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New locus controlling suscept. to TB: genetics & funct.

New locus controlling suscept. to TB: genetics & funct.
新的位点控制敏感度。
批准号:
6763092
负责人:
Igor Kramnik
金额:
$40.45万
依托单位国家:
美国
项目类别:
财政年份:
2001
资助国家:
美国
项目状态:
已结题
起止时间:
2001-09-30 至 2006-06-30

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中文摘要
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英文摘要
DESCRIPTION (provided by the applicant): It is projected that a total of 225 million new cases of tuberculosis will occur between 1998 and 2030. The outcome of primary infection with Mycobacterium tuberculosis (MTB) varies and, in immunocompetent hosts, imparts only a 10 percent lifetime risk of developing clinical disease. The significant variation in tuberculosis susceptibility among immunocompetent individuals remains unexplained. Differences in the outcome of tuberculosis infection in the setting of similar risk factors support a significant role of the host genetic background in predisposition to progression towards clinical disease. Therefore, identification of genetic factors associated with susceptibility to tuberculosis will have important implications for controlling the disease. We use a mouse experimental model of infection with virulent strain of MTB to characterize genes that are responsible for control of tuberculosis infection in immunocompetent hosts. We have identified and mapped to a 2 cM interval on mouse chromosome 1 a novel locus (sst1) that significantly contributes to control of growth of virulent MTB primarily in the lungs. Observations on its phenotypic expression demonstrate that genetic mechanisms controlling infection with virulent MTB are distinct from those that control an avirulent vaccine strain of M bovis BCG. Having generated a set of sst1-congenic inbred strains of mice, we propose to use them (1) to isolate the sst1-candidate genes by positional cloning; (2) to identify genetic polymorphism responsible for tuberculosis susceptibility; (3) to identify cells and functional pathways affected by the sst1 polymorphism. The proposed project will identify the nature and mechanism of action of the sst1 in mice, which in the future should permit isolation of its human homologue and the analysis of its role in tuberculosis susceptibility in humans. The understanding of genetically determined mechanisms that operate during the course of tuberculosis infection in the lung will provide new insights into the pathogenesis of tuberculosis and suggest improved strategies for treatment and prevention of the disease.
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Necrosis in pulmonary TB granulomas: dynamics, mechanisms, therapies
  • 批准号:
    9028706
  • 项目类别:
  • 资助金额:
    $70.94万
  • 财政年份:
    2016
  • 负责人:
    Igor Kramnik
  • 依托单位:
Necrosis in Pulmonary TB granulomas: dynamics, mechanisms, and therapies
  • 批准号:
    10446079
  • 项目类别:
  • 资助金额:
    $72.48万
  • 财政年份:
    2016
  • 负责人:
    Igor Kramnik
  • 依托单位:
Necrosis in Pulmonary TB granulomas: dynamics, mechanisms, and therapies
  • 批准号:
    10584526
  • 项目类别:
  • 资助金额:
    $69.51万
  • 财政年份:
    2016
  • 负责人:
    Igor Kramnik
  • 依托单位:
Novel TB Treatment Strategy - Optimization of Macrophage Responsiveness to IFNy
  • 批准号:
    9033071
  • 项目类别:
  • 资助金额:
    $49.11万
  • 财政年份:
    2013
  • 负责人:
    Igor Kramnik
  • 依托单位: