Mechanisms of broadly neutralizing humoral immunity against influenza viruses

广泛中和流感病毒体液免疫的机制

• 批准号: 8653053
• 负责人: Peter Palese
• 金额: $ 195.31万
• 依托单位: ICAHN SCHOOL OF MEDICINE AT MOUNT SINAI
• 依托单位国家: 美国
• 财政年份: 2014
• 资助国家: 美国
• 起止时间: 2014-04-01 至 2019-03-31
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/8653053
• 关键词: Antibodies; Antigens; B-Lymphocytes; Binding; Blocking Antibodies; Chicago; Communication; Communities; Data; Dissection; Elements; Epidemic; Epitope Mapping; Epitopes; Evolution; Exhibits; Fc Receptor; Fc domain; Generations; Glycoproteins; HN Protein; Hemagglutinin; Human; Humoral Immunities; IgG1; Immune response; Immunity; Immunization; Immunoglobulin Constant Region; Immunoglobulin G; Influenza; Influenza vaccination; Intention; Intervention; Investigation; Knock-in Mouse; Laboratories; Maintenance; Maps; Mediating; Medicine; Membrane; Membrane Glycoproteins; Membrane Proteins; Memory; Microbiology; Molecular; Molecular Genetics; Molecular Immunology; Monoclonal Antibodies; Mouse Strains; Mus; Neuraminidase; Occupational activity of managing finances; Office of Administrative Management; Pathogenesis; Plasmablast; Polysaccharides; Protein Microchips; Reagent; Recombinants; Regulation; Resistance; Resources; Rheumatology; Role; Route; Specificity; System; Therapeutic; Time; Transgenic Animals; Universities; Vaccination; Vaccine Therapy; Vaccines; Viral; Viral Hemagglutinins; Viral Proteins; Virus; Virus Diseases; Work; anti-influenza; base; bindin; design; expression cloning; flu; human subject; improved; influenza virus vaccine; influenzavirus; medical schools; member; neutralizing monoclonal antibodies; pathogen; polyclonal antibody; public health relevance; recombinant virus; response; success; transmission process; vaccine development

DESCRIPTION (provided by applicant): Human vaccines have most often been generated by trial and error with little understanding of molecular mechanisms involved in the protective immunity that they provide. This system of vaccine development has been remarkably effective against pathogens that exhibit little variability over time; however, it has become evident that a much more sophisticated approach is required to develop broadly protective vaccines against pathogens that undergo continuous structural change, such as influenza viruses. Current influenza virus vaccines confer protection by eliciting antibodies that block viral entry by bindin regions of the virus that are highly mutable. In order for antibody-based therapies and vaccines to be effective against a breadth of structurally diverse influenza viruses, protection will clearl have to be gained through alternate routes of blocking viral replication. The identification of broadly neutralizing monoclonal antibodies against the conserved stalk domain of the viral hemagglutinin (HA), by members of our group and by others, was a groundbreaking advance, as many of these antibodies are able to block fusion of viral and endosomal membranes, yet bind epitopes that are relatively resistant to structural change. A second critical finding by members of our group was that protection mediated by anti-stalk antibodies at low concentrations is dependent on Fc-Fc Receptor (FcR) interactions; therefore, antibody isotype determines protective activity of anti-stalk antibodies at lower concentrations. The current proposal is for a multi-center investigation into molecular mechanisms that can be harnessed to provide broad-based protection against influenza viruses. Our projects include: 1) Precise mapping of epitopes on the viral HA and neuraminidase glycoproteins that mediate virus neutralization, and dissection of mechanisms by which they achieve neutralization. 2) Immunization studies using chimeric influenza virus proteins designed to identify structural elements able to mediate broad-spectrum humoral immunity. 3) Delineation of the roles of Fc-FcR interactions in viral neutralization. 4) Investigation in human subjects into how to elicit antibodies with favorable Fc domains during vaccination. 5) Studies on the natural evolution of human B cell specificities against influenza antigens. 6) Identification of specific sequences of influenza antigen exposures that elicit broad-spectrum, anti-influenza humoral immunity. Overall, our intention is to better understand the mechanisms of broadly protective humoral immune responses against the influenza virus surface proteins and thereby create a blueprint for advancing a new generation of broadly protective influenza virus vaccines and antibody-based therapeutics.

描述（由申请人提供）：人类疫苗通常是通过反复试验而产生的，而对它们提供的保护性免疫涉及的分子机制几乎没有理解。这种疫苗开发系统对随着时间的变化几乎没有变化的病原体非常有效。但是，已经很明显的是，需要一种更复杂的方法来开发针对经历连续结构变化的病原体（例如流感病毒）的病原体。当前的流感病毒疫苗通过引起抗体阻断高度可变的病毒区域的病毒进入的抗体，从而允许保护。为了使基于抗体的疗法和疫苗能够有效地抵抗结构多样的流感病毒，必须通过阻止病毒复制的替代途径来获得保护。我们小组成员和其他人的病毒性血凝蛋白（HA）的鉴定，鉴定出针对病毒性血凝素（HA）的保守茎域（HA）的鉴定，这是一项突破性的进步，因为许多这些抗体能够阻止病毒式和内体膜的融合，但具有相关的抗构造性变化。我们小组成员的第二个关键发现是，抗stalk抗体介导的抗浓度下介导的保护取决于FC-FC受体（FCR）相互作用。因此，抗体同种型确定抗stalk抗体在较低浓度下的保护活性。当前的建议是针对可以利用的分子机制进行多中心研究，以提供针对流感病毒的广泛保护。 我们的项目包括：1）在病毒HA和神经氨酸酶糖蛋白上介导病毒中和的糖蛋白上表位的精确映射，并解剖其实现中和的机制。 2）使用嵌合流感病毒蛋白的免疫研究，旨在鉴定能够介导广谱体液免疫的结构元素。 3）描述FC-FCR相互作用在病毒中和的作用。 4）在人类受试者中调查如何在疫苗接种过程中引起有利的FC结构域的抗体。 5）研究人类B细胞特异性针对流感抗原的自然演变。 6）鉴定流感抗原暴露的特定序列，这些暴露会引起广谱，抗激素za的体液免疫。总体而言，我们的目的是更好地了解针对流感病毒表面蛋白的广泛保护性体液免疫反应的机制，从而创造出一种蓝图，以促进新一代广泛保护性流感病毒疫苗和抗体基于抗体的疗法。