Study on the roles of immunosuppressive cytokines in the establishment and progression of mycobacterial infections

免疫抑制细胞因子在分枝杆菌感染发生和进展中的作用研究

基本信息

  • 批准号:
    07670310
  • 负责人:
  • 金额:
    $ 1.15万
  • 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:
    1995
  • 资助国家:
    日本
  • 起止时间:
    1995 至 1996
  • 项目状态:
    已结题

项目摘要

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
本研究探讨了IL-10和TGF-β等免疫抑制细胞因子在小鼠非典型分枝杆菌复合体(MAC)感染部位细菌再生长的启动和进展中的作用,免疫抑制巨噬细胞(Mphis)诱导的相对早期阶段(2至3周)在建立持续MAC感染小鼠在宿主小鼠中的作用。获得了以下结果。(1)在MAC感染中,其中细菌再生长在感染后第2至4周开始,肺和脾中TNF-α、IL-10和IFN-γ的组织水平在第2至4周左右暂时升高,而脾中的TGF-β水平在第4至8周期间保持高水平。细胞因子水平的瞬时增加被宿主小鼠的利福霉素治疗阻断。(2)当小鼠腹膜或脾Mphis感染MAC生物体时, ...更多信息 s,在前3天培养期间观察到TNF-α、IL-6和IL-10的Mphi产生的增加,而在培养的更晚阶段例如在第7至14天期间观察到TGF-β产生。在用MAC刺激Mphi后2至6 h期间观察编码这些细胞因子的mRNA的表达。(3)发现TNF-α和IFN-γ参与MAC感染小鼠中免疫抑制性Mphis的体内诱导,并通过增强某些效应分子(包括前列腺素E、活性氮中间体和磷脂)的Mphi产生,在其针对T细胞有丝分裂的抑制功能的表达中发挥重要作用。(4)使用抗IL-10和抗TGF-β抗体的阻断实验表明,在开始Mphi培养后的第1至3天期间观察到的MAC感染的Mphis中TNF-α介导的粘附分子ICAM-1的表达被Mphis自身以自分泌方式产生的IL-10和TGF-β下调。这些发现表明免疫抑制细胞因子在宿主MAC感染的进展中起重要作用。少

项目成果

期刊论文数量(48)
专著数量(0)
科研奖励数量(0)
会议论文数量(0)
专利数量(0)
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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    0
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  • 通讯作者:
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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    0
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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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    0
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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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    0
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Haruaki Tomioka: "The reason Why mycobacterial infections are intractable : Recent studies on animal experimental models of Mycobacterium avium complex infections. (in Japanese)" Jap.J.Lepr.65. 155-165 (1996)
Haruaki Tomioka:“分枝杆菌感染难以治愈的原因:鸟分枝杆菌复合感染动物实验模型的最新研究。(日语)”Jap.J.Lepr.65。
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    0
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TOMIOKA Haruaki其他文献

TOMIOKA Haruaki的其他文献

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{{ truncateString('TOMIOKA Haruaki', 18)}}的其他基金

Development of new antituberculous drugs based on CoMFA 3D-QSAR analysis
基于CoMFA 3D-QSAR分析的抗结核新药开发
  • 批准号:
    23659506
  • 财政年份:
    2011
  • 资助金额:
    $ 1.15万
  • 项目类别:
    Grant-in-Aid for Challenging Exploratory Research
Molecular biological study on macrophage antimicrobial mechanism based on phospholipase A_2
基于磷脂酶A_2的巨噬细胞抗菌机制的分子生物学研究
  • 批准号:
    20591202
  • 财政年份:
    2008
  • 资助金额:
    $ 1.15万
  • 项目类别:
    Grant-in-Aid for Scientific Research (C)
Study of virulence and drug-susceptabiltly of MAC strains isolated from Japanese patients with the nodular-bronchiectasis type MAC disease
日本结节性支气管扩张型 MAC 病患者 MAC 菌株毒力及药敏研究
  • 批准号:
    18590850
  • 财政年份:
    2006
  • 资助金额:
    $ 1.15万
  • 项目类别:
    Grant-in-Aid for Scientific Research (C)
Mechanisms of phospholipase A_2-dependent killing of microorganisms on macrophages
磷脂酶A_2依赖性巨噬细胞杀灭微生物的机制
  • 批准号:
    16590358
  • 财政年份:
    2004
  • 资助金额:
    $ 1.15万
  • 项目类别:
    Grant-in-Aid for Scientific Research (C)
Roles of free fatty acid macrophage mediated killing of mycobacteria
游离脂肪酸巨噬细胞介导的分枝杆菌杀伤作用
  • 批准号:
    13670272
  • 财政年份:
    2001
  • 资助金额:
    $ 1.15万
  • 项目类别:
    Grant-in-Aid for Scientific Research (C)
STUDIES ON THE MECHANISMS FOR EXPRESSION OF THE SUPPRESSOR ACTIVITY BY MYCOBACTERIUM AVIUM COMPLEX-INDUCED IMMUNOSUPPRESSIVE MACROPHAGES
鸟分枝杆菌复合体诱导的免疫抑制巨噬细胞表达抑制活性的机制研究
  • 批准号:
    10670255
  • 财政年份:
    1998
  • 资助金额:
    $ 1.15万
  • 项目类别:
    Grant-in-Aid for Scientific Research (C)

相似海外基金

identification of M.avium complex and exacerbation factor of pulmonary MAC disease by mass spectrometry
质谱法鉴定鸟分枝杆菌复合体及肺MAC疾病恶化因子
  • 批准号:
    15K19416
  • 财政年份:
    2015
  • 资助金额:
    $ 1.15万
  • 项目类别:
    Grant-in-Aid for Young Scientists (B)
Multiplex TB-M.avium complex Fluorescent in Situ hybridization Assay, direct from
多重 TB-M.avium 复合物荧光原位杂交检测,直接来自
  • 批准号:
    7749251
  • 财政年份:
    2009
  • 资助金额:
    $ 1.15万
  • 项目类别:
食細胞機能抑制マウスにおけるM.avium complex感染症の解析及び治療
吞噬功能抑制小鼠鸟分枝杆菌复合体感染的分析及治疗
  • 批准号:
    05670524
  • 财政年份:
    1993
  • 资助金额:
    $ 1.15万
  • 项目类别:
    Grant-in-Aid for General Scientific Research (C)
CD4欠損マウスにおけるM.avium complex(MAC)感染動態と解析と治療の開発
CD4 缺陷小鼠中鸟分枝杆菌复合体 (MAC) 感染动态和治疗的分析和发展
  • 批准号:
    04670465
  • 财政年份:
    1992
  • 资助金额:
    $ 1.15万
  • 项目类别:
    Grant-in-Aid for General Scientific Research (C)
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