Post genomic structural and functional aspects of antibody in heath and disease

抗体在健康和疾病中的后基因组结构和功能方面

基本信息

批准号：
121465-2007
负责人：
Kaushik, Azad
金额：
$ 1.56万
依托单位：
University of Guelph
依托单位国家：
加拿大
项目类别：
Discovery Grants Program - Individual
财政年份：
2009
资助国家：
加拿大
起止时间：
2009-01-01 至 2010-12-31
项目状态：
已结题

来源：
https://www.nserc-crsng.gc.ca/ase-oro/Details-Detailles_eng.asp?id=421962
关键词：
Post genomic structural functional aspects

项目摘要

For host defence, disease prevention and therapy, knowledge of the immune system and its regulation in health and disease is of fundamental importance. Towards this goal, our research is focused on 'antibody genetics and autoimmunity'. We made an original discovery of unique functional IgM antibodies in cattle, the largest known to exist in a species. This offers opportunity to develop novel antibody engineering strategies for prevention of those diseases where conventional therapies fail, e.g., cancer, autoimmune diseases and viral infections. My proposed research aims at defining 'structure-function' relationships of these novel types of antibodies and, also to develop a vaccine against bovine leukemia virus. These studies also involve understanding the development of the neonatal immune system aimed at strengthening the host defence of newborns against infections. Other studies are focused on the origin of autoantibodies that cause systemic autoimmune disease, such as Lupus and arthritis. We have observed that pathogenic autoantibodies originate from the impaired development of the antibody repertoire at newborn stage. The role of B-cell selection in generating systemic autoimmune disease is not well understood. The proposed studies are aimed at identifying the anatomical location where white blood cells (B-cells) producing pathogenic autoantibodies, especially of the IgM type, originate so that these could be targeted for elimination by therapeutic intervention in patients afflicted with autoimmune disease. The IgM autoantibody type is studied since these appear first and initiate autoimmune disease.

对于宿主防御、疾病预防和治疗，了解免疫系统及其对健康和疾病的调节至关重要。为了实现这一目标，我们的研究重点是“抗体遗传学和自身免疫”。我们在牛体内首次发现了独特的功能性 IgM 抗体，这是已知物种中存在的最大抗体。这为开发新的抗体工程策略来预防传统疗法失败的疾病提供了机会，例如癌症、自身免疫性疾病和病毒感染。我提出的研究旨在定义这些新型抗体的“结构-功能”关系，并开发针对牛白血病病毒的疫苗。这些研究还涉及了解新生儿免疫系统的发育，旨在加强新生儿对感染的宿主防御。其他研究集中于引起系统性自身免疫性疾病（例如狼疮和关节炎）的自身抗体的起源。我们观察到致病性自身抗体源于新生儿阶段抗体库发育受损。 B 细胞选择在产生系统性自身免疫性疾病中的作用尚不清楚。拟议的研究旨在确定产生致病性自身抗体（尤其是 IgM 型）的白细胞（B 细胞）的解剖位置，以便通过对患有自身免疫性疾病的患者进行治疗干预来消除这些抗体。研究 IgM 自身抗体类型，因为它们首先出现并引发自身免疫性疾病。