GRADS Clinical Center: Studies in Sarcoidosis and Microbiomics Research

GRADS 临床中心:结节病和微生物组学研究

基本信息

  • 批准号:
    8662312
  • 负责人:
  • 金额:
    $ 15.68万
  • 依托单位:
  • 依托单位国家:
    美国
  • 项目类别:
  • 财政年份:
    2012
  • 资助国家:
    美国
  • 起止时间:
    2012-05-01 至 2016-04-30
  • 项目状态:
    已结题

项目摘要

DESCRIPTION (provided by applicant): Sarcoidosis is a granulomatous inflammatory disease of great clinical importance, yet its etiology and pathogenesis remain incompletely understood. Both host and environmental factors are believed to be involved. Newly emerging scientific approaches in immunology, gene expression and other areas offer significant promise to reveal new insight into the disease and identify potential new treatments. GRADS is a multicenter program for recruitment of subjects and biospecimen collection to enable application of these techniques. Our group has been involved in several previous multicenter studies of sarcoid, with a demonstrated record of recruitment, clinical phenotyping, and specimen contribution. The overall goal of our project is to contribute to subject recruitment, high quality phenotyping and biospecimen collection for applying these new technologies through the GRADS consortium. Considerable evidence implicates an infectious trigger in sarcoid pathogenesis, but prior studies have been unrevealing or inconsistent. Recent advances in culture-independent molecular microbiology are revealing unexpected insights into complex microbial populations and their nature in human health and disease. These approaches do not require ability to culture or a priori knowledge of microbial agents. Our group has pioneered the use of these approaches to define complex bacterial and viral populations in gut and blood. In addition, through a new program in respiratory tract microbiomics, we have developed novel high stringency sampling, analytic and bioinformatic approaches to overcome important challenges in applying these approaches to the lung, and demonstrated the ability to molecularly define genuine lower respiratory tract microbial inhabitants, and identify unique lung microbes distinct from upper respiratory tract or environmental sources. Our center-specific project hypothesis is that microbial agents contribute to the pathogenesis of sarcoidosis and can be identified through culture-independent molecular approaches utilizing stringent sample collection and novel bioinformatic tools. This proposal reflects a new, synergistic collaboration that takes advantage of established infrastructure and expertise on campus in clinical research and sarcoid pathogenesis (Rossman & Kreider) and a recently-established innovative program in respiratory tract microbiome studies (Collman & Bushman). Our specific aims are to: (1) Enroll subjects with newly diagnosed sarcoidosis for detailed clinical phenotyping and high quality biospecimen collection for consortium wide study goals: (2) Carry out a center-specific study to define the culture-independent microbial populations in the lower respiratory tract of sarcoid (stage 2) and control subiects utilizing high stringency sampling and pyrosequencing including bacterial 16S ribosomal rRNA gene, microeukaryote rRNA gene and virome metagenomic approaches; and (3) Participate in study-wide protocols as developed by the Steering Committee and NIH program and, if supported by group goals, facilitate microbiome analysis on consortium-wide samples via procedures established through the GIC. RELEVANCE: The cause of Sarcoid is unknown but new approaches in immunology, gene expression and other areas may reveal new insight and identify new treatments. We have been involved in multicenter studies of sarcoid with a strong record of recruitment and specimen contribution, and we will recruit subjects and contribute specimens for GRADS. Many lines of evidence suggest a possible infectious trigger, but prior studies are contradictory. New molecular microbiology approaches have revolutionized studies of microbes in the body, and our group has pioneered their application to the lung. Our Center Project will apply this new technology to identify possible infectious agents associated with sarcoid.
描述(由申请人提供):

项目成果

期刊论文数量(1)
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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Ronald G Collman其他文献

Low levels of SIV infection in sooty mangabey central memory CD4+ T cells are associated with limited CCR5 expression
黑长尾猴中央记忆 CD4+T 细胞中低水平的 SIV 感染与有限的 CCR5 表达相关。
  • DOI:
    10.1038/nm.2395
  • 发表时间:
    2011-06-26
  • 期刊:
  • 影响因子:
    50.000
  • 作者:
    Mirko Paiardini;Barbara Cervasi;Elane Reyes-Aviles;Luca Micci;Alexandra M Ortiz;Ann Chahroudi;Carol Vinton;Shari N Gordon;Steven E Bosinger;Nicholas Francella;Paul L Hallberg;Elizabeth Cramer;Timothy Schlub;Ming Liang Chan;Nadeene E Riddick;Ronald G Collman;Cristian Apetrei;Ivona Pandrea;James Else;Jan Munch;Frank Kirchhoff;Miles P Davenport;Jason M Brenchley;Guido Silvestri
  • 通讯作者:
    Guido Silvestri
The enigmatic roles of emAnelloviridae/em and emRedondoviridae/em in humans
人类中的 emAnelloviridae/em 和 emRedondoviridae/em 的神秘作用
  • DOI:
    10.1016/j.coviro.2022.101248
  • 发表时间:
    2022-08-01
  • 期刊:
  • 影响因子:
    5.100
  • 作者:
    Louis J Taylor;Emma L Keeler;Frederic D Bushman;Ronald G Collman
  • 通讯作者:
    Ronald G Collman
Erratum: Longer hospital stay is associated with high rates of tuberculosis-related morbidity and mortality within 12 months after discharge in a referral hospital in Sub-Saharan Africa
  • DOI:
    10.1186/s12879-015-0942-8
  • 发表时间:
    2015-05-10
  • 期刊:
  • 影响因子:
    3.000
  • 作者:
    Nicola M Zetola;Nenad Macesic;Sanghyuk S Shin;Alexandra Peloso;Ronald Ncube;Jeffrey D Klausner;Chawangwa Modongo;Ronald G Collman
  • 通讯作者:
    Ronald G Collman

Ronald G Collman的其他文献

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{{ truncateString('Ronald G Collman', 18)}}的其他基金

The Oropharyngeal Microbiome in COVID-19
COVID-19 中的口咽微生物组
  • 批准号:
    10592682
  • 财政年份:
    2023
  • 资助金额:
    $ 15.68万
  • 项目类别:
Epigenetic HIV Silencing in Macrophages
巨噬细胞中的表观遗传 HIV 沉默
  • 批准号:
    10205406
  • 财政年份:
    2017
  • 资助金额:
    $ 15.68万
  • 项目类别:
Epigenetic HIV Silencing in Macrophages
巨噬细胞中的表观遗传 HIV 沉默
  • 批准号:
    10231275
  • 财政年份:
    2017
  • 资助金额:
    $ 15.68万
  • 项目类别:
GRADS Clinical Center: Studies in Sarcoidosis and Microbiomics Research
GRADS 临床中心:结节病和微生物组学研究
  • 批准号:
    8464263
  • 财政年份:
    2012
  • 资助金额:
    $ 15.68万
  • 项目类别:
GRADS Clinical Center: Studies in Sarcoidosis and Microbiomics Research
GRADS 临床中心:结节病和微生物组学研究
  • 批准号:
    8264679
  • 财政年份:
    2012
  • 资助金额:
    $ 15.68万
  • 项目类别:
Entry Coreceptor Use & Target Cell Tropism in Nonpathogenic SIV Infection
进入辅助受体的使用
  • 批准号:
    8261785
  • 财政年份:
    2011
  • 资助金额:
    $ 15.68万
  • 项目类别:
Viral & Molecular
病毒性的
  • 批准号:
    7684970
  • 财政年份:
    2009
  • 资助金额:
    $ 15.68万
  • 项目类别:
Core--Viral, Cellular and Molecular Biology Facility
核心——病毒、细胞和分子生物学设施
  • 批准号:
    7650389
  • 财政年份:
    2008
  • 资助金额:
    $ 15.68万
  • 项目类别:
Core--Viral, Cellular and Molecular Biology Facility
核心——病毒、细胞和分子生物学设施
  • 批准号:
    7456544
  • 财政年份:
    2007
  • 资助金额:
    $ 15.68万
  • 项目类别:
Gp120, Macrophage Activation & TNF in HIV Encephalopathy
Gp120,巨噬细胞激活
  • 批准号:
    7016244
  • 财政年份:
    2005
  • 资助金额:
    $ 15.68万
  • 项目类别:

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