A basic studies to develop the immune therapy for periodontal diseases by employing glycolipids derived from periodontal bacteria as antigens.
A basic studies to develop the immune therapy for periodontal diseases by employing glycolipids derived from periodontal bacteria as antigens.
批准号:
15592199
负责人:
OHYAMA Hideki
金额:
$2.18万
依托单位国家:
日本
项目类别:
Grant-in-Aid for Scientific Research (C)
财政年份:
2003
资助国家:
日本
项目状态:
已结题
起止时间:
2003 至 2004
中文摘要
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英文摘要
This study is the first trial to establish the immune therapy for periodontal diseases by using glycolipid antigens derived from periodontal bacteria. It has been reported that the existence of T cells recognize the glycolipid antigens in context of CD1 molecules expressed on dendritic cells(DCs). These phenomena led us to have a hypothesis that the immune responses against glycolipids from periodontal bacteria were involved in the host defense of periodontal patients. To clarify the possibility of this issue, we tried to identify the glycolipid antigens derived from periodontal bacteria, CD1 molecules and T cell populations. We succeeded in obtaining the glycolipids showing high polarity derived from sonic extracts of three bacteria, including A.actinomycetemcomitans, P.gingivalis and T denticola. These glycolipids were mixed and added in the culture of DCs to be presented efficiently by CD1 molecules expressed on DCs. We co-cultured T cells from healthy volunteers with these DCs derived from irrelevant donors for several weeks. As a result, we succeeded in establishing 16 T cell lines from 3 healthy donors, which showed specific response against glycolipid antigens derived from these bacteria. To identify the glycolipid antigens inducing T cell proliferative responses, we separated the extract materials into several fractions and evaluated T cell proliferative responses in the presence of each fraction as antigen. As a result, it was revealed that there were several fractions inducing T cell responses, and that most of T cells induced by these fractions were CD4 positive. These findings elucidated that several glycolipids derived from periodontal bacteria would be possible antigens to induce the proliferative responses of CD4 positive T cells.
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Yoshihiko Soga: "Tumor necrosis factor-alpha gene(TNF-α)-1031/-863,-857 single nucleotide polymorphisms(SNPs)are associated with severe adult periodontitis in Japanese."Journal of Clinical Periodontology. 30・6. 524-531 (2003)
Yoshihiko Soga:“肿瘤坏死因子-α基因(TNF-α)-1031/-863、-857单核苷酸多态性(SNP)与日本成人严重牙周炎有关。”临床牙周病学杂志30・6。 531(2003)
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DOI:
10.1034/j.1600-051x.2003.00287.x
发表时间:
2003-06-01
期刊:
JOURNAL OF CLINICAL PERIODONTOLOGY
影响因子:
6.7
作者:
[Soga, Y, Nishimura, F, Murayama, Y]
通讯作者:
Murayama, Y
Hideki Ohyama: "SNPs on IL-12 receptor gene associated with the susceptibility to leprosy."US-Japan Cooperative Medical Science Program. 38. 105-110 (2003)
Hideki Ohyama:“IL-12 受体基因上的 SNP 与麻风病易感性相关。”美日合作医学科学计划。
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松島 綱治: "分子予防環境医学 -生命科学研究の予防・環境医学への統合-"分子予防環境医学研究会. 768 (2003)
Tsunaharu Matsushima:“分子预防环境医学-生命科学研究与预防和环境医学的整合”分子预防环境医学研究组768(2003)。
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Positional effect of amino acid replacement on peptide antigens for the increased IFN-γ production from CD4 T cells.
氨基酸替换对肽抗原的位置影响,以增加 CD4 T 细胞的 IFN-γ 产量。
DOI:
--
发表时间:
2005
期刊:
Allergology International 54(1)
影响因子:
--
作者:
[Liu, T., Kohsaka, H., Suzuki, M., Takagi, R., Hashimoto, K., Uemura, Y., Ohyama, H., Matsushita, S.]
通讯作者:
S.
共 17 条
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批准号:20592443
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项目类别:Grant-in-Aid for Scientific Research (C)
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资助金额:$2.91万
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财政年份:2008
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负责人:OHYAMA Hideki
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依托单位:
A study for the involvement of IL-22 in the pathogenesis of periodontal diseases
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批准号:18592274
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项目类别:Grant-in-Aid for Scientific Research (C)
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资助金额:$2.57万
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财政年份:2006
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负责人:OHYAMA Hideki
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依托单位:
海外基金