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FUNCTIONAL & PHENOTYPIC ANALYSIS OF T-CELLS IN FIV-FAIDS

FUNCTIONAL & PHENOTYPIC ANALYSIS OF T-CELLS IN FIV-FAIDS
功能性
批准号:
3177632
负责人:
Janet K. Yamamoto
金额:
$19.75万
依托单位国家:
美国
项目类别:
财政年份:
1989
资助国家:
美国
项目状态:
已结题
起止时间:
1989-07-15 至 1992-06-30

项目摘要

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中文摘要
翻译
一种类似于人类免疫缺陷病毒(HIV)的猫慢病毒 在我们的实验室中与患有免疫缺陷的家猫隔离 综合症,并被命名为猫免疫缺陷病毒(FIV)。标志 猫感染 FIV 的主要原因是受感染者的易感性增加 动物继发感染的情况与观察到的情况非常相似 用于人类艾滋病毒感染。另外,还有实验结果 表明受感染猫的 T 细胞免疫存在缺陷。使用 感染FIV的猫作为人类艾滋病的小动物模型应该 因此被考虑,因为它更经济、更快速, 与猫白血病病毒模型更接近的人类艾滋病模型 或通过除灵长类动物模型外的其他动物慢病毒。 本项目的目的是利用AID的FIV模型来评估 T 淋巴细胞在 FIV-FAIDS 免疫发病机制中的作用。在这个 评估猫 T 所需的研究、猫试剂和功能测定 淋巴细胞网络将得到发展。这些试剂和程序将 然后用于监测 FIV 各个阶段的 T 细胞功能 猫的感染。本研究还将尝试解决以下问题 目前尚不清楚的 FIV 感染要点: (1) 感染者的身份 被 FIV 感染的 T 细胞亚群以及 T 细胞的作用 抗原呈递细胞。 (2) 如果确实存在 T 细胞亚群缺陷 那么这些缺陷在 FIV-免疫发病中的作用 艾滋病。该项目的总体意义是确定 艾滋病在动物中发生并产生免疫学的机制 可用于预防艾滋病病毒感染的方法。的 这些研究的结果应该有助于确定预防措施和 有助于对抗人类艾滋病毒感染的治疗策略。
英文摘要
A feline lentivirus resembling human immunodeificency virus (HIV) was siolated in our laboratory from domestic cats with immunodeficiency syndrome and was named feline immunodeiciency virus (FIV). The hallmark of FIV infection in cats is the increased susceptibility of the infected animals to secondary infections much similar to what has been observed for HIV infection of humans. In addition, there are experimental results suggesting a defect in T cell immunity in the infected cats. The use of FIV infection of cats as a small animal model for human AIDS should therefore be considered because it is far more economical, more rapid, and much closer model for human AIDS that those of feline leukemia virus or by other animal lentiviruses with the exception of the primate models. The purpose of this project is to use the FIV model of AIDs to evaluate the role of T lymphocytes in the immunopathogenesis of FIV-FAIDS. In this study, feline reagents and functional assays needed to evaluate feline T lymphocyte network will be developed. These reagents and procedures will then be used to monitor the T-cell functions during various stages of FIV infection in cats. This study will also attempt to address the following points of FIV infection which is still unknown: (1) The identity of the T-cell subset(s) that is/are infected by FIV and the role of T cells as antigen presenting cells. (2) If subsets of T-cells deficiencies do exist then the role of these deficiencies in the immunopathogensis of FIV- FAIDS. The overall significance of this project is to identify the mechanism(s) by which AIDS occurs in animals and to develop immunological approaches that could be used to prevent AIDS virus infection. The results from these studies should help identify prophylaptic and therapeutic strategies that will help combat HIV infection of humans.
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Protective CMI mechanisms of a dual-subtype FIV vaccine
  • 批准号:
    7575838
  • 项目类别:
  • 资助金额:
    $9.87万
  • 财政年份:
    2008
  • 负责人:
    Janet K. Yamamoto
  • 依托单位:
HIV/FIV-cat model: a model to identify vaccine epitopes
  • 批准号:
    7253137
  • 项目类别:
  • 资助金额:
    $35.73万
  • 财政年份:
    2006
  • 负责人:
    Janet K. Yamamoto
  • 依托单位:
HIV/FIV-cat model: a model to identify vaccine epitopes
  • 批准号:
    7469353
  • 项目类别:
  • 资助金额:
    $35.08万
  • 财政年份:
    2006
  • 负责人:
    Janet K. Yamamoto
  • 依托单位:
HIV/FIV-cat model: a model to identify vaccine epitopes
  • 批准号:
    7166729
  • 项目类别:
  • 资助金额:
    $37.91万
  • 财政年份:
    2006
  • 负责人:
    Janet K. Yamamoto
  • 依托单位:
海外基金