Antibacterial Resistance Leadership Group (ARLG)

抗菌素耐药性领导小组 (ARLG)

基本信息

  • 批准号:
    10308017
  • 负责人:
  • 金额:
    $ 1472.99万
  • 依托单位:
  • 依托单位国家:
    美国
  • 项目类别:
  • 财政年份:
    2013
  • 资助国家:
    美国
  • 起止时间:
    2013-06-01 至 2026-11-30
  • 项目状态:
    未结题

项目摘要

Our goal is to continue to advance the successful, multidisciplinary research agenda of the Antibacterial Resistance Leadership Group (ARLG). In the original award period, the ARLG agenda increased scientific knowledge of antibacterial resistance and sought to mitigate important factors that drive its expansion. We continue to pair an unprecedented team of over two dozen of the world's top investigators with the organizational excellence of the Duke Clinical Research Institute (DCRI), one of the world's largest Academic Research Organizations. Because of the complexity of integrating multiple components of such a large-scale clinical research network, our renewal continues to feature centralized leadership through an Executive Committee and a dual PI approach. One PI (Fowler) focuses primarily on operations and the other (Chambers) focuses largely on scientific agenda. The organizational structure also features Scientific Subcommittees devoted to three priority areas: Gram-negative bacterial infections, Gram-positive bacterial infections, and Diagnostics. These Subcommittees are supported by internationally recognized Collaborating Investigators to advance four core value areas: 1) Scientific Expertise; 2) Innovations; 3) Mentoring and Diversity; and 4) Network Development. To complement the ongoing research activities of both the diagnostic and the pharmaceutical industries, our ARLG has established collaborative ties with members of both communities. Our long-term research goal is to improve outcomes of multiple-drug resistant (MDR) bacterial infections by designing and conducting transformational diagnostic and therapeutic clinical trials. Our research portfolio will pursue this goal in therapeutics by conducting first-in kind strategy trials in MDR Gram-negative bacteria and MRSA and by studying nontraditional therapeutics (monoclonal antibodies and bacteriophages) against MDR Pseudomonas aeruginosa. We will pursue this goal in diagnostics by obtaining FDA approval for a host gene expression-based diagnostic and by evaluating the clinical impact of rapid phenotypic testing in patients with bloodstream infection. Our research agenda reflects a realistic strategy of incremental steps towards complex practice-changing trials. Our Specific Aims are to 1) To maintain a Scientific Leadership Center (SLC) that provides overall scientific and administrative leadership for the network; 2) To maintain a Clinical Operations Center (COC) that provides operational support, management, and oversight for the network’s clinical studies and trials; 3) To maintain a Laboratory Center (LC) that advances the ARLG research agenda by leading the development, implementation, and evaluation of essential laboratory research; and 4): To maintain a Statistics and Data Management Center (SDMC) that advances the ARLG research agenda by providing leadership in biostatistics, study design, analysis, interpretation, and publication of results. By advancing these specific aims, our renewal will build upon the productivity and innovation assembled in our original award to advance the ARLG scientific agenda against one of the leading threats to human health.
我们的目标是继续推进抗菌药物的成功,多学科研究议程

项目成果

期刊论文数量(0)
专著数量(0)
科研奖励数量(0)
会议论文数量(0)
专利数量(0)

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Vance G. Fowler其他文献

Inflammasome-mediated glucose limitation induces antibiotic tolerance in emStaphylococcus aureus/em
炎症小体介导的葡萄糖限制诱导金黄色葡萄球菌产生抗生素耐受性
  • DOI:
    10.1016/j.isci.2023.107942
  • 发表时间:
    2023-10-20
  • 期刊:
  • 影响因子:
    4.100
  • 作者:
    Jenna E. Beam;Nikki J. Wagner;Kuan-Yi Lu;Joshua B. Parsons;Vance G. Fowler;Sarah E. Rowe;Brian P. Conlon
  • 通讯作者:
    Brian P. Conlon
Impact of neutropenia on clinical manifestations and outcome of emStaphylococcus aureus/em bloodstream infection: a propensity score-based overlap weight analysis in two large, prospectively evaluated cohorts
中性粒细胞减少症对金黄色葡萄球菌血流感染临床表现和结局的影响:基于倾向评分的重叠权重分析在两个大型前瞻性评估队列中的应用
  • DOI:
    10.1016/j.cmi.2022.03.018
  • 发表时间:
    2022-08-01
  • 期刊:
  • 影响因子:
    8.500
  • 作者:
    Johannes Camp;Tim Filla;Lina Glaubitz;Achim J. Kaasch;Frieder Fuchs;Matt Scarborough;Hong Bin Kim;Robert Tilley;Chun-Hsing Liao;Jonathan Edgeworth;Emmanuel Nsutebu;Luis Eduardo López-Cortés;Laura Morata;Martin J. Llewelyn;Vance G. Fowler;Guy Thwaites;Harald Seifert;Winfried V. Kern;Siegbert Rieg;INSTINCT and ISAC study groups;the ESCMID Study Group for Bloodstream Infections, Endocarditis and Sepsis
  • 通讯作者:
    the ESCMID Study Group for Bloodstream Infections, Endocarditis and Sepsis
Redefining emStaphylococcus aureus/em bacteremia: A structured approach guiding diagnostic and therapeutic management
重新定义金黄色葡萄球菌菌血症:一种指导诊断和治疗管理的结构化方法
  • DOI:
    10.1016/j.jinf.2022.10.042
  • 发表时间:
    2023-01-01
  • 期刊:
  • 影响因子:
    11.900
  • 作者:
    Ilse J.E. Kouijzer;Vance G. Fowler;Jaap ten Oever
  • 通讯作者:
    Jaap ten Oever
Methicillin-resistant Staphylococcus aureus: an overview of basic and clinical research
耐甲氧西林金黄色葡萄球菌:基础与临床研究概述
  • DOI:
    10.1038/s41579-018-0147-4
  • 发表时间:
    2019-02-08
  • 期刊:
  • 影响因子:
    103.300
  • 作者:
    Nicholas A. Turner;Batu K. Sharma-Kuinkel;Stacey A. Maskarinec;Emily M. Eichenberger;Pratik P. Shah;Manuela Carugati;Thomas L. Holland;Vance G. Fowler
  • 通讯作者:
    Vance G. Fowler
All emStaphylococcus aureus/em bacteraemia-inducing strains can cause infective endocarditis: Results of GWAS and experimental animal studies
所有金黄色葡萄球菌致菌血症菌株均可引起感染性心内膜炎:全基因组关联研究和实验动物研究结果
  • DOI:
    10.1016/j.jinf.2022.12.028
  • 发表时间:
    2023-02-01
  • 期刊:
  • 影响因子:
    11.900
  • 作者:
    Sylvère Bastien;Severien Meyers;Wilmara Salgado-Pabón;Stefano G. Giulieri;Jean-Phillipe Rasigade;Laurens Liesenborghs;Kyle J. Kinney;Florence Couzon;Patricia Martins-Simoes;Vincent Le Moing;Xavier Duval;Natasha E Holmes;Niels Eske Bruun;Robert Skov;Benjamin P Howden;Vance G. Fowler;Peter Verhamme;Paal Skytt Andersen;Coralie Bouchiat;Karen Moreau;François Vandenesch
  • 通讯作者:
    François Vandenesch

Vance G. Fowler的其他文献

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{{ truncateString('Vance G. Fowler', 18)}}的其他基金

HLA Fine Mapping to Elucidate S. aureus Susceptibility
HLA 精细作图阐明金黄色葡萄球菌敏感性
  • 批准号:
    10490895
  • 财政年份:
    2021
  • 资助金额:
    $ 1472.99万
  • 项目类别:
HLA Fine Mapping to Elucidate S. aureus Susceptibility
HLA 精细作图阐明金黄色葡萄球菌敏感性
  • 批准号:
    10344003
  • 财政年份:
    2021
  • 资助金额:
    $ 1472.99万
  • 项目类别:
2013 Staphylococcal Diseases Gordon Research Conference and Gordon Research Semin
2013年葡萄球菌疾病戈登研究会议及戈登研究研讨会
  • 批准号:
    8526118
  • 财政年份:
    2013
  • 资助金额:
    $ 1472.99万
  • 项目类别:
Antibacterial Resistance Leadership Group (ARLG)
抗菌素耐药性领导小组 (ARLG)
  • 批准号:
    10064119
  • 财政年份:
    2013
  • 资助金额:
    $ 1472.99万
  • 项目类别:
Antibacterial Resistance Leadership Group (ARLG)
抗菌素耐药性领导小组 (ARLG)
  • 批准号:
    10247231
  • 财政年份:
    2013
  • 资助金额:
    $ 1472.99万
  • 项目类别:
Antibacterial Resistance Leadership Group (ARLG)
抗菌素耐药性领导小组 (ARLG)
  • 批准号:
    8667988
  • 财政年份:
    2013
  • 资助金额:
    $ 1472.99万
  • 项目类别:
Antibacterial Resistance Leadership Group (ARLG)
抗菌素耐药性领导小组 (ARLG)
  • 批准号:
    8776915
  • 财政年份:
    2013
  • 资助金额:
    $ 1472.99万
  • 项目类别:
Antibacterial Resistance Leadership Group (ARLG)
抗菌素耐药性领导小组 (ARLG)
  • 批准号:
    8478367
  • 财政年份:
    2013
  • 资助金额:
    $ 1472.99万
  • 项目类别:
Antibacterial Resistance Leadership Group (ARLG)
抗菌素耐药性领导小组 (ARLG)
  • 批准号:
    8975602
  • 财政年份:
    2013
  • 资助金额:
    $ 1472.99万
  • 项目类别:
Antibacterial Resistance Leadership Group (ARLG)
抗菌素耐药性领导小组 (ARLG)
  • 批准号:
    10542803
  • 财政年份:
    2013
  • 资助金额:
    $ 1472.99万
  • 项目类别:

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