Role of CD8+ T Cells in The Pathogenesis of HIV Disease
Role of CD8+ T Cells in The Pathogenesis of HIV Disease
批准号:
6809117
负责人:
Tae-Wook Chun
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
关键词:
CD38 molecule CD8 molecule HIV infections clinical research cytotoxic T lymphocyte flow cytometry human immunodeficiency virus human subject human tissue interferon gamma microorganism immunology statistics /biometry virus antigen virus cytopathogenic effect virus infection mechanism virus load virus replication
中文摘要
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英文摘要
CD8+ T cells are critical for effective host defenses against viral infections. Previous studies addressing human immunodeficiency virus (HIV)-induced immune responses in infected individuals have suggested that CD8+ T cells play an important role in controlling viral replication. However, despite an abundance of HIV-specific CD8+ T cells, viral replication is not contained in the majority of HIV-infected individuals in the absence of effective antiretroviral therapy. Active HIV replication is associated with numerous immunologic changes, most notable and consistent of which is an increase in CD8+ T cells expressing CD38. Previous studies have demonstrated that the expression of CD38 on CD8+ T cells is associated with poor prognostic outcome in infected individuals with detectable plasma viremia; however, the relationship between the expression of CD38 and the frequency of HIV-specific CD8+ T cells is unclear. In the present study, we demonstrate a direct correlation between the level of HIV-specific CD8+ T cells and the percentage of CD8+ T cells expressing CD38 in untreated HIV-infected individuals. HIV-specific CD8+ T cells were shown to be evenly distributed between CD38-CD8+ and CD38+CD8+ T cells in patients with a low percentage of CD8+ T cells expressing CD38 whereas their distribution was skewed toward the CD38+CD8+ T cell population in patients with a high percentage of CD8+ T cells expressing CD38. In addition, a direct correlation was observed between the frequency of HIV-specific CD8+ T cells that were found in the CD38+CD8+ T cell population and the percentage of CD8+ T cells expressing CD38. Our data suggest that a substantial proportion of the HIV-specific CD8+ T cells present in the population of CD38+CD8+ T cells in infected individuals with active viral replication arise by HIV-driven aberrant immune activation and may not manifest effective cytolytic activitiy against infected targets, thus providing an explanation why HIV is not successfully contained by CD8+ T cells in such individuals. Therefore, the large proportion of HIV-specific CD8+ T cells that express CD38 may reflect a defective virus-specific immune response in HIV-infected individuals.
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Role Of Viral Reservoirs In The Pathogenesis Of Hiv Dise
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批准号:6669763
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项目类别:
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资助金额:$0.0万
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负责人:Tae-Wook Chun
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依托单位:
Immunologic Strategies Directed Toward HIV Infection
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批准号:7592256
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项目类别:
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资助金额:$59.67万
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负责人:Tae-Wook Chun
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依托单位:
Role of Viral Reservoirs in the Pathogenesis of HIV Disease
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批准号:10249839
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项目类别:
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资助金额:$196.9万
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负责人:Tae-Wook Chun
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依托单位:
Immunologic Strategies Directed Toward HIV Infection
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批准号:7196678
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项目类别:
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资助金额:$0.0万
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财政年份:--
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负责人:Tae-Wook Chun
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Role Of Viral Reservoirs In The Pathogenesis Of HIV Dise
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批准号:7303834
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资助金额:$0.0万
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负责人:Tae-Wook Chun
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Role of Viral Reservoirs in the Pathogenesis of HIV Disease
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批准号:10915932
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资助金额:$297.95万
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负责人:Tae-Wook Chun
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Effect of IL-2 on the pool of latently infected, resting CD4+ T cells in HIV-1
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批准号:6227852
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资助金额:$0.0万
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财政年份:--
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负责人:Tae-Wook Chun
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依托单位:
Immunologic Strategies Directed Toward HIV Infection
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批准号:7303858
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资助金额:$0.0万
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财政年份:--
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负责人:Tae-Wook Chun
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Role of HIV Reservoirs in the Pathogenesis of HIV Disease
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批准号:6431717
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项目类别:
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资助金额:$0.0万
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财政年份:--
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负责人:Tae-Wook Chun
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依托单位:
Role Of Viral Reservoirs In Pathogenesis Of HIV Disease
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批准号:7196655
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项目类别:
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资助金额:$0.0万
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财政年份:--
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负责人:Tae-Wook Chun
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依托单位:
Immunologic and Virologic Strategies Directed Toward HIV
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批准号:6986987
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项目类别:
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资助金额:$0.0万
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财政年份:--
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负责人:Tae-Wook Chun
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依托单位:
Role of Viral Reservoirs in the Pathogenesis of HIV Disease
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批准号:10689597
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项目类别:
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资助金额:$201.71万
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财政年份:--
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负责人:Tae-Wook Chun
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依托单位:
海外基金