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38th Annual Symposium on Nonhuman Primate Models for AIDS

38th Annual Symposium on Nonhuman Primate Models for AIDS
第38届非人类灵长类艾滋病模型年度研讨会
批准号:
10012735
负责人:
Nancy L Haigwood
金额:
$7.5万
依托单位国家:
美国
项目类别:
财政年份:
2020
资助国家:
美国
项目状态:
已结题
起止时间:
2020-03-01 至 2022-02-28

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中文摘要
翻译
项目总结 通过此R13应用程序,我们请求资金部分支持计划、组织、宣传、 并主办第38届艾滋病非人类灵长类模型年度研讨会。这次研讨会将是 由俄勒冈州国家灵长类研究中心(ONPRC)主办。它将在位于北京的九号酒店举行。 俄勒冈州波特兰市中心,2020年9月29日至10月2日。住宿将在同一地点提供。在……里面 除了此R13提案中要求的资金外,支持将来自会议支付的注册费 参与者和来自企业赞助商的贡献。会议的总体形式将从 登记和9月29日的晚间招待会,随后将发表主旨演讲 多尔蒂研究所所长、墨尔本大学医学教授莎伦·勒文博士说。那里 将进行为期两天半的科学演讲,由受邀演讲者和接受的口头演讲共同推动 摘要。招贴会将在9月30日晚上举行,暂定将举行宴会 计划于10月1日在波特兰美术馆举行。本次会议的主要重点将是 可以推进艾滋病NHP模型研究的技术。基于这一主题,会议主题和 将邀请演讲者重点介绍各自领域的新技术和尖端技术。每节课 将以一位特邀主席25分钟的演讲开始。剩下的讲座将由以下个人进行 根据提交材料的质量和原创性,接受摘要作口头陈述。会有的 为无法在口头会议中容纳的有功绩的摘要提供晚间海报会议。AS 所有海报和口头摘要都将发表在《医学杂志》上 灵长类动物学。ONPRC还将在以下时间为早期调查人员(ESI)主持一次研讨会前会议 9月29日,与艾滋病毒疫苗试验网络主办的翻译ESI会议相结合 (HVTN)将于9月28日至29日在俄勒冈州波特兰举行。此会议将向以下组织的与会者开放 由HVTN主办的关联ESI会议。ESI与会者和导师将制定一项计划 专注于网络、拨款撰写、预算和与NIH项目官员的问答。总的来说,主要的 年度研讨会的目的是帮助传播NHP艾滋病模型的最新研究成果, 同时还营造了一种环境,促进基本人员之间的讨论和思想交流 科学家和临床医生之间,以及早期和成熟的研究人员之间。我们相信,带着 来自各种不同背景的研究人员将共同推动未来的合作。总而言之,我们 希望第38届艾滋病非人类灵长类动物模型研讨会有助于确定最有效的 利用国家惠普模式更好地设计干预措施,以预防或根除艾滋病毒感染或保持长期 在没有抗逆转录病毒治疗的情况下控制艾滋病毒复制。
英文摘要
PROJECT SUMMARY With this R13 application we request funding to support, in part, the costs for planning, organizing, publicizing, and hosting the 38th Annual Symposium on Nonhuman Primate Models for AIDS. This symposium will be hosted by the Oregon National Primate Research Center (ONPRC). It will be held at “The Nines” hotel located in downtown Portland, Oregon, September 29 - October 2, 2020. Lodging will be offered at the same venue. In addition to the funds requested in this R13 proposal, support will come from registration fees paid by meeting participants and contributions from corporate sponsors. The overall format of the conference will begin with registration and an evening reception on September 29, which will be followed by a keynote address given by Dr. Sharon Lewin, Director of the Doherty Institute and Professor of Medicine, University of Melbourne. There will be two and a half days of scientific presentations driven by both invited speakers and accepted oral abstracts. A poster session will occur on the evening of September 30, and there will be a banquet, tentatively planned for The Portland Art Museum on October 1. A major emphasis for this meeting will be on emerging technologies that can advance research in NHP models of AIDS. Based on this theme, session topics and speakers will be invited to highlight new and cutting-edge technologies in their respective fields. Each session will open with a 25-minute talk by an invited Chair. Remaining session talks will be given by individuals whose abstracts were accepted for oral presentations based on the quality and originality of the submission. There will be an evening poster session for meritorious abstracts that cannot be accommodated in the oral sessions. As is customary for this symposium, all poster and oral abstracts will be published in the Journal of Medical Primatology. ONPRC will also be hosting a pre-symposium meeting for early stage investigators (ESI) on September 29 in conjunction with a Translational ESI conference sponsored by the HIV Vaccine Trials Network (HVTN) to be held September 28-29 in Portland, Oregon. This meeting will be open to the attendees of a linked ESI Conference sponsored by the HVTN. The ESI attendees and mentors will develop a program focused on networking, grant writing, budgeting and a Q&A with NIH Program Officers. In general, the main objective of the annual symposium is to help disseminate the latest research findings in NHP models of AIDS, while also fostering an environment that will facilitate discussion and exchange of ideas between basic scientists and clinicians, as well as between early stage and established investigators. We believe that bringing together researchers from a wide variety of different backgrounds will generate future collaborations. In all, we hope that the 38th Annual Nonhuman Primate Models for AIDS Symposium will help identify the most effective use of NHP models to better design interventions to prevent or eradicate HIV infection or to maintain long term control of HIV replication in the absence of antiretroviral therapy.
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