课题基金 / 基金详情

Immunogenetics of Macaques Used for Biodefense and AIDS Research

Immunogenetics of Macaques Used for Biodefense and AIDS Research
用于生物防御和艾滋病研究的猕猴免疫遗传学
批准号:
8013585
负责人:
David H. O'Connor
金额:
$55.45万
依托单位国家:
美国
项目类别:
财政年份:
2005
资助国家:
美国
项目状态:
已结题
起止时间:
2005-09-26 至 2014-06-30

项目摘要

项目成果

David H. O'Connor的其他基金

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中文摘要
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英文摘要
DESCRIPTION (provided by applicant): Macaque monkeys are the most important animal model for AIDS vaccine development and are increasingly being used in biodefense research. An individual's immunogenetics can profoundly influence susceptibility to AIDS viruses and other pathogens. Indian-origin rhesus macaques have the most thoroughly characterized immunogenetics; however, their availability for research is extremely limited. Chinese-origin rhesus macaques, cynomolgus macaques, and pig-tailed macaques are increasingly relied upon to alleviate the shortage of Indian- rhesus macaques. As studies with these macaques become more common, there is a newfound appreciation that they may offer compelling advantages over Indian-origin rhesus macaques for specific studies. To study cellular immunity to AIDS viruses and biodefense, a comprehensive understanding of major histocompatibility complex (MHC) and killer immunoglobulin receptor (KIR) genetics is required. In the initial project period of this grant, MHC class I and II alleles were sequenced from cynomolgus macaques from different origins and the first MHC peptide binding motifs in cynomolgus macaques were determined. In this renewal, we will continue and expand this project by completing: Specific Aim 1, in which commonly expressed MHC class I and II alleles will be sequenced from cynomolgus, Chinese rhesus, and pig-tailed macaques. Specific Aim 2, in which full length KIR alleles will be sequenced from the same populations of macaques. Specific Aim 3, in which 8 MHC class I and 8 MHC class II peptide binding motifs will be determined. These Aims will take advantage of recent developments in high-throughput 'next generation' DNA sequencing to rapidly characterize full-length MHC and KIR alleles. At least 300 heretofore novel MHC class 1,150 MHC class II, and 300 KIR sequences will be identified. The experience of the investigative team in macaque immunogenetics, deep sequencing, and MHC biochemistry uniquely qualifies them to continue this important research. PUBLIC HEALTH RELEVANCE (provided by applicant): Macaque monkeys are widely used in the development and testing of prophylactic vaccines against AIDS viruses and pathogens with biodefense potential. Major histocompatibility complex (MHC) and killer immunoglobuline receptor (KIR) genetics influence susceptibility to these diseases. We will sequence novel alleles and define their functional attributes in macaque populations used for infectious disease research.
期刊论文(2)
专著(0)
科研奖励(0)
会议论文
DOI: 10.1007/s00251-013-0744-3
发表时间: 2014-01
期刊: IMMUNOGENETICS
影响因子: 3.2
作者: [Dudley, Dawn M., Karl, Julie A., Creager, Hannah M., Bohn, Patrick S., Wiseman, Roger W., O'Connor, David H.]
通讯作者: O'Connor, David H.
DOI: 10.3389/fimmu.2011.00075
发表时间: 2011
期刊: Frontiers in immunology
影响因子: 7.3
作者: [Keskin DB, Reinhold B, Lee SY, Zhang G, Lank S, O'Connor DH, Berkowitz RS, Brusic V, Kim SJ, Reinherz EL]
通讯作者: Reinherz EL
Anticipating and rapidly responding to respiratory virus outbreaks with continuous air sampling in K-12 schools
  • 批准号:
    10658581
  • 项目类别:
  • 资助金额:
    $78.87万
  • 财政年份:
    2023
  • 负责人:
    David H. O'Connor
  • 依托单位:
Zika virus pathophysiology during pregnancy
  • 批准号:
    10468066
  • 项目类别:
  • 资助金额:
    $202.05万
  • 财政年份:
    2018
  • 负责人:
    David H. O'Connor
  • 依托单位:
Core-002
  • 批准号:
    10667759
  • 项目类别:
  • 资助金额:
    $33.12万
  • 财政年份:
    2018
  • 负责人:
    David H. O'Connor
  • 依托单位:
Zika virus pathophysiology during pregnancy
  • 批准号:
    9752458
  • 项目类别:
  • 资助金额:
    $203.08万
  • 财政年份:
    2018
  • 负责人:
    David H. O'Connor
  • 依托单位: