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DESCRIPTION (provided by applicant): Frailty is a complication of aging resulting from a dysregulation of multiple systems leading to increased morbidity, and ultimately increased mortality. The prevalence of frailty is 3-fold higher in human immunodeficiency virus type-1 (HIV-1) infected patients than age-matched HIV-negative controls, and occurs 20 years earlier than would be expected in HIV-1-negative aging patients. Preliminary analyses of ongoing studies of frailty by our group suggest a previously unrecognized association between immune activation, immune senescence, and clinical frailty in HIV-1-infected persons treated with highly-active antiretroviral therapy (HAART). The global aim of this proposal is to understand the mechanisms of immune dysfunction in HIV-1-infected frail individuals. To evaluate the global aim, we will use stored samples from HIV-1 infected frail individuals and matched HIV-1 infected non-frail controls to 1) Determine the role of chronic cytomegalovirus (CMV) co-infection in HIV-related frailty through CMV-antigen stimulation of T-cells 2) Investigate the role of microbial gut translocation in HIV-related frailty through plasma lipopolysaccharide (LPS) and soluble activation marker CD14 (sCD14) and 3) Use microarray analysis of human T-cell genes to identify potential gene expression patterns associated with the frail phenotype in HIV-1 infected persons. The proposed research will provide the first analysis of the role of chronic CMV infection, microbial translocation, and polymorphisms in T- cells in the development of HIV-1-related frailty. The results will have significant clinical implications in efforts to diagnose, treat, and prevent frailty in HIV-1-infected and uninfected individuals. PUBLIC HEALTH RELEVANCE: The proposed research will provide the first analysis of the role of chronic CMV infection, microbial translocation, and polymorphisms in T-cells in the development of HIV-related frailty. The results will have significant clinical implications in efforts to diagnose, treat, and prevent frailty in HIV-infected and uninfected individuals.
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Mentoring Across Disciplines: Aging and Infectious Diseases with a Focus on Mobility
  • 批准号:
    10757167
  • 项目类别:
  • 资助金额:
    $19.19万
  • 财政年份:
    2023
  • 负责人:
    Kristine Mace Erlandson
  • 依托单位:
Mitochondria and Muscle within the HEALTH Study
  • 批准号:
    10841249
  • 项目类别:
  • 资助金额:
    $40.31万
  • 财政年份:
    2020
  • 负责人:
    Kristine Mace Erlandson
  • 依托单位:
The High-Intensity Exercise to Attenuate Limitations and Train Habits (HEALTH) in Older Adults with HIV
  • 批准号:
    10448379
  • 项目类别:
  • 资助金额:
    $76.63万
  • 财政年份:
    2020
  • 负责人:
    Kristine Mace Erlandson
  • 依托单位:
The High-Intensity Exercise to Attenuate Limitations and Train Habits (HEALTH) in Older Adults with HIV
  • 批准号:
    9926614
  • 项目类别:
  • 资助金额:
    $79.99万
  • 财政年份:
    2020
  • 负责人:
    Kristine Mace Erlandson
  • 依托单位:
国内基金
海外基金
补阳还五汤通过AGE-RAGE通路调控脓毒症免疫失衡的机制与转化研究
靶向递送一氧化碳调控AGE-RAGE级联反应促进糖尿病创面愈合研究
  • 批准号:
    JCZRQN202500010
  • 项目类别:
    省市级项目
  • 资助金额:
    --
  • 批准年份:
    2025
  • 负责人:
  • 依托单位:
对香豆酸抑制AGE-RAGE-Ang-1通路改善海马血管生成障碍发挥抗阿尔兹海默病作用
  • 批准号:
    2025JJ70209
  • 项目类别:
    省市级项目
  • 资助金额:
    --
  • 批准年份:
    2025
  • 负责人:
    雷芬芳
  • 依托单位:
AGE-RAGE通路调控慢性胰腺炎纤维化进程的作用及分子机制
  • 批准号:
    --
  • 项目类别:
    面上项目
  • 资助金额:
    --
  • 批准年份:
    2024
  • 负责人:
    万荣
  • 依托单位: