Innate Immune Response to Human Metapneumovirus Infection

对人类偏肺病毒感染的先天免疫反应

• 批准号: 8473152
• 负责人: Antonella Casola
• 金额: $ 35.6万
• 依托单位: UNIVERSITY OF TEXAS MED BR GALVESTON
• 依托单位国家: 美国
• 财政年份: 2010
• 资助国家: 美国
• 起止时间: 2010-06-01 至 2015-05-31
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/8473152
• 关键词: Acute; Affect; Amino Acids; Antigen-Presenting Cells; Antiviral Agents; Antiviral Response; Applications Grants; Asthma; Bronchiolitis; Cell membrane; Cells; Cellular Immunology; Cellular biology; Child; Childhood; Clinical; Communities; Dendritic Cells; Development; Dimerization; Disease; Elderly; Epidemiology; Epithelial Cells; Event; Family; GTP-Binding Proteins; Gene Expression; Genes; Grant; Host Defense; Human; Human Metapneumovirus; Immune; Immune response; Immune system; Immunocompromised Host; In Vitro; Infection; Inflammatory; Inflammatory Response; Interferon Type I; Interferons; Investigation; Lower Respiratory Tract Infection; Lung; Lung Inflammation; Lung diseases; Mediating; Molecular; Molecular Virology; Morbidity - disease rate; Mutation; Nuclear; Pathogenesis; Pathogenicity; Pathway interactions; Patients; Pneumonia; Population; Positioning Attribute; Production; Proteins; Public Health; RNA Helicase; RNA Viruses; Reagent; Recombinants; Relative (related person); Respiratory Tract Infections; Respiratory physiology; Role; Signal Pathway; Signal Transduction; Signaling Molecule; Syndrome; System; T cell response; TLR4 gene; Techniques; Toll-like receptors; Tretinoin; Vaccines; Viral; Viral Proteins; Virulence; Virulence Factors; Virus; Virus Diseases; base; chemokine; cytokine; domain mapping; effective therapy; fighting; flu; glycoprotein G; human metapneumovirus G glycoprotein; in vivo; monocyte; mortality; mouse model; novel therapeutics; pathogen; positional cloning; protein expression; public health relevance; recombinant virus; response; toll-like receptor 4; transcription factor; vaccine candidate; viral RNA

DESCRIPTION (provided by applicant): Acute respiratory tract infections are a leading cause of morbidity and mortality in children worldwide. Human metapneumovirus (hMPV) is a recently identified human pathogen responsible for a significant portion of upper and lower respiratory tract infections not only in children but also in the elderly and in immunocompromised patients. No effective treatment or vaccine for hMPV is currently available and many fundamental questions regarding the pathogenesis of hMPV-induced lung disease and the host immune response have yet to be answered. We have recently found that hMPV glycoprotein G expression potently inhibits type I interferon (IFN) production, as well as secretion of cytokines and chemokine both in vitro and in vivo. This effect occurs via inhibition of viral-induced Nuclear Factor-?B (NF-?B) and Interferon Regulatory Factors (IRF) activation, suggesting a role of G protein in regulating early intracellular signaling events triggered by hMPV infection. Indeed, we found that G protein specifically targets hMPV-induced cellular responses mediated by the cytoplasmic RNA helicase retinoic acid-inducible gene-I (RIG-I) in airway epithelial cells and by Toll-like receptor (TLR)4 in primary immune cells. In this grant, we propose to identify the mechanism(s) by which hMPV G protein inhibits TLR-dependent and -independent cellular signaling and to start defining the role of G protein in modulating innate and adaptive immune responses in vivo. Upon completion of the proposed investigations, we will obtain new critical information regarding the mechanisms of hMPV-induced cellular signaling, which may allow us to specifically modulate viral-induced gene expression and therefore antiviral and innate immune/inflammatory responses. Furthermore, the results obtained from these studies will be instrumental for the development of safer and more effective hMPV vaccines.

描述（由申请方提供）：急性呼吸道感染是全球儿童发病和死亡的主要原因。人偏肺病毒（Human metapneumovirus，hMPV）是近年发现的一种可引起儿童、老年人和免疫功能低下患者上、下呼吸道感染的病原体。目前尚无有效的hMPV治疗方法或疫苗，关于hMPV诱导的肺部疾病的发病机制和宿主免疫应答的许多基本问题尚未得到解答。我们最近发现，hMPV糖蛋白G的表达有效地抑制I型干扰素（IFN）的生产，以及分泌的细胞因子和趋化因子在体外和体内。这种作用是通过抑制病毒诱导的核因子-？B（NF-？B）和干扰素调节因子（IRF）激活，表明G蛋白在调节hMPV感染引发的早期细胞内信号传导事件中的作用。事实上，我们发现G蛋白特异性靶向hMPV诱导的细胞反应，其由气道上皮细胞中的细胞质RNA解旋酶视黄酸诱导基因I（RIG-I）和原代免疫细胞中的Toll样受体（TLR）4介导。在这项研究中，我们提出了确定hMPV G蛋白抑制TLR依赖性和非依赖性细胞信号传导的机制，并开始定义G蛋白在体内调节先天性和适应性免疫应答中的作用。在完成拟议的研究后，我们将获得有关hMPV诱导的细胞信号传导机制的新的关键信息，这可能使我们能够特异性调节病毒诱导的基因表达，从而抗病毒和先天免疫/炎症反应。此外，从这些研究中获得的结果将有助于开发更安全，更有效的hMPV疫苗。