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英文摘要
Although anal intercourse is a common mode of HIV-1 transmission, particularly for men who have sex with men, many fundamental and mechanistic questions remain. The long-term objective of this study is to understand the early events in HIV-1 rectal transmission and to gain new insights, which will potentially lead to new intervention strategies, including vaccines and topical microbicides optimized for rectal use. Studying HIV-1 vaginal transmission in the highly relevant SIV-rhesus macaque model has revealed important events critical for transmission, such as target cell availability, innate immune response, and inflammation at the portal of entry, all factors which play a key role in transmission. Because the anatomical/histological features and the physiological functions of vagina and cervix differ from the rectum, we hypothesize that the underlying mechanisms and timing of HIV-1 rectal transmission will significantly differ from those of vaginal-cervical transmission. Utilizing innovative approaches and an established conceptual framework from studies of vaginal transmission, we will test this hypothesis by investigating three specific aims: 1) determine the timing, location, spatial distribution and cell types of virus-infected cells at the portal of entry and in draining and distal lymphatic tissues; 2) determine relationships between virus and susceptible target cells (CD4+ T cells, macrophages, and dendritic cells) and between virus-infected cells and the mucosal innate immune response in the rectum shortly after intra-rectal SIV inoculation, thereby determining whether changes in target-cell availability play a critical role in local expansion and systemic spread of infection; and 3) determine the spatial relationships and ratio of virus-specific CD8+ T effector cells (E) and virus-infected-target cells (T) at the portal of entry and in other tissue compartments to extent of control of virus replication, using a novel procedure combining in-situ tetramers and in-situ hybridization The proposed research is significant as it is expected to reveal important mechanisms underlying rectal transmission and potentially provide guidance for designing anti-HIV-1 vaccines and topical microbicides.
期刊论文(4)
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会议论文
DOI: 10.1038/s41426-018-0062-9
发表时间: 2018-04-04
期刊: Emerging microbes & infections
影响因子: 13.2
作者: [Yuan Z, Kang G, Daharsh L, Fan W, Li Q]
通讯作者: Li Q
Characterization of founder viruses in very early SIV rectal transmission.
在非常早期的SIV直肠传播中的创始人病毒的表征。
DOI: 10.1016/j.virol.2016.12.018
发表时间: 2017-02
期刊: Virology
影响因子: 3.7
作者: [Yuan Z, Ma F, Demers AJ, Wang D, Xu J, Lewis MG, Li Q]
通讯作者: Li Q
DOI: 10.4049/jimmunol.1502137
发表时间: 2016-02-15
期刊: Journal of immunology (Baltimore, Md. : 1950)
影响因子: --
作者: [Vargas-Inchaustegui DA, Demers A, Shaw JM, Kang G, Ball D, Tuero I, Musich T, Mohanram V, Demberg T, Karpova TS, Li Q, Robert-Guroff M]
通讯作者: Robert-Guroff M
Mechanisms of resistance to immune therapy in NSCLC
  • 批准号:
    10093111
  • 项目类别:
  • 资助金额:
    $27.12万
  • 财政年份:
    2020
  • 负责人:
    Qingsheng Li
  • 依托单位:
Mechanisms of resistance to immune therapy in NSCLC
  • 批准号:
    10577776
  • 项目类别:
  • 资助金额:
    $25.11万
  • 财政年份:
    2020
  • 负责人:
    Qingsheng Li
  • 依托单位:
Mechanisms of resistance to immune therapy in NSCLC
  • 批准号:
    10333209
  • 项目类别:
  • 资助金额:
    $26.99万
  • 财政年份:
    2020
  • 负责人:
    Qingsheng Li
  • 依托单位:
Next Generation Broadly Neutralizing Antibodies to Clear HIV-1 Reservoir
  • 批准号:
    10515649
  • 项目类别:
  • 资助金额:
    $77.84万
  • 财政年份:
    2018
  • 负责人:
    Qingsheng Li
  • 依托单位:
海外基金