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Role of Exogenous Activation of the Immune System in the Pathogenesis of HIV dis

Role of Exogenous Activation of the Immune System in the Pathogenesis of HIV dis
免疫系统的外源激活在 HIV 发病机制中的作用
批准号:
6099018
负责人:
Mario Ostrowski
金额:
$0.0万
依托单位国家:
美国
项目类别:
财政年份:
--
资助国家:
美国
项目状态:
未结题
起止时间:
至

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中文摘要
翻译
这个项目的目的是描述病原
英文摘要
This project is directed at delineating the pathogenic mechanisms of HIV infection and the role of immune activation in the propagation of disease and destruction of the immune system. We have demonstrated that, after tetanus toxoid booster inoculation, HIV-1 infected patients had transient increases in plasma viremia after immunization, increases in proviral burden, and increased viral load within lymph nodes. HIV was more easily isolated from PBMCs from the majority of patients after immunization than before immunization. We also demonstrated an enhanced susceptibility of normal PBMCs to HIV infection in vitro after tetanus immunization. Tetanus immunization was associated with dramatic and generally reversible shifts in the composition of plasma viral quasi-species. The plasma viral bursts in most cases reflected a non-specific increase in viral replication, secondary to an expanded pool of susceptible CD4+ T cells. In one patient, however, immunization favored the expansion of M-tropic(NSI) over dual tropic(SI) viruses. In one of three patients the data suggested that immune activation resulted in the appearance in plasma of virus induced from latently infected cells. These findings demonstrate how antigenic stimulation influences the dynamics of HIV replication including the relative expression of different viral variants.
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会议论文
Harnessing the PIWI piRNA pathway to silence HIV
  • 批准号:
    9762886
  • 项目类别:
  • 资助金额:
    $44.1万
  • 财政年份:
    2017
  • 负责人:
    Mario Ostrowski
  • 依托单位:
The Role of CD4 T cell Help and CD40 Ligand in anti-HIV-1 Cytotoxic CD8 T cell
ROLE OF EXOGENOUS ACTIVATION OF THE IMMUNE SYSTEM IN THE PATHOGENESIS OF HIV DIS
Role of CD4 T cell Help and CD40 Ligand in anti-HIV-1 Cytotoxic T cell Responses
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