Induction of inflammatory immune response by streptococcal water-insoluble α-glucans and association with periodontal diseases
Induction of inflammatory immune response by streptococcal water-insoluble α-glucans and association with periodontal diseases
批准号:
16591824
负责人:
OKAMOTO Shigefumi
金额:
$2.3万
依托单位:
依托单位国家:
日本
项目类别:
Grant-in-Aid for Scientific Research (C)
财政年份:
2004
资助国家:
日本
项目状态:
已结题
起止时间:
2004 至 2005
中文摘要
不溶于水的α-葡聚糖(WIG)是由变形链球菌的糖基转移酶i合成的,在牙菌斑的形成中起重要作用。我们发现由sobrinus链球菌合成的WIG激活小鼠腹膜渗出巨噬细胞产生细胞因子。免疫反应不是由蔗糖、水溶性葡聚糖、脂多糖或肽聚糖污染引起的。WIG刺激人单核细胞产生TNF-α和IL-8。人多形核细胞也被WIG激活,导致细胞趋化和过氧化氢的产生。这些结果表明,WIG调节巨噬细胞和粒细胞诱导的炎症免疫反应。此外,由于WIG直接损伤人口腔鳞状细胞,我们推测α-葡聚糖诱导的口腔鳞状细胞损伤和炎症与牙周病的发生有关。
英文摘要
Water-insoluble α-glucans (WIG) are synthesized from sucrose by the glucosyltransferase-I of mutans streptococci, that play an important role in the development of dental plaque. We found that WIG synthesized by Streptococcus sobrinus activated mouse peritoneal exudate macrophages to produce cytokines. The immunological responses were not due to contamination by sucrose, water-soluble glucan, lipopolysaccharide, or peptidoglycan. WIG stimulated human monocytes to produce TNF-α and IL-8. Human polymorphonuclear cells were also activated by WIG, resulting in chemotaxis of the cells and production of hydrogen peroxide. These results suggest that WIG modulate macrophage- and granulocyte-induced inflammatory immune responses. Furthermore, since WIG injured human oral squamous cells directly, we speculate that oral squamous cell injury and inflammation induced by α-glucans are associated with the development of periodontal diseases.
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Systemic immunization with streptococcal immunoglobulin-binding protein Sib35 induces protective immune responses against group A Streptococcus challenge in mice
使用链球菌免疫球蛋白结合蛋白 Sib35 进行全身免疫可诱导小鼠针对 A 族链球菌攻击的保护性免疫反应
DOI:
--
发表时间:
2005
期刊:
Vaccine (印刷中)
影响因子:
--
作者:
[Okamoto, S., et al.]
通讯作者:
et al.
Protective immunity against Streptococcus pyogenes challenge in mice following immunization with fibronectin-binding protein
纤连蛋白结合蛋白免疫小鼠后对化脓性链球菌攻击的保护性免疫
DOI:
--
发表时间:
2005
期刊:
Journal of Infectious Diseases 192
影响因子:
--
作者:
[Terao Y, Okamoto S, Kataoka K, Hamada S, Kawabata S]
通讯作者:
Kawabata S
DOI:
10.1016/j.vaccine.2005.02.035
发表时间:
2005-09-23
期刊:
VACCINE
影响因子:
5.5
作者:
[Okamoto, S, Tamura, Y, Kawabata, S]
通讯作者:
Kawabata, S
International Congress Series Vol : 1263
国际大会系列卷:1263
DOI:
--
发表时间:
2004
期刊:
影响因子:
--
作者:
[Ryoji Fujimaki, Katsuhiko Hayashi, Naoko Watanabe, Taketo Yamada, Yoshiaki Toyama, Ken-ichi Tezuka, Nobumichi Hozumi, Bae YC, Kawano S, Kawaoka Y]
通讯作者:
Kawaoka Y
A model of invasive type of Streptococcus pyogenes infection after intranasal infection in influenza A virus.
甲型流感病毒鼻内感染后侵袭型化脓性链球菌感染模型。
DOI:
--
发表时间:
2004
期刊:
International Congress Series 163
影响因子:
--
作者:
[Okamoto, S., Kawabata, S., Nakagawa, I., Okuno, Y., Goto, T., Sano, K., Hamada, S.]
通讯作者:
S.
共 7 条
Mechanism of invasive diseases by superinfection with influenza virus and oral Streptococcus
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批准号:26462806
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项目类别:Grant-in-Aid for Scientific Research (C)
-
资助金额:$3.08万
-
财政年份:2014
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负责人:OKAMOTO Shigefumi
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依托单位: