Macaque Resources
猕猴资源
基本信息
- 批准号:7663388
- 负责人:
- 金额:--
- 依托单位:
- 依托单位国家:美国
- 项目类别:
- 财政年份:2009
- 资助国家:美国
- 起止时间:2009-07-16 至 2014-06-30
- 项目状态:已结题
- 来源:
- 关键词:Acquired Immunodeficiency SyndromeAnimal ModelAnimalsAntibodiesAntigensArtsBiological AssayBloodBudgetsCD8B1 geneCellsCellular ImmunologyComplexDiseaseEnsureFlow CytometryGoalsHIVHIV vaccineHumanHuman ResourcesImmune responseImmune systemImmunityImmunologic MonitoringInfection preventionInstructionInvestigationMacacaMacaca mulattaModelingOregonPrimatesProtocols documentationResearchResearch DesignResearch InfrastructureResearch PersonnelResourcesSIVSamplingStructureT-LymphocyteTechnical ExpertiseTissuesVaccinationVaccine ResearchVaccinesVirus Diseasesanimal carecytokineexperienceimmunogenicitymeetingsneutralizing antibodynonhuman primatepandemic diseasepre-clinicalprogramssimian human immunodeficiency virusvaccine development
项目摘要
The Indian rhesus macaque develops a disease that closely mimics human acquired immunodeficiency
syndrome (AIDS) when infected by simian immunodeficiency virus (SIV) or chimeric simian-human
immunodeficiency viruses (SHIV), and represents the best animal model for HIV infection. Because of the
similarity of the immune systems of macaques and humans, preclinical vaccine development is heavily
dependent on the SIV and SHIV macaque models. Their research value notwithstanding, nonhuman
primates (NHPs) are complex, higher order species that require specialized infrastructure and expertise in a
research setting. The NHP Core seeks to consolidate the experimental animal and cellular immunology
portions of the HIV Vaccine Research and Design (HIVRAD) Program project, "Programming HIV Immune
Response for Broadly Neutralizing Antibodies by Vaccination" into a single Core composed of highly
experienced professional and technical personnel and state-of-the-art resources. The NHP Core, functioning
within the Oregon National Primate Research Center (ONPRC), will provide infrastructure and professional
and technical expertise for the NHP experimental protocol and the antigen (Ag)-specific CD4+ and CD8+ T
cell analyses supporting the "HIV Quasispecies Vaccine Immunogenicity and SHIV Challenge Study". The
Specific Aims are: 1) to provide specialized expertise and infrastructure for comprehensive, efficient and safe
conduct of the nonhuman primate-related portions of the HIVRAD Program including animal selection,
research protocol implementation and execution, sample acquisition and distribution, animal care, and
project budget administration, and 2) to provide the HIVRAD Program with flow cytometric assays of Ag-
specific T cell immunity and SHIV immunopathogenesis. The immune monitoring section of the Nonhuman
Primate Core will provide sophisticated assays of SIV/HIV-specific T cell immunity (polychromatic cytokine
flow cytometry) and SHIV immunopathogenesis (polychromatic phenotypic analysis) of SHIV target cell
dynamics in blood and tissue.
RELEVANCE (See instructions):
A safe and effective vaccine remains the best hope of controlling the human immunodeficiency virus (HIV)
pandemic. The studies in this proposal focus on developing vaccine strategies to promote broadly
neutralizing anti-HIV antibody, a key component of the host immune response against HIV that may prevent
infection.
印度恒河猴患上一种与人类获得性免疫缺陷极为相似的疾病
当被猴免疫缺陷病毒(SIV)或嵌合猴-人感染时,
免疫缺陷病毒(SHIV),并代表了最好的动物模型的HIV感染。因为
由于猕猴和人类免疫系统的相似性,临床前疫苗的开发在很大程度上
依赖于SIV和SHIV猕猴模型。尽管它们有研究价值,
灵长类动物(NHP)是复杂的高阶物种,需要专门的基础设施和专业知识,
研究设置。NHP核心旨在巩固实验动物和细胞免疫学
艾滋病毒疫苗研究与设计(HIVRAD)计划项目“艾滋病毒免疫程序设计“的部分内容
通过疫苗接种对广泛中和抗体的反应”的核心,
经验丰富的专业技术人员和最先进的资源。NHP核心,运行
在俄勒冈州国家灵长类动物研究中心(ONPRC),将提供基础设施和专业
NHP实验方案和抗原(Ag)特异性CD 4+和CD 8 + T细胞
支持“HIV准种疫苗免疫原性和SHIV攻毒研究”的细胞分析。的
具体目标是:1)提供专业知识和基础设施,
开展HIVRAD计划中与非人灵长类动物相关的部分,包括动物选择,
研究方案的实施和执行,样本采集和分发,动物护理,以及
项目预算管理,以及2)为HIVRAD计划提供流式细胞术检测Ag-
特异性T细胞免疫和SHIV免疫发病机制。非人免疫监测部分
Primate Core将提供SIV/HIV特异性T细胞免疫(多色细胞因子)的复杂检测
流式细胞术)和SHIV免疫发病机制(多色表型分析)的SHIV靶细胞
血液和组织中的动力学。
相关性(参见说明):
一种安全有效的疫苗仍然是控制人类免疫缺陷病毒(艾滋病毒)的最大希望
流行病本提案中的研究重点是制定疫苗战略,
中和性抗HIV抗体是宿主对HIV免疫反应的关键成分,
感染
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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Louis J. Picker其他文献
760. Overcoming Rhesus Macaque Endogenous Restriction Factors during HIV-1 Vector Transduction
- DOI:
10.1016/j.ymthe.2006.08.844 - 发表时间:
2006-01-01 - 期刊:
- 影响因子:
- 作者:
Christina H. Swan;Udayan Chatterji;Philippe Gallay;Louis J. Picker;Bruce E. Torbett - 通讯作者:
Bruce E. Torbett
Pulmonary Artery-Bronchial Fistula Complicating Chronic Lymphocytic Leukemia
- DOI:
10.1378/chest.86.1.134 - 发表时间:
1984-07-01 - 期刊:
- 影响因子:
- 作者:
James K. Stoller;Louis J. Picker;Scott T. Weiss;Robert L. Thurer;Earl J. Kasdon - 通讯作者:
Earl J. Kasdon
Antibodies advance the search for a cure
抗体推动了对治愈方法的探索
- DOI:
10.1038/nature12703 - 发表时间:
2013-10-30 - 期刊:
- 影响因子:48.500
- 作者:
Louis J. Picker;Steven G. Deeks - 通讯作者:
Steven G. Deeks
Seeking ultimate victory
追求最终的胜利
- DOI:
10.1038/nature14194 - 发表时间:
2015-01-07 - 期刊:
- 影响因子:48.500
- 作者:
Louis J. Picker;Jeffrey D. Lifson - 通讯作者:
Jeffrey D. Lifson
Programming cytomegalovirus as an HIV vaccine
将巨细胞病毒编程为一种 HIV 疫苗
- DOI:
10.1016/j.it.2023.02.001 - 发表时间:
2023-04-01 - 期刊:
- 影响因子:13.900
- 作者:
Louis J. Picker;Jeffrey D. Lifson;Michael Gale;Scott G. Hansen;Klaus Früh - 通讯作者:
Klaus Früh
Louis J. Picker的其他文献
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{{ truncateString('Louis J. Picker', 18)}}的其他基金
Project 1: Systemic analysis of the origin and tissue effects of the 68-1 RhCMV/SIV vaccine efficacy-predictive whole blood transcriptomic signature
项目1:68-1 RhCMV/SIV疫苗功效预测全血转录组特征的起源和组织效应的系统分析
- 批准号:
10723639 - 财政年份:2023
- 资助金额:
-- - 项目类别:
Immunologic and Virologic Basis of RhCMV/SIV Vaccine-Induced Replication Arrest Efficacy
RhCMV/SIV 疫苗诱导复制抑制功效的免疫学和病毒学基础
- 批准号:
10619297 - 财政年份:2022
- 资助金额:
-- - 项目类别:
Project 3: Determination of the minimal MHC-E-restricted SIV epitope targeting required for RhCMV/SIV vaccine-mediated SIV replication arrest efficacy
项目 3:确定 RhCMV/SIV 疫苗介导的 SIV 复制抑制功效所需的最小 MHC-E 限制性 SIV 表位靶向
- 批准号:
10709020 - 财政年份:2022
- 资助金额:
-- - 项目类别:
Immunologic and Virologic Basis of RhCMV/SIV Vaccine-Induced Replication Arrest Efficacy
RhCMV/SIV 疫苗诱导复制抑制功效的免疫学和病毒学基础
- 批准号:
10709002 - 财政年份:2022
- 资助金额:
-- - 项目类别:
Project 3: Determination of the minimal MHC-E-restricted SIV epitope targeting required for RhCMV/SIV vaccine-mediated SIV replication arrest efficacy
项目 3:确定 RhCMV/SIV 疫苗介导的 SIV 复制抑制功效所需的最小 MHC-E 限制性 SIV 表位靶向
- 批准号:
10619304 - 财政年份:2022
- 资助金额:
-- - 项目类别:
Development of Immunogenicity- and Efficacy-Optimized CMV Vectors for an HIV/AIDS Vaccine
用于 HIV/AIDS 疫苗的免疫原性和功效优化的 CMV 载体的开发
- 批准号:
9883700 - 财政年份:2017
- 资助金额:
-- - 项目类别:
Development and In Vivo Characterization of Safety-Enhanced RhCMV/SIV Vectors
安全性增强的 RhCMV/SIV 载体的开发和体内表征
- 批准号:
8227957 - 财政年份:2011
- 资助金额:
-- - 项目类别:
ROLE OF MEMORY T CELL DYNAMICS IN SIV INFECTION
记忆 T 细胞动力学在 SIV 感染中的作用
- 批准号:
8357743 - 财政年份:2011
- 资助金额:
-- - 项目类别:
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