SPECIFICITY, DISTRIBUTION AND FUNCTION OF GD T CELLS

GD T 细胞的特异性、分布和功能

基本信息

  • 批准号:
    6137151
  • 负责人:
  • 金额:
    $ 32.23万
  • 依托单位:
  • 依托单位国家:
    美国
  • 项目类别:
  • 财政年份:
    1989
  • 资助国家:
    美国
  • 起止时间:
    1989-04-01 至 2001-12-31
  • 项目状态:
    已结题

项目摘要

DESCRIPTION (Adapted from the Investigator's abstract): So far as is known, all vertebrates contain two types of T-cells, an alpha/beta and a gamma/delta T-cell, distinguished by their alpha/beta and gamma/delta T-cell antigen receptors. The role of alpha/beta T-cells is reasonably well understood, but this is not the case for gamma/delta T-cells. Studies from many groups suggest that gamma/delta T-cells are quite different from alpha/beta T-cells in terms of antigen recognition and anatomical localization. But, there has been a longstanding need for a bioassay, by which to assess the function of gamma/delta T-cells and the effector mechanisms(s) that underlie it. In part, the problem has been the scarcity of gamma/delta T-cells, that in mice and humans are much less abundant than alpha/beta T-cells. To tackle these issues, the investigators' laboratory has developed mice that lack alpha/beta T-cells, and have challenged those, together with mice that lack gamma/delta T-cells with a natural protozoan parasite that targets the intestinal epithelium, a resident site of gamma/delta T-cells. The investigators found that the normal response of mice to this parasite is significantly affected by the deletion of either alpha/beta T-cells or gamma/delta T-cells, but in different ways. Whereas alpha/beta T-cells are essential for protection of the host, gamma/delta T-cell deficiency is associated with severe pathology. Thus the investigators believe that alpha/beta and gamma/delta T-cells indeed represent very different components of the immune system, and that an understanding of gamma/delta T-cell functions is therefore essential for our understanding of immune-related pathologies, particularly of the gut, e.g., inflammatory bowel disease. The bioassay for gamma/delta T-cells provided by the investigators' system should facilitate such an improved understanding. Both cellular and genetic approaches will be adopted. The investigators shall undertake the analysis of another bioassay for gamma/delta T-cells, for which the investigators have recently developed convincing evidence. In this assay, gamma/delta T-cells offer a significant level of anti-microbial protection without establishing immunity. Together the study of these assays may reveal why gamma/delta T-cells are so highly conserved.
描述(改编自研究者摘要):就目前所知,

项目成果

期刊论文数量(12)
专著数量(0)
科研奖励数量(0)
会议论文数量(0)
专利数量(0)
T cell receptor-alpha beta-deficient mice fail to develop colitis in the absence of a microbial environment.
  • DOI:
  • 发表时间:
    1997
  • 期刊:
  • 影响因子:
    0
  • 作者:
    L. Dianda;A. Hanby;N. Wright;A. Sebestény;A. Hayday;M. Owen
  • 通讯作者:
    L. Dianda;A. Hanby;N. Wright;A. Sebestény;A. Hayday;M. Owen
Pathogenesis of autoimmunity in alphabeta T cell-deficient lupus-prone mice.
Alphata T 细胞缺陷型狼疮易感小鼠自身免疫的发病机制。
  • DOI:
    10.1046/j.1365-2249.1998.00424.x
  • 发表时间:
    1998
  • 期刊:
  • 影响因子:
    4.6
  • 作者:
    Peng,SL;Cappadona,J;McNiff,JM;Madaio,MP;Owen,MJ;Hayday,AC;Craft,J
  • 通讯作者:
    Craft,J
Gamma delta T-cell lines isolated from intestinal epithelium respond to a B-cell lymphoma.
从肠上皮分离的 γ δ T 细胞系对 B 细胞淋巴瘤有反应。
  • DOI:
  • 发表时间:
    1993
  • 期刊:
  • 影响因子:
    6.4
  • 作者:
    Sano,Y;Dudley,E;Carding,S;Lin,RH;Hayday,AC;JanewayJr,CA
  • 通讯作者:
    JanewayJr,CA
Propagation and regulation of systemic autoimmunity by gammadelta T cells.
  • DOI:
    10.4049/jimmunol.157.12.5689
  • 发表时间:
    1996-12
  • 期刊:
  • 影响因子:
    4.4
  • 作者:
    S. Peng;M. Madaio;A. Hayday;J. Craft
  • 通讯作者:
    S. Peng;M. Madaio;A. Hayday;J. Craft
An alphabeta T-cell-independent immunoprotective response towards gut coccidia is supported by gammadelta cells.
针对肠道球虫的非 Alphata T 细胞独立的免疫保护反应得到了 γδ 细胞的支持。
  • DOI:
    10.1046/j.1365-2567.2000.00122.x
  • 发表时间:
    2000
  • 期刊:
  • 影响因子:
    6.4
  • 作者:
    Smith,AL;Hayday,AC
  • 通讯作者:
    Hayday,AC
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ROBERT E. TIGELAAR其他文献

ROBERT E. TIGELAAR的其他文献

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{{ truncateString('ROBERT E. TIGELAAR', 18)}}的其他基金

Genome Wide Analysis of Melanocytic Lesions
黑素细胞病变的全基因组分析
  • 批准号:
    7508860
  • 财政年份:
    2007
  • 资助金额:
    $ 32.23万
  • 项目类别:
Administrative Core
行政核心
  • 批准号:
    7508857
  • 财政年份:
    2007
  • 资助金额:
    $ 32.23万
  • 项目类别:
Career Development Award Program
职业发展奖励计划
  • 批准号:
    8915626
  • 财政年份:
    2006
  • 资助金额:
    $ 32.23万
  • 项目类别:
CAREER DEVELOPMENT PROGRAM
职业发展计划
  • 批准号:
    7147307
  • 财政年份:
    2006
  • 资助金额:
    $ 32.23万
  • 项目类别:
Career Development Award Program
职业发展奖励计划
  • 批准号:
    8719050
  • 财政年份:
    2006
  • 资助金额:
    $ 32.23万
  • 项目类别:
DEVELOPMENTAL RESEARCH PROGRAM
发展研究计划
  • 批准号:
    7147306
  • 财政年份:
    2006
  • 资助金额:
    $ 32.23万
  • 项目类别:
Career Development Award Program
职业发展奖励计划
  • 批准号:
    8389784
  • 财政年份:
    2006
  • 资助金额:
    $ 32.23万
  • 项目类别:
Developmental Research Program
发展研究计划
  • 批准号:
    8389783
  • 财政年份:
    2006
  • 资助金额:
    $ 32.23万
  • 项目类别:
Developmental Research Program
发展研究计划
  • 批准号:
    8557724
  • 财政年份:
    2006
  • 资助金额:
    $ 32.23万
  • 项目类别:
Developmental Research Program
发展研究计划
  • 批准号:
    8719049
  • 财政年份:
    2006
  • 资助金额:
    $ 32.23万
  • 项目类别:

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