Imbrechts Maya, Maes Wim, Ampofo Louanne, Van den Berghe Nathalie, Calcoen Bas, Van Looveren Dominique, Kerstens Winnie, Rasulova Madina, Vercruysse Thomas, Noppen Sam, Abdelnabi Rana, Foo Caroline, Hollevoet Kevin, Maes Piet, Zhang Xin, Jochmans Dirk, Ven Karen, Lammertyn Jeroen, Vanhoorelbeke Karen, Callewaert Nico, De Munter Paul, Schols Dominique, Thibaut Hendrik Jan, Neyts Johan, Declerck Paul, Geukens Nick
KU Leuven, PharmAbs: the KU Leuven Antibody Center, Herestraat 49 box 820, 3000 Leuven, Belgium.
KU Leuven, Department Pharmaceutical and Pharmacological Sciences, Laboratory for Therapeutic and Diagnostic Antibodies, 3000 Leuven, Belgium.
iScience. 2022 Aug 19;25(8):104705. doi: 10.1016/j.isci.2022.104705. Epub 2022 Jul 3.
Treatment with neutralizing monoclonal antibodies (mAbs) against severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) contributes to COVID-19 management. Unfortunately, SARS-CoV-2 variants escape several of these recently approved mAbs, highlighting the need for additional discovery and development. In a convalescent patient with COVID-19, we identified six mAbs, classified in four epitope groups, that potently neutralized SARS-CoV-2 D614G, beta, gamma, and delta infection , with three mAbs neutralizing omicron as well. In hamsters, mAbs 3E6 and 3B8 potently cured infection with SARS-CoV-2 Wuhan, beta, and delta when administered post-viral infection at 5 mg/kg. Even at 0.2 mg/kg, 3B8 still reduced viral titers. Intramuscular delivery of DNA-encoded 3B8 resulted in mAb production of median serum levels up to 90 μg/mL, and protected hamsters against delta infection. Overall, our data mark 3B8 as a promising candidate against COVID-19, and highlight advances in both the identification and gene-based delivery of potent human mAbs.
使用针对严重急性呼吸综合征冠状病毒2(SARS-CoV-2)的中和单克隆抗体(mAb)进行治疗有助于新冠肺炎的管理。不幸的是,SARS-CoV-2变体对几种最近获批的mAb产生了逃逸,这凸显了进一步研发的必要性。在一名新冠肺炎康复患者体内,我们鉴定出六种mAb,分为四个表位组,它们能有效中和SARS-CoV-2 D614G、β、γ和δ毒株感染,其中三种mAb也能中和奥密克戎毒株。在仓鼠实验中,mAb 3E6和3B8在病毒感染后以5mg/kg的剂量给药时,能有效治愈SARS-CoV-2武汉株、β和δ毒株感染。即使剂量为0.2mg/kg,3B8仍能降低病毒滴度。肌肉注射DNA编码的3B8可使血清中mAb的中位水平达到90μg/mL,并保护仓鼠免受δ毒株感染。总体而言,我们的数据表明3B8是一种有前景的抗新冠肺炎候选药物,并突出了在高效人源mAb的鉴定和基于基因的递送方面所取得的进展。