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DESCRIPTION (provided by applicant): New case detection rates in leprosy remain obstinately high despite years of global coverage with multiple drug therapy (MDT) and a major decrease in prevalence. This fact demonstrates clearly that treatment alone does not block transmission of leprosy and underscores major gaps in our comprehension of the disease; we do not know how leprosy is transmitted and we have not fully developed or assessed promising tools for detecting preclinical leprosy, a possible source of transmission, or tracing individual isolates within communities. Under previous support, this consortium identified Mycobacterium leprae specific proteins and peptides, promising in cell mediated immune assays in leprosy endemic regions, and sufficient genetic diversity within M. leprae genomes to trace individual isolates, globally and locally. The continuing development of these tools in leprosy endemic regions of Brazil, and subsequently through the newly formed IDEAL (Initiative for Diagnostic and Epidemiological Assays for Leprosy) global network, to address transmission and early diagnosis, are the major foci of the proposed research. Also, as biomarkers for disease susceptibility, notably nerve damage and disability, both protective and disease inducing cytokines will be determined with the aim of identifying antigens able to induce a discriminating T cell phenotype in leprosy patients compared to controls. This program, the culmination of a career in basic research, will bring to leprosy control programs the means to assess the effects of chemotherapeutic intervention on disease incidence, and point the way to eradication of a disease that afflicts the most impoverished of humanity.
期刊论文(31)
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Postgenomic Mycobacterium leprae antigens for cellular and serological diagnosis of M. leprae exposure, infection and leprosy disease.
用于麻风分枝杆菌暴露、感染和麻风病的细胞和血清学诊断的基因组后麻风分枝杆菌抗原。
DOI: --
发表时间: 2011
期刊: Leprosy review
影响因子: 0.6
作者: [Geluk,Annemieke, Duthie,MalcolmS, Spencer,JohnS]
通讯作者: Spencer,JohnS
DOI: 10.1128/jcm.00239-08
发表时间: 2008-05
期刊: Journal of Clinical Microbiology
影响因子: 9.4
作者: [M. Monot;N. Honoré;C. Balière;B. Ji;S. Sow;P. Brennan;S. Cole]
通讯作者: M. Monot;N. Honoré;C. Balière;B. Ji;S. Sow;P. Brennan;S. Cole
IDEAL: in the footsteps of IMMLEP and THELEP.
理想:追随 IMMLEP 和 THELEP 的脚步。
DOI: --
发表时间: 2009
期刊: Leprosy review
影响因子: 0.6
作者: [Brennan,PatrickJ]
通讯作者: Brennan,PatrickJ
Molecular drug susceptibility testing and genotyping of Mycobacterium leprae strains from South America.
南美洲麻风分枝杆菌菌株的分子药物敏感性测试和基因分型。
DOI: 10.1128/aac.00201-11
发表时间: 2011
期刊: Antimicrobial agents and chemotherapy
影响因子: 4.9
作者: [Singh,Pushpendra, Busso,Philippe, Paniz-Mondolfi,Alberto, Aranzazu,Nacarid, Monot,Marc, Honore,Nadine, deFariaFernandesBelone,Andrea, Virmond,Marcos, Villarreal-Olaya,MariaEsther, Rivas,Carlos, Cole,StewartT]
通讯作者: Cole,StewartT
13
    Lipid Antigens for iNKT Cells in the Gut Microenvironment
    • 批准号:
      10339377
    • 项目类别:
    • 资助金额:
      $40.33万
    • 财政年份:
      2020
    • 负责人:
      Patrick Joseph Brennan
    • 依托单位:
    Lipid Antigens for iNKT Cells in the Gut Microenvironment
    • 批准号:
      10555286
    • 项目类别:
    • 资助金额:
      $40.33万
    • 财政年份:
      2020
    • 负责人:
      Patrick Joseph Brennan
    • 依托单位:
    Self and dietary lipid antigens for invariant natural killer T cells
    • 批准号:
      8842452
    • 项目类别:
    • 资助金额:
      $18.4万
    • 财政年份:
      2013
    • 负责人:
      Patrick Joseph Brennan
    • 依托单位:
    Self and dietary lipid antigens for invariant natural killer T cells
    • 批准号:
      8580641
    • 项目类别:
    • 资助金额:
      $18.4万
    • 财政年份:
      2013
    • 负责人:
      Patrick Joseph Brennan
    • 依托单位:
    海外基金