Functional Genomic Analysis of NK and NKT Cell Immune Control of Autoimmunity
Functional Genomic Analysis of NK and NKT Cell Immune Control of Autoimmunity
批准号:
nhmrc : 137811
负责人:
Prof Alan Baxter
金额:
$46.15万
依托单位:
依托单位国家:
澳大利亚
项目类别:
NHMRC Project Grants
财政年份:
2001
资助国家:
澳大利亚
项目状态:
已结题
起止时间:
2001-01-01 至 2005-12-31
中文摘要
白色血细胞的主要群体是B细胞和T细胞,前者负责产生针对细菌等微生物的抗体,后者负责杀死病毒感染的细胞并帮助B细胞产生抗体。T和B细胞偶尔会攻击人体自身组织,导致自身免疫性疾病。这些疾病包括1型糖尿病、狼疮和贫血,并且共同代表人类发病和死亡的第三常见原因。发生自身免疫的主要原因被认为是由于负责控制这种不需要的反应的机制的失败。另外两种白色血细胞参与了这种调节,称为NK细胞和NKT细胞,每种细胞都释放重要的细胞激素。目前的项目旨在测试NK和NKT细胞的缺陷是否会导致自身免疫性疾病。为此,将使用特殊品系的小鼠(NOD小鼠)。选择他们的原因是:1)他们对一系列自身免疫性疾病(包括糖尿病,狼疮和贫血)非常敏感,2)我们和其他人发现他们缺乏NK和NKT细胞。拟议的实验分为两组,一组旨在确定这些细胞中缺陷的性质,另一组旨在确定导致这些缺陷的基因。通过这种方式,它应该有可能阐明一般自身免疫性疾病的遗传基础。所使用的方法涉及复杂的遗传分析技术,这需要产生特殊的同类系小鼠。这些小鼠类似于NOD小鼠,但除了NOD基因外,还携带来自非自身免疫品系的遗传区域,具有纠正NK和NKT细胞缺陷的潜力。通过这种方式,应该有可能确定与自身免疫性有关的疾病易感基因,并确定它们如何影响NK和NKT细胞。
英文摘要
The major populations of white blood cells responsible for learned immunity to are the B cells, which make antibody against microorganisms like bacteria, and the T cells, which kill virally infected cells and help B cells produce antibody. The T and B cells occasionally attack the body s own tissues, resulting in autoimmune disease. These diseases include type 1 diabetes, lupus, and anaemia, and collectively represent the third commonest cause of morbidity and mortality in humans. The major reason why autoimmunity occurs is thought to be due to a failure in the mechanisms responsible for controlling such unwanted responses. Two other populations of white blood cells are involved in this regulation, termed NK and NKT cells, each of which release important cell hormones. The current project is designed to test whether defects in NK and NKT cells lead to autoimmune disease. For this purpose a special strain of mice (NOD mice) will be used. The reasons for their selection are: 1) they are highly susceptible to a range of autoimmune diseases including diabetes, lupus and anaemia, and 2) we and others have found that they are deficient in both NK and NKT cells. The proposed experiments are divided into two groups, one designed to characterise the nature of the defects in these cells and the other to identify the genes responsible for them. In this way it should be possible to shed light on the genetic basis of autoimmune diseases in general. The approach to be used involves sophisticated techniques of genetic analysis, which require production of special congenic lines of mice. These mice are like NOD mice but carry in addition to NOD genes genetic regions from a non-autoimmune strain with the potential to correct the defects in NK and NKT cells. In this way, it should be possible to pinpoint the disease susceptibility genes involved in causation of autoimmunity and to work out how they affect NK and NKT cells.
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