Dendritic cells in psoriasis and effects of efalizumab

银屑病中的树突状细胞和依法珠单抗的作用

基本信息

  • 批准号:
    7588741
  • 负责人:
  • 金额:
    $ 13.54万
  • 依托单位:
  • 依托单位国家:
    美国
  • 项目类别:
  • 财政年份:
    2006
  • 资助国家:
    美国
  • 起止时间:
    2006-04-01 至 2011-03-31
  • 项目状态:
    已结题

项目摘要

CANDIDATE: I am a dermatologist (MD PhD) and my broad career goal is to be an independent physician- scientist in human translational skin research, particularly in the area of psoriasis. I am proposing to become a multi-disciplinary patient-oriented researcher, with an excellent grasp of a number of technologies, which will allow me to investigate therapeutic, mechanistic and pathologic questions appropriately and deeply. ENVIRONMENT: Rockefeller University is a world-renowned institution with a rich history of bench-bedside research. It provides an ideal environment to carry out this type of clinical research with a dedicated GCRC- funded research hospital, outstanding laboratories, excellent core facilities and equipment, an innovative Clinical Scholars Program for translational research trainees, and several inspiring lecture and seminar programs. There is no fee-for-service medicine at Rockefeller University, so I can dedicate 100% of my time to this career development plan. RESEARCH PROJECT: Psoriasis offers an excellent model of type 1 autoimmunity, and there there is no ideal animal model of psoriasis to study. In the context of a clinical trial with efalizumab (anti-CD11a) for psoriasis, we identified a new type of cutaneous dendritic cell (DC) (CD11c+, HLA-DR+, CD86+, CD40+), which constitutes the most abundant type of leukocyte in psoriasis lesions. It also expresses TNF and iNOS, so these cells may be the human equivalent of recently described murine TNF- and indicible nitric oxide synthase (iNOS)-producing (TIP)-DCs. I plan to begin basic characterization of complex DC subsets that exist in blood and skin of humans, using efalizumab as a tool to modulate psoriasis disease activity, so that the contribution of different DC subsets to disease pathogenesis can be better refined. Furthermore, I will determine the extent to which efalizumab has direct effects on growth, differentiation and activation of DCs versus indirect effects through T cell modulation.
我是一名皮肤科医生(医学博士),我的职业目标是成为一名独立的医生

项目成果

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MICHELLE A LOWES其他文献

MICHELLE A LOWES的其他文献

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{{ truncateString('MICHELLE A LOWES', 18)}}的其他基金

Origin and Function of Inflammatory Dendritic Cells in Psoriasis.
银屑病炎症树突状细胞的起源和功能。
  • 批准号:
    8510576
  • 财政年份:
    2011
  • 资助金额:
    $ 13.54万
  • 项目类别:
Origin and Function of Inflammatory Dendritic Cells in Psoriasis.
银屑病炎症树突状细胞的起源和功能。
  • 批准号:
    8332734
  • 财政年份:
    2011
  • 资助金额:
    $ 13.54万
  • 项目类别:
Origin and Function of Inflammatory Dendritic Cells in Psoriasis.
银屑病炎症树突状细胞的起源和功能。
  • 批准号:
    8116236
  • 财政年份:
    2011
  • 资助金额:
    $ 13.54万
  • 项目类别:
Dendritic cells in psoriasis and effects of efalizumab
银屑病中的树突状细胞和依法珠单抗的作用
  • 批准号:
    7924415
  • 财政年份:
    2009
  • 资助金额:
    $ 13.54万
  • 项目类别:
Dendritic cells in psoriasis and effects of efalizumab
银屑病中的树突状细胞和依法珠单抗的作用
  • 批准号:
    7392308
  • 财政年份:
    2006
  • 资助金额:
    $ 13.54万
  • 项目类别:
Dendritic cells in psoriasis and effects of efalizumab
牛皮癣中的树突状细胞和依法珠单抗的作用
  • 批准号:
    7789527
  • 财政年份:
    2006
  • 资助金额:
    $ 13.54万
  • 项目类别:
Dendritic cells in psoriasis and effects of efalizumab
牛皮癣中的树突状细胞和依法珠单抗的作用
  • 批准号:
    7034155
  • 财政年份:
    2006
  • 资助金额:
    $ 13.54万
  • 项目类别:

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