Therapeutic Monoclonal Antibodies to H5N1 Influenza

H5N1 流感治疗性单克隆抗体

• 批准号: 7900034
• 负责人: RICHARD John WEBBY
• 金额: $ 343.54万
• 依托单位: ST. JUDE CHILDREN'S RESEARCH HOSPITAL
• 依托单位国家: 美国
• 财政年份: 2006
• 资助国家: 美国
• 起止时间: 2006-07-15 至 2012-06-30
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/7900034
• 关键词: Affinity; Antibodies; Asia; Asians; B-Lymphocytes; Biochemical; Birds; Development; Disease Outbreaks; Domestic Fowls; Elderly; Epitopes; Escape Mutant; Ferrets; Generations; Goals; Human; Human Virology; Hybridomas; Immunity; Immunization; Immunocompromised Host; In Vitro; Infant; Infection; Influenza; Influenza A Virus, H5N1 Subtype; Influenza A virus; Influenza Therapeutic; International Agencies; Lead; Modeling; Monoclonal Antibodies; Mus; National Institute of Allergy and Infectious Disease; Peripheral; Phase; Population; Prevention; Production; Property; Public Health; Research; Strategic Planning; Therapeutic; Therapeutic Monoclonal Antibodies; Treatment Efficacy; Vaccinated; Vaccination; Vaccine Clinical Trial; Vaccines; Variant; Viral load measurement; Virus; anti-influenza; anti-influenza drug; experience; human monoclonal antibodies; humanized antibody; humanized monoclonal antibodies; immunoprophylaxis; in vivo; influenza outbreak; influenzavirus; killings; mortality; neutralizing monoclonal antibodies; novel strategies; pandemic disease; pandemic influenza; prevent; product development; prototype; response; volunteer

DESCRIPTION (provided by applicant): The natural emergence or intentional release of a pandemic influenza virus has the potential to have catastrophic consequences for global public health. This is no better illustrated than by the 1918 Spanish influenza pandemic that swept the globe killing upwards of 50 million people. Although the mortality from subsequent pandemics has not been of this magnitude, other highly pathogenic influenza A viruses circulate in avian reservoirs. One such highly pathogenic virus, H5N1, is now entrenched in many regions of Asia and is growing in geographic range and numbers of hosts infected. Millions of poultry have been slaughtered in unsuccessful attempts to contain this virus. H5N1 infections in this outbreak have been confirmed in 116 humans of which 60 have been fatal. This situation has forced national and international agencies to develop strategic plans for a potential pandemic influenza outbreak. Most of these plans include the stockpiling of currently available anti-influenza drugs as well as the development of new ones. We propose to develop broadly cross-neutralizing monoclonal antibodies (MAbs) specific for H5N1 influenza viruses. This project brings together expertise in H5N1 virology, human MAb production, humanized MAb production and product development. Our approach will be to produce humanized and human (derived from vaccinees in the ongoing NIAID sponsored H5N1 vaccine clinical trials) MAbs capable of neutralizing most if not all Asian H5N1 strains. Antigenic analysis of murine MAbs and our experience with human MAbs demonstrate that broadly reactive MAbs can be made against drift variants of H5N1. This feasibility is shown with the recent isolation of a broadly neutralizing H5N1 MAb. A large panel of H5N1 MAbs will be generated, screened in vitro and in vivo for neutralizing activity, and then affinity matured. From these studies a lead product candidate will be selected for product development. The product will contain two MAbs to minimize escape mutants and to maximize neutralizing potency. We will also employ novel strategies for the production of second generation antibodies with unique properties. The lead antibodies and the second generation antibodies will be characterized in murine and ferret models of H5N1 infection to determine their therapeutic efficacy. The results of these studies will be the development of an effective, highly cross-reactive anti-influenza therapeutic for prevention and potentially for treatment of H5N1 infections.

描述（由申请方提供）：大流行性流感病毒的自然出现或故意释放有可能对全球公共卫生造成灾难性后果。1918年席卷地球仪、造成5 000多万人死亡的西班牙流感大流行就是最好的例证。尽管随后的大流行的死亡率没有达到这种程度，但其他高致病性甲型流感病毒在禽类宿主中传播。其中一种高致病性病毒，H5N1，目前已在亚洲许多地区根深蒂固，其地理范围和受感染宿主的数量都在增加。数百万家禽被宰杀，试图控制这种病毒的努力失败。在这次疫情中，已确认116人感染H5N1，其中60人死亡。这种情况迫使国家和国际机构为潜在的大流行性流感爆发制定战略计划。这些计划大多包括储存现有的抗流感药物以及开发新的药物。我们建议开发具有广泛交叉中和性的H5N1流感病毒特异性单克隆抗体（MAbs）。该项目汇集了H5N1病毒学、人单克隆抗体生产、人源化单克隆抗体生产和产品开发方面的专业知识。我们的方法将是生产人源化和人（来自正在进行的NIAID赞助的H5N1疫苗临床试验中的疫苗接种者）单克隆抗体，能够中和大多数（如果不是所有）亚洲H5N1毒株。鼠单克隆抗体的抗原性分析和我们用人单克隆抗体的经验表明，广泛反应的单克隆抗体可以针对H5N1的漂移变体。最近分离出的一种广泛中和的H5N1单克隆抗体显示了这种可行性。将产生大量H5N1单克隆抗体，在体外和体内筛选中和活性，然后进行亲和力成熟。将从这些研究中选择一种主要候选产品进行产品开发。该产品将含有两种单克隆抗体，以最大限度地减少逃逸突变体并最大限度地提高中和效力。我们还将采用新的策略来生产具有独特特性的第二代抗体。先导抗体和第二代抗体将在H5N1感染的鼠和雪貂模型中表征，以确定其治疗功效。这些研究的结果将是开发一种有效的、高交叉反应性的抗流感治疗药物，用于预防和治疗H5N1感染。

项目成果

An anti-H5N1 influenza virus FcDART antibody is a highly efficacious therapeutic agent and prophylactic against H5N1 influenza virus infection.

抗H5N1流感病毒FcDART抗体是针对H5N1流感病毒感染的高效治疗剂和预防剂。

• DOI: 10.1128/jvi.00078-15
• 发表时间: 2015
• 期刊: Journal of virology
• 影响因子: 5.4
• 作者: Zanin,Mark;Keck,Zhen-Yong;Rainey,GJonah;Lam,Chia-YingKao;Boon,AdrianusCM;Rubrum,Adam;Darnell,Daniel;Wong,Sook-San;Griffin,Yolanda;Xia,Jinming;Webster,RobertG;Webby,Richard;Johnson,Syd;Foung,Steven
• 通讯作者: Foung,Steven