Department of Integrative Structural and Computational Biology, The Scripps Research Institute, 10550 North Torrey Pines Road, La Jolla, CA 92037, USA.
Janssen Research and Development, Spring House, PA 19002, USA.
Science. 2018 Nov 2;362(6414):598-602. doi: 10.1126/science.aaq0620.
Broadly neutralizing antibodies against highly variable pathogens have stimulated the design of vaccines and therapeutics. We report the use of diverse camelid single-domain antibodies to influenza virus hemagglutinin to generate multidomain antibodies with impressive breadth and potency. Multidomain antibody MD3606 protects mice against influenza A and B infection when administered intravenously or expressed locally from a recombinant adeno-associated virus vector. Crystal and single-particle electron microscopy structures of these antibodies with hemagglutinins from influenza A and B viruses reveal binding to highly conserved epitopes. Collectively, our findings demonstrate that multidomain antibodies targeting multiple epitopes exhibit enhanced virus cross-reactivity and potency. In combination with adeno-associated virus-mediated gene delivery, they may provide an effective strategy to prevent infection with influenza virus and other highly variable pathogens.
针对高度变异病原体的广谱中和抗体激发了疫苗和治疗药物的设计。我们报告了使用各种骆驼科单域抗体来针对流感病毒血凝素生成具有令人印象深刻的广度和效力的多域抗体。多域抗体 MD3606 通过静脉内给药或从重组腺相关病毒载体局部表达来保护小鼠免受甲型和乙型流感感染。这些抗体与来自甲型和乙型流感病毒的血凝素的晶体和单颗粒电子显微镜结构揭示了与高度保守表位的结合。总的来说,我们的发现表明,针对多个表位的多域抗体表现出增强的病毒交叉反应性和效力。与腺相关病毒介导的基因传递相结合,它们可能提供一种预防流感病毒和其他高度变异病原体感染的有效策略。