2010 Molecular Biology of Hepatitis B Viruses Meeting

2010年乙型肝炎病毒分子生物学会议

基本信息

  • 批准号:
    7915035
  • 负责人:
  • 金额:
    $ 1.8万
  • 依托单位:
  • 依托单位国家:
    美国
  • 项目类别:
  • 财政年份:
    2010
  • 资助国家:
    美国
  • 起止时间:
    2010-08-01 至 2011-07-31
  • 项目状态:
    已结题

项目摘要

DESCRIPTION (provided by applicant): Approximately 25% of the earth's population, 2 billion people, have been infected by Hepatitis B Virus (HBV). Approximately 360 million people suffer from chronic infection. Chronic HBV contributes to the deaths of some 600,000 people annually mainly by liver failure, cirrhosis, and hepatocellular carcinoma. In addition to significant morbidity, acute HBV infection is correlated with pancreatic cancer. Approximately 15 million HBV victims are co-infected with Hepatitis Delta Virus, which can increase the chance of liver failure and cancer. New infections continue to arise, despite the availability of a vaccine, due to the ~10% non-response rate and underutilization of the vaccine due to cost and other issues. For those with chronic HBV the vaccine is not therapeutic. The available antiviral approaches are expensive, rarely clear the infection, and can lead to a serious rebound when therapy is terminated. This proposal requests funds to support the 2010 Molecular Biology of Hepatitis B Viruses Meeting to be held in Taipei, Taiwan from October 9 -13, 2010. The Hepatitis B meeting is a forum for the truly international community of researchers focusing on HBV and the closely associated HDV. For the first time this meeting will be held in Southeast Asia, where as much as 20% of the population has chronic HBV. 2010 will mark the 25th anniversary of the first HBV meeting, organized by Harold Varmus and Jesse Summers. Since then, the HBV meeting has introduced a continuous series of broad-reaching advances to the virology community. Because so much scientific progress arises from competition, collaboration, and discussion, it can be argued that the HBV meeting has contributed to these advances. It is, therefore, imperative that basic research and the scientific exchange among those studying HBV/HDV continue and the annual HBV meeting represents the venue at which this can occur. The 2010 meeting will continue in this tradition by emphasizing discussion and networking in two poster sessions, 10 oral sessions, a workshop on the structural biology of hepadnaviruses, and keynote addresses on innate immune response and spumaviridae (a retrovirus genus with some distinctly HBV-like properties). Because of its location, a great effort has been made to minimize the cost of the meeting by working with the Academia Sinica campus. Furthermore, the Hepatitis B Foundation which has administratively supported this meeting since 2005, making its staff available for organizing the meeting and publicizing it, especially to universities with large numbers of underrepresented minorities. In order to allow the participation of junior and minority investigators, support from the NIH to help defray the meeting costs of junior scientists is requested. Limited support for meeting materials and organizational functions is also needed. The 2010 Molecular Biology of Hepatitis B Viruses Meeting, the 26th in the series, is the definitive meeting that brings together basic scientists in the field of Hepatitis B Virus (HBV) and Hepatitis Delta Virus (HDV) from around the world. HBV is a major global and US public health problem with approximately 2 billion individuals infected by HBV, 360 million chronically, resulting in an annual rate of approximately 600,000 deaths due to HBV and HBV/HDV-induced liver failure, cirrhosis, and hepatocellular carcinoma. The meeting is a critical and internationally well-recognized platform for exchange of information in basic research on HBV and HDV infections.
描述(由申请人提供):大约25%的地球人口,20亿人,已经感染了B肝炎病毒(HBV)。约有3.6亿人患有慢性感染。慢性HBV导致每年约600,000人死亡,主要是肝衰竭、肝硬化和肝细胞癌。除了显著的发病率,急性HBV感染与胰腺癌相关。大约有1500万HBV患者同时感染了丁型肝炎病毒,这会增加肝衰竭和癌症的机会。尽管有疫苗可供使用,但由于约10%的无应答率以及由于成本和其他问题而导致的疫苗利用不足,新的感染继续出现。对于慢性HBV感染者,疫苗不具有治疗作用。可用的抗病毒方法是昂贵的,很少清除感染,并可能导致严重的反弹时,治疗终止。该提案要求提供资金以支持将于2010年10月9日至13日在台湾台北举行的2010年B型肝炎病毒分子生物学会议。B型肝炎会议是一个真正的国际社会的研究人员集中在HBV和密切相关的HDV的论坛。该会议将首次在东南亚举行,那里多达20%的人口患有慢性HBV。2010年将是由Harold Varmus和Jesse Summers组织的第一次HBV会议25周年。从那时起,HBV会议向病毒学界介绍了一系列持续的广泛进展。由于如此多的科学进步来自竞争、合作和讨论,因此可以说HBV会议为这些进步做出了贡献。因此,基础研究和HBV/HDV研究人员之间的科学交流必须继续下去,年度HBV会议是可能发生这种情况的场所。2010年的会议将继续这一传统,强调讨论和网络在两个海报会议,10个口头会议,嗜肝DNA病毒的结构生物学研讨会,以及关于先天免疫反应和逆转录病毒科(一种逆转录病毒属,具有一些明显的HBV样特性)的主旨演讲。由于地理位置的关系,我们与中央研究院合作,尽量减少会议的费用。此外,B型肝炎基金会自2005年以来一直在行政上支持这一会议,为组织会议和宣传会议提供了工作人员,特别是向少数群体代表人数不足的大学提供了工作人员。为了让初级和少数民族的研究人员参与,从美国国立卫生研究院的支持,以帮助支付会议费用的初级科学家被要求。还需要对会议材料和组织职能提供有限的支助。2010年B型肝炎病毒分子生物学会议是该系列会议的第26届,是汇集了来自世界各地的B型肝炎病毒(HBV)和丁型肝炎病毒(HDV)领域的基础科学家的权威会议。HBV是全球和美国的主要公共卫生问题,约有20亿人感染HBV,其中3.6亿人慢性感染,每年约有60万人死于HBV和HBV/HDV诱导的肝衰竭、肝硬化和肝细胞癌。该会议是一个重要的和国际公认的平台,用于交流HBV和HDV感染基础研究的信息。

项目成果

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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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Adam Zlotnick其他文献

Adam Zlotnick的其他文献

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{{ truncateString('Adam Zlotnick', 18)}}的其他基金

The Structural Biology of HBV
乙型肝炎病毒的结构生物学
  • 批准号:
    10117172
  • 财政年份:
    2019
  • 资助金额:
    $ 1.8万
  • 项目类别:
The Structural Biology of HBV
乙型肝炎病毒的结构生物学
  • 批准号:
    9899197
  • 财政年份:
    2019
  • 资助金额:
    $ 1.8万
  • 项目类别:
The Structural Biology of HBV
乙型肝炎病毒的结构生物学
  • 批准号:
    10372082
  • 财政年份:
    2019
  • 资助金额:
    $ 1.8万
  • 项目类别:
Multimode Observation of Virus Capsid Assembly
病毒衣壳组装的多模式观察
  • 批准号:
    9116986
  • 财政年份:
    2016
  • 资助金额:
    $ 1.8万
  • 项目类别:
Multimode Observation of Virus Capsid Assembly
病毒衣壳组装的多模式观察
  • 批准号:
    9900731
  • 财政年份:
    2016
  • 资助金额:
    $ 1.8万
  • 项目类别:
Multimode Observation of Virus Capsid Assembly
病毒衣壳组装的多模式观察
  • 批准号:
    10587218
  • 财政年份:
    2016
  • 资助金额:
    $ 1.8万
  • 项目类别:
The Biophysics of Virus Capsid Assembly
病毒衣壳组装的生物物理学
  • 批准号:
    8880573
  • 财政年份:
    2014
  • 资助金额:
    $ 1.8万
  • 项目类别:
Assembly of a Dodecahedral Virus
十二面体病毒的组装
  • 批准号:
    8600240
  • 财政年份:
    2013
  • 资助金额:
    $ 1.8万
  • 项目类别:
Assembly of a Dodecahedral Virus
十二面体病毒的组装
  • 批准号:
    8415339
  • 财政年份:
    2013
  • 资助金额:
    $ 1.8万
  • 项目类别:
STRUCTURAL BASIS OF CONTROLLING VIRUS CAPSID ASSEMBLY
控制病毒衣壳组装的结构基础
  • 批准号:
    8171995
  • 财政年份:
    2010
  • 资助金额:
    $ 1.8万
  • 项目类别:

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ISARIC CCP activation for acute hepatitis of unknown cause
ISARIC CCP 激活治疗不明原因急性肝炎
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  • 财政年份:
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Neutralizing antibody responses during natural control of acute hepatitis B with and without HIV-1 coinfection
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  • 批准号:
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  • 财政年份:
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Neutralizing antibody responses during natural control of acute hepatitis B with and without HIV-1 coinfection
在有或没有 HIV-1 合并感染的急性乙型肝炎自然控制过程中中和抗体反应
  • 批准号:
    10674691
  • 财政年份:
    2022
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    $ 1.8万
  • 项目类别:
Biomarkers of spontaneous acute hepatitis C virus resolution
自发性急性丙型肝炎病毒消退的生物标志物
  • 批准号:
    8262303
  • 财政年份:
    2012
  • 资助金额:
    $ 1.8万
  • 项目类别:
Biomarkers of spontaneous acute hepatitis C virus resolution
自发性急性丙型肝炎病毒消退的生物标志物
  • 批准号:
    8458955
  • 财政年份:
    2012
  • 资助金额:
    $ 1.8万
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Effects of Vitamin E Derevative , ETS-GS for the treatment of acute hepatitis
维生素E衍生物ETS-GS治疗急性肝炎的疗效
  • 批准号:
    23592260
  • 财政年份:
    2011
  • 资助金额:
    $ 1.8万
  • 项目类别:
    Grant-in-Aid for Scientific Research (C)
Investigation the mechanisms of chronicity from acute hepatitis B using a next generation sequencer
使用下一代测序仪研究急性乙型肝炎的慢性机制
  • 批准号:
    22790679
  • 财政年份:
    2010
  • 资助金额:
    $ 1.8万
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    Grant-in-Aid for Young Scientists (B)
Baltimore Acute Hepatitis C Cooperative Center
巴尔的摩急性丙型肝炎合作中心
  • 批准号:
    8625266
  • 财政年份:
    2010
  • 资助金额:
    $ 1.8万
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Mechanisms of repeated control of acute hepatitis C infection in humans
反复控制人类急性丙型肝炎感染的机制
  • 批准号:
    9900734
  • 财政年份:
    2010
  • 资助金额:
    $ 1.8万
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Baltimore Acute Hepatitis C Cooperative Center
巴尔的摩急性丙型肝炎合作中心
  • 批准号:
    8240544
  • 财政年份:
    2010
  • 资助金额:
    $ 1.8万
  • 项目类别:
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