The Biodesign Institute, Arizona State University, Tempe, Arizona, USA.
School of Life Sciences, Arizona State University, Tempe, Arizona, USA.
Plant Biotechnol J. 2023 Mar;21(3):549-559. doi: 10.1111/pbi.13970. Epub 2022 Dec 16.
This study describes a novel, neutralizing monoclonal antibody (mAb), 11D7, discovered by mouse immunization and hybridoma generation, against the parental Wuhan-Hu-1 RBD of SARS-CoV-2. We further developed this mAb into a chimeric human IgG and recombinantly expressed it in plants to produce a mAb with human-like, highly homogenous N-linked glycans that has potential to impart greater potency and safety as a therapeutic. The epitope of 11D7 was mapped by competitive binding with well-characterized mAbs, suggesting that it is a Class 4 RBD-binding mAb that binds to the RBD outside the ACE2 binding site. Of note, 11D7 maintains recognition against the B.1.1.529 (Omicron) RBD, as well neutralizing activity. We also provide evidence that this novel mAb may be useful in providing additional synergy to established antibody cocktails, such as Evusheld™ containing the antibodies tixagevimab and cilgavimab, against the Omicron variant. Taken together, 11D7 is a unique mAb that neutralizes SARS-CoV-2 through a mechanism that is not typical among developed therapeutic mAbs and by being produced in ΔXFT Nicotiana benthamiana plants, highlights the potential of plants to be an economic and safety-friendly alternative platform for generating mAbs to address the evolving SARS-CoV-2 crisis.
这项研究描述了一种新型的中和单克隆抗体(mAb)11D7,它是通过对小鼠进行免疫和杂交瘤生成而发现的,针对的是 SARS-CoV-2 的亲本 Wuhan-Hu-1 RBD。我们进一步将该 mAb 开发成嵌合人 IgG,并在植物中重组表达,产生一种具有类似人源、高度均一的 N 连接聚糖的 mAb,具有作为治疗药物增强效力和安全性的潜力。通过与经过充分表征的 mAb 的竞争结合,确定了 11D7 的表位,表明它是一种结合 ACE2 结合位点之外 RBD 的 Class 4 RBD 结合 mAb。值得注意的是,11D7 保持对 B.1.1.529(Omicron)RBD 的识别和中和活性。我们还提供了证据表明,这种新型 mAb 可能有助于为已建立的抗体鸡尾酒提供额外的协同作用,例如含有抗体 tixagevimab 和 cilgavimab 的 Evusheld™,对抗 Omicron 变体。综上所述,11D7 是一种独特的 mAb,通过一种非典型的机制中和 SARS-CoV-2,并且通过在ΔXFT 毕赤酵母中生产,突出了植物作为产生 mAb 的经济和安全友好型替代平台的潜力,以应对不断演变的 SARS-CoV-2 危机。