Roth Kristian Daniel Ralph, Wenzel Esther Veronika, Ruschig Maximilian, Steinke Stephan, Langreder Nora, Heine Philip Alexander, Schneider Kai-Thomas, Ballmann Rico, Fühner Viola, Kuhn Philipp, Schirrmann Thomas, Frenzel André, Dübel Stefan, Schubert Maren, Moreira Gustavo Marçal Schmidt Garcia, Bertoglio Federico, Russo Giulio, Hust Michael
Institut für Biochemie, Biotechnologie und Bioinformatik, Abteilung Biotechnologie, Technische Universität Braunschweig, Braunschweig, Germany.
Abcalis GmbH, Braunschweig, Germany.
Front Cell Infect Microbiol. 2021 Jul 7;11:697876. doi: 10.3389/fcimb.2021.697876. eCollection 2021.
Antibodies are essential molecules for diagnosis and treatment of diseases caused by pathogens and their toxins. Antibodies were integrated in our medical repertoire against infectious diseases more than hundred years ago by using animal sera to treat tetanus and diphtheria. In these days, most developed therapeutic antibodies target cancer or autoimmune diseases. The COVID-19 pandemic was a reminder about the importance of antibodies for therapy against infectious diseases. While monoclonal antibodies could be generated by hybridoma technology since the 70ies of the former century, nowadays antibody phage display, among other display technologies, is robustly established to discover new human monoclonal antibodies. Phage display is an technology which confers the potential for generating antibodies from universal libraries against any conceivable molecule of sufficient size and omits the limitations of the immune systems. If convalescent patients or immunized/infected animals are available, it is possible to construct immune phage display libraries to select affinity-matured antibodies. A further advantage is the availability of the DNA sequence encoding the phage displayed antibody fragment, which is packaged in the phage particles. Therefore, the selected antibody fragments can be rapidly further engineered in any needed antibody format according to the requirements of the final application. In this review, we present an overview of phage display derived recombinant antibodies against bacterial, viral and eukaryotic pathogens, as well as microbial toxins, intended for diagnostic and therapeutic applications.
抗体是用于诊断和治疗由病原体及其毒素引起的疾病的重要分子。一百多年前,我们就通过使用动物血清治疗破伤风和白喉,将抗体纳入了针对传染病的医疗方法中。如今,大多数已开发的治疗性抗体都靶向癌症或自身免疫性疾病。新冠疫情提醒了人们抗体在治疗传染病方面的重要性。自上世纪70年代以来,虽然可以通过杂交瘤技术产生单克隆抗体,但如今,除其他展示技术外,抗体噬菌体展示技术已牢固确立,用于发现新的人源单克隆抗体。噬菌体展示是一种技术,它有潜力从通用文库中产生针对任何具有足够大小的可想象分子的抗体,并且克服了免疫系统的局限性。如果有康复患者或免疫/感染动物,就有可能构建免疫噬菌体展示文库来筛选亲和力成熟的抗体。另一个优点是可获得编码噬菌体展示抗体片段的DNA序列,该序列包装在噬菌体颗粒中。因此,可以根据最终应用的要求,以任何所需的抗体形式快速对所选抗体片段进行进一步工程改造。在这篇综述中,我们概述了源自噬菌体展示的重组抗体,这些抗体针对细菌、病毒和真核病原体以及微生物毒素,用于诊断和治疗应用。