SPECIFICITY, DISTRIBUTION AND FUNCTION OF GD T CELLS
SPECIFICITY, DISTRIBUTION AND FUNCTION OF GD T CELLS
批准号:
6137151
负责人:
ROBERT E. TIGELAAR
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
项目状态:
已结题
起止时间:
1989-04-01 至 2001-12-31
中文摘要
点击翻译按钮获取中文摘要
英文摘要
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.
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DOI:
--
发表时间:
1997
期刊:
The American journal of pathology
影响因子:
--
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:
Clinical and experimental immunology
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:
Immunology
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
DOI:
10.4049/jimmunol.157.12.5689
发表时间:
1996-12
期刊:
Journal of immunology
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:
Immunology
影响因子:
6.4
作者:
[Smith,AL, Hayday,AC]
通讯作者:
Hayday,AC
共 8 条
Genome Wide Analysis of Melanocytic Lesions
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批准号:7508860
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项目类别:
-
资助金额:$3.97万
-
财政年份:2007
-
负责人:ROBERT E. TIGELAAR
-
依托单位:
Administrative Core
-
批准号:7508857
-
项目类别:
-
资助金额:$10.88万
-
财政年份:2007
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负责人:ROBERT E. TIGELAAR
-
依托单位:
Career Development Award Program
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批准号:8915626
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项目类别:
-
资助金额:$6.25万
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财政年份:2006
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负责人:ROBERT E. TIGELAAR
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依托单位:
CAREER DEVELOPMENT PROGRAM
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批准号:7147307
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项目类别:
-
资助金额:$6.54万
-
财政年份:2006
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负责人:ROBERT E. TIGELAAR
-
依托单位:
Career Development Award Program
-
批准号:8719050
-
项目类别:
-
资助金额:$6.15万
-
财政年份:2006
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负责人:ROBERT E. TIGELAAR
-
依托单位:
DEVELOPMENTAL RESEARCH PROGRAM
-
批准号:7147306
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项目类别:
-
资助金额:$14.37万
-
财政年份:2006
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负责人:ROBERT E. TIGELAAR
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依托单位:
Career Development Award Program
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批准号:8389784
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项目类别:
-
资助金额:$6.56万
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财政年份:2006
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负责人:ROBERT E. TIGELAAR
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依托单位:
Developmental Research Program
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批准号:8389783
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项目类别:
-
资助金额:$9.37万
-
财政年份:2006
-
负责人:ROBERT E. TIGELAAR
-
依托单位:
Developmental Research Program
-
批准号:8557724
-
项目类别:
-
资助金额:$9.6万
-
财政年份:2006
-
负责人:ROBERT E. TIGELAAR
-
依托单位:
Developmental Research Program
-
批准号:8719049
-
项目类别:
-
资助金额:$8.79万
-
财政年份:2006
-
负责人:ROBERT E. TIGELAAR
-
依托单位:
Developmental Research Program
-
批准号:9126437
-
项目类别:
-
资助金额:$8.84万
-
财政年份:2006
-
负责人:ROBERT E. TIGELAAR
-
依托单位:
Career Development Award Program
-
批准号:8557725
-
项目类别:
-
资助金额:$6.72万
-
财政年份:2006
-
负责人:ROBERT E. TIGELAAR
-
依托单位:
Core A - Administration (Robert Tigelaar, PI)
-
批准号:6756346
-
项目类别:
-
资助金额:$13.07万
-
财政年份:2004
-
负责人:ROBERT E. TIGELAAR
-
依托单位:
Regulation of Cutaneous Inflammation by local gd T Cells
-
批准号:6906535
-
项目类别:
-
资助金额:$36.59万
-
财政年份:2003
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负责人:ROBERT E. TIGELAAR
-
依托单位:
Regulation of Cutaneous Inflammation by local gd T Cells
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批准号:6796239
-
项目类别:
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资助金额:$36.59万
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财政年份:2003
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负责人:ROBERT E. TIGELAAR
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依托单位:
Regulation of Cutaneous Inflammation by local gd T Cells
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批准号:7106514
-
项目类别:
-
资助金额:$32.88万
-
财政年份:2003
-
负责人:ROBERT E. TIGELAAR
-
依托单位:
Regulation of Cutaneous Inflammation by local gd T Cells
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批准号:6681745
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项目类别:
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资助金额:$38.08万
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财政年份:2003
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负责人:ROBERT E. TIGELAAR
-
依托单位:
Regulation of Cutaneous Inflammation by local gd T Cells
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批准号:7272780
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项目类别:
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资助金额:$31.92万
-
财政年份:2003
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负责人:ROBERT E. TIGELAAR
-
依托单位:
ALPHA BETA T CELL INDEPENDENT B CELL FUNCTION
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批准号:2076048
-
项目类别:
-
资助金额:$22.62万
-
财政年份:1996
-
负责人:ROBERT E. TIGELAAR
-
依托单位:
ALPHA BETA T CELL INDEPENDENT B CELL FUNCTION
-
批准号:2599415
-
项目类别:
-
资助金额:$0.18万
-
财政年份:1996
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负责人:ROBERT E. TIGELAAR
-
依托单位:
海外基金