Study on the roles of immunosuppressive cytokines in the establishment and progression of mycobacterial infections
Study on the roles of immunosuppressive cytokines in the establishment and progression of mycobacterial infections
批准号:
07670310
负责人:
TOMIOKA Haruaki
金额:
$1.15万
依托单位国家:
日本
项目类别:
Grant-in-Aid for Scientific Research (C)
财政年份:
1995
资助国家:
日本
项目状态:
已结题
起止时间:
1995 至 1996
中文摘要
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英文摘要
This study has deatl with the roles of immunosuppressive cytokines including IL-10 and TGF-beta in the initiation and the progression of bacterial regrowth at the sites of infection due to Mycobacterium avium complex (MAC), one of the representative atypical mycobacteria, induced in mice and, moreover, the roles of immunosuppressor macrophages (Mphis) induced in the relatively early phase (weeks 2 to 3) of infection in the establishment of persistent MAC infected mice in host mice. The following results were obtained. (1) In MAC infection in which the bacterial regrowth was initiated from weeks 2 to 4 after infection, the tissue levels of TNF-alpha, IL-10, and IFN-gamma in the lungs and spleens were temporarily elevated around weeks 2 to 4, while the TGF-beta levels in the spleen remained high during weeks 4 to 8. The transient increase in the cytokine levels was blocked by rifamycin-treatment of host mice. (2) When murine peritoneal or splenic Mphis were infected with the MAC organism … More s, the increase in Mphi production of TNF-alpha, IL-6, and IL-10 was seen during the first 3-day cultivation, whereas TGF-beta production was observed in much later phase of cultivation such as during days 7 to 14. The expression of mRNA encoding these cytokines was observed during 2 to 6 h after Mphi stimulation with the MAC.(3) TNF-alpha and IFN-gamma were found to participate in the in-vivo induction of the immunosuppressive Mphis in MAC-infected mice and play an important role in the experssion of their suppressor function against T cell mitogenesis, by enhancing Mphi production of certain effector molecules including prostaglandin E,reactive nitrogen intermediates, and phospholipids. (4) The blocking experiments using anti-IL-10 and anti-TGF-beta antibodies showed that the TNF-alpha-mediated expression of an adhesion molecule ICAM-1 in MAC-infected Mphis observed during days 1 to 3 after the initiation of Mphi cultivation was down-regulated by IL-10 and TGF-beta produced by the Mphis themselves in an autocrine fashion. These findings indicate important roles of immunosuppressive cytokines in progression of MAC infection in hosts. Less
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7.Tomioka, H.: "The role of tumor necrosis facter- in combination with interferon-1 or interieukin-1 in the immunosuppresslve macrophages because of Mycobacterium avium compiex infection." Immunology. 88. 61-67 (1996)
7.Tomioka, H.:“由于鸟分枝杆菌复合感染,肿瘤坏死因子与干扰素-1 或白细胞介素-1 结合在免疫抑制巨噬细胞中的作用。”
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9.Win Win Maw: "抗酸菌感染マクロファージにおけるICAM-1発現の制御メカニズムに関する研究(第1報)" 結核. 71. 561-567 (1996)
9.Win Win Maw:“分枝杆菌感染的巨噬细胞中ICAM-1表达控制机制的研究(首次报告)”结核病。
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13.冨岡治明: "抗酸菌症と免疫" 臨床と微生物. 24. 45-52 (1997)
13. Haruaki Tomioka:“分枝杆菌疾病和免疫”《临床和微生物学》24. 45-52 (1997)。
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冨岡治明: "らいの免疫学研究の進歩:特に、らい患者にみられる免疫不応性の成立にかかわるサイトカインとの関連から." 日本らい学会雑誌. 64. 69-84 (1995)
Haruaki Tomioka:“麻风病免疫学研究的进展:特别是与麻风病患者中观察到的免疫难治性建立有关的细胞因子。”日本麻风病学会杂志 64. 69-84 (1995)。
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10.佐藤勝昌: "intereron-γあるいはtumor necrosis factor-α処理マウス腹腔マクロファージにおける抗マイコバクテリア活性発現の様相の差異について。" 結核. 71. 607-614 (1996)
10.Katsumasa Sato:“用 Intereron-γ 或肿瘤坏死因子-α 处理的小鼠腹腔巨噬细胞中抗分枝杆菌活性的表达差异。” 结核病。
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共 48 条
Development of new antituberculous drugs based on CoMFA 3D-QSAR analysis
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批准号:23659506
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项目类别:Grant-in-Aid for Challenging Exploratory Research
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资助金额:$2.33万
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财政年份:2011
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负责人:TOMIOKA Haruaki
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依托单位:
Molecular biological study on macrophage antimicrobial mechanism based on phospholipase A_2
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批准号:20591202
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项目类别:Grant-in-Aid for Scientific Research (C)
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财政年份:2008
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负责人:TOMIOKA Haruaki
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依托单位:
Study of virulence and drug-susceptabiltly of MAC strains isolated from Japanese patients with the nodular-bronchiectasis type MAC disease
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批准号:18590850
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项目类别:Grant-in-Aid for Scientific Research (C)
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资助金额:$2.53万
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财政年份:2006
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负责人:TOMIOKA Haruaki
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依托单位:
Mechanisms of phospholipase A_2-dependent killing of microorganisms on macrophages
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批准号:16590358
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项目类别:Grant-in-Aid for Scientific Research (C)
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资助金额:$2.18万
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财政年份:2004
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负责人:TOMIOKA Haruaki
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依托单位:
Roles of free fatty acid macrophage mediated killing of mycobacteria
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批准号:13670272
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项目类别:Grant-in-Aid for Scientific Research (C)
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资助金额:$2.43万
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财政年份:2001
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负责人:TOMIOKA Haruaki
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依托单位:
STUDIES ON THE MECHANISMS FOR EXPRESSION OF THE SUPPRESSOR ACTIVITY BY MYCOBACTERIUM AVIUM COMPLEX-INDUCED IMMUNOSUPPRESSIVE MACROPHAGES
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批准号:10670255
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项目类别:Grant-in-Aid for Scientific Research (C)
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资助金额:$1.02万
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财政年份:1998
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负责人:TOMIOKA Haruaki
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依托单位:
海外基金