ETHANOL AND CD4 CELL DEPENDENT IMMUNITY
ETHANOL AND CD4 CELL DEPENDENT IMMUNITY
批准号:
2384348
负责人:
DAVID ABRAHAM
金额:
$11.34万
依托单位国家:
美国
项目类别:
财政年份:
1997
资助国家:
美国
项目状态:
已结题
起止时间:
1997-07-01 至 1999-06-30
关键词:
B lymphocyte Leishmania major Nematoda SCID mouse alcoholic beverage consumption cellular immunity cytokine disease /disorder model dogs dosage enzyme linked immunosorbent assay eosinophil ethanol helper T lymphocyte humoral immunity immunization laboratory mouse macrophage parasitic diseases protozoal infection tissue /cell culture
中文摘要
人类和实验动物的乙醇消耗量
被证明会抑制许多特定的免疫功能。它有
有人假设,免疫反应受到抑制,
导致传染病流行率上升,
酗酒者的肿瘤研究表明,慢性乙醇
消耗抑制T淋巴细胞辅助功能。CD4 T-
辅助细胞可分为两个不同的表型亚群
通过不同的淋巴因子分泌模式起作用。th 1细胞
产生细胞介导的免疫; Th 2负责
抗体介导免疫小鼠寄生虫感染提供了
这是完全由以下两种方法控制的感染的主要例子:
Th 1或Th 2系统。其中两个模型已经被
彻底调查,(a)利什曼原虫,原生动物
感染,其中免疫完全依赖于Thl,
(B)粪类圆线虫,一种线虫感染,其中
免疫完全依赖于Th 2。乙醇的作用
消费对保护性免疫力的发展,这些
将确定感染,从而阐明
乙醇对Th 1和Th 2功能的影响。本研究的目的是
(i)确定给药的适当方案
用于证明对CD 4细胞的影响
功能(ii)确定乙醇对保护性
依赖于Th 1或Th 2细胞的免疫应答,和(iii)
研究乙醇引起改变的机制,
保护性免疫反应用这些获得的结果
两个寄生虫感染模型将提供有关
乙醇消耗对保护性免疫依赖性的影响
CD 4细胞。
英文摘要
Ethanol consumption in humans and in experimental animals has
been shown to depress many specific immune functions. It has
been hypothesized that the depressed immune response may
contribute to the increased prevalence of infectious diseases and
tumors in alcoholics. Studies suggest that chronic ethanol
consumption depresses T-lymphocyte helper function. CD4 T-
helper cells can be divided into two distinct phenotypic subsets
acting through different lymphokine secretion patterns. Th1 cells
give rise to cell-mediated immunity; Th2 are responsible for
antibody-mediated immunity. Parasitic infections in mice provide
the premier examples of infections controlled exclusively by either
the Thl or the Th2 system. Two of these models have been
thoroughly investigated, (a) Leishmania major, a protozoan
infection, where immunity is totally Thl dependent and
(b)Strongyloides stercoralis, a nematode infection, where
immunity is totally Th2 dependent. The effect of ethanol
consumption on the development of protective immunity to these
infections will be determined, thereby elucidating the effect of
ethanol on Thl and Th2 function. The objectives of this study are
to (i) to determine the appropriate protocol for the administration
of ethanol to mice for the demonstration of an effect on CD4 cell
function (ii) to determine the effect of ethanol on protective
immune responses dependent on either Thl or Th2 cells and (iii) to
investigate the mechanism by which ethanol causes an alteration in
the protective immune response. The results obtained with these
two parasitic infection models will provide information on the
effects of ethanol consumption on protective immunity dependent
on CD4 cells.
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会议论文
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依托单位:
ETHANOL AND CD4 CELL DEPENDENT IMMUNITY
-
批准号:2732466
-
项目类别:
-
资助金额:$11.34万
-
财政年份:1997
-
负责人:DAVID ABRAHAM
-
依托单位:
海外基金