pg could be used as a risk indicator for the progression of periodontal diseases, because the susceptible patients to periodontal diseases exhibited significantly higher anti-Pg antibody levels than the resistant patients. Furthermore, the high levels of polyamines, alkaline phosphatase, platelet-activating factor activities, neutrophil lysosomal proteinase (medullasin and cathepsin G), secretory leukocyte protease inhibitor (SLPI), inflammatory cytokines (IL-1, IL-6, Il-8) and prostaglandin E_2 were frequently observed in gingival crevicular fluid. Also pH in periodontal pockets was significantly high in the sites with deep probing depth. Parameters showing above seem to be useful to diagnose active periodontal diseases. In conclusion, it was suggested that the combining host immune responses, inflammatory cytokines and mediators in local diseased sites examined in this study may enable us to diagnose periodontal dosease activity. Less
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会议论文
K. Kunimatsu, et al.: "Identification and possible function of cathepsin G in gingival crevicular fluid from chronic adult periodontitis patients and from experimental gingivitis subjects" Journal of Periodontal Research. 30. 51-57 (1995)
K. Kunimatsu 等人:“慢性成人牙周炎患者和实验性牙龈炎受试者龈沟液中组织蛋白酶 G 的鉴定及其可能功能”《牙周研究杂志》。
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作者: []
通讯作者:
村井 正大 ら: "唾液、GCF中のALP活性について" 日本歯学. 70(掲載予定). (1996)
Masahiro Murai 等人:“关于唾液和 GCF 中的 ALP 活性”,Nippon Dentistry 70(待出版)。
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通讯作者:
O.Fujise et al: "Colorimetric microtiter plate based assay for detection and quantification of amplified Actinobacillus actinocycetemcomitans DNA" Oral Microbiology and Immunology. 10. 372-377 (1995)
O.Fujise 等人:“基于比色微量滴定板的检测和定量扩增的放线杆菌伴放线菌 DNA”口腔微生物学和免疫学。
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作者: []
通讯作者:
K.Kunimatsu et al: "Identification and possible function of cathepsin G in gingival crevicular fluid from chronic adult periodontitis patients and from experimental gingivitis subjects" Journal of Periodontal Reseach. 30. 51-57 (1995)
K.Kunimatsu 等人:“慢性成人牙周炎患者和实验性牙龈炎受试者龈沟液中组织蛋白酶 G 的鉴定和可能功能”《牙周研究杂志》。
DOI: --
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作者: []
通讯作者:
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