Understanding Immunopathogenesis of Hepatitis B Virus

了解乙型肝炎病毒的免疫发病机制

• 批准号: 7589684
• 负责人: JODY L BARON
• 金额: $ 36.79万
• 依托单位: UNIVERSITY OF CALIFORNIA, SAN FRANCISCO
• 依托单位国家: 美国
• 财政年份: 2006
• 资助国家: 美国
• 起止时间: 2006-03-01 至 2011-02-28
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/7589684
• 关键词: Acute; Antigen-Presenting Cells; Biological Assay; Cells; Chronic; Chronic Hepatitis; Chronic Hepatitis B; Chronic Phase; Cirrhosis; Dendritic Cells; Disease; Disease Outcome; Disease model; Hepadnaviridae; Hepatic; Hepatitis; Hepatitis B Virus; Human; Hybridomas; Immune; Immune response; Immune system; Immunotherapy; In Vitro; Infection; Injury; Ligands; Liver; Liver diseases; Mediating; Modeling; Mus; Natural Killer Cells; Pathogenesis; Pathologic; Pathology; Primary carcinoma of the liver cells; Process; Resolution; Role; Simian B disease; System; Testing; Transgenic Animals; Transgenic Mice; Viral; Viral Antigens; Virus; Virus Diseases; Virus Replication; cytokine; design; in vitro Model; in vivo; killer T cell; model design; mouse model; pathogen; prevent; response

Hepatitis B Virus (HBV)is a hepadnavirus that is a major cause of acute and chronic hepatitis in humans. Three hundred million people globally are chronically infected with HBV, making HBV one of the most common human pathogens. HBV replication is not cytopathic, and evidence has shown that hepatic pathology is immune-mediated. Thus, understanding the pathogenesis of acute and chronic hepatitis B virus infection mandates understanding the immune responses underlying these processes. Natural hepadnaviral infections occur only in humans and other outbred species whose immune systems are poorly characterized and difficult to study. This proposal seeks to use a new transgenic mouse model of hepatitis B virus infection to identify mechanisms involved in immunopathogenesis of acute and chronic hepatitis B virus infection, including understanding the role of the innate immune response in these disease processes. It is our hope that in identifying mechanisms underlying these disease processes, we will be able to design specific immunotherapies to prevent and treat HBV-related liver disease. Our specific aims are: 1. To determine the mechanism by which non-classical NKT cells mediate acute experimental hepatitis in our transgenic mouse model of primary HBV infection; 2. To test the hypothesis that the early activation of non-classical NKT cells and/or NK Cells in our model of primary HBV infection can significantly influence the chronic phase of hepatitis in our disease model; and 3. To develop an in vitro model of non-classical NKT cell activation in response to Hepatitis B virus, which will establish a fundamental experimental system for identifying the mechanisms of non-classical NKT cell activation.

B型肝炎病毒（HBV）是一种嗜肝DNA病毒，是人类急性和慢性肝炎的主要原因。 全球有3亿人慢性感染HBV，使HBV成为最严重的疾病之一。 常见的人类病原体 HBV复制不是致细胞病变的，有证据表明肝脏病理是免疫介导的。 因此，了解急性和慢性B型肝炎病毒感染的发病机制， 了解这些过程背后的免疫反应。天然嗜肝DNA病毒感染发生在 只有在人类和其他远系繁殖的物种中，其免疫系统的特征很差， study. 这项建议旨在使用一种新的转基因小鼠模型的肝炎B病毒感染，以确定 急性和慢性B型肝炎病毒感染的免疫发病机制，包括 了解先天免疫反应在这些疾病过程中的作用。我们希望， 通过识别这些疾病过程的潜在机制，我们将能够设计具体的 免疫疗法预防和治疗HBV相关肝病。我们的具体目标是：1.确定 非经典NKT细胞介导转基因小鼠急性实验性肝炎的机制 原发性HBV感染模型; 2.为了验证非经典NKT细胞的早期激活 和/或NK细胞在我们的原发性HBV感染模型中可以显著影响HBV感染的慢性期， 我们疾病模型中的肝炎;和3.建立一种非经典NKT细胞活化的体外模型， 对B型肝炎病毒的反应，这将建立一个基本的实验系统，用于确定 非经典NKT细胞活化机制。