Unité Des Virus Émergents (UVE: Aix-Marseille University - IRD 190 - Inserm 1207), Marseille, France.
Sci Rep. 2022 Jul 23;12(1):12609. doi: 10.1038/s41598-022-16964-z.
The replacement of the Omicron BA.1 variant of SARS-CoV-2 by the BA.2 and the rapid growth of the BA.5 sub lineage, which have both different sets of mutations in the spike glycoprotein, alters the spectrum of activity of therapeutic antibodies currently licensed in the European Union. Using clinical strains of the Omicron BA.2 and BA.5 variants, we compared the neutralising power of monoclonal antibodies against the Omicron BA.1, BA.2 and BA.5 variants, using an ancestral strain (lineage B.1, D614G) and a Delta variant strain as reference. Sotrovimab/Vir-7831 is less active against BA.2 than against BA.1 (fold change reduction ~ 1,4) and even less active against BA.5 (fold change reduction ~ 2.7). Within the Evusheld /AZD7442 cocktail, Cilgavimab/AZD1061 is more active against BA.2 and BA.5 than against BA.1 (fold change increase ~ 32), whilst the very low activity of Tixagevimab/AZD8895 against BA.1 is not enhanced against BA.2 nor BA.5. In total, compared to BA.1, the activity of the Evusheld/AZD7442 is significantly improved against BA.2 while BA.5 is intermediate but closer to BA.2.
SARS-CoV-2 的奥密克戎 BA.1 变体被 BA.2 和 BA.5 亚谱系所取代,这两种变体在刺突糖蛋白上都有不同的突变集,改变了目前在欧盟获得许可的治疗性抗体的作用谱。使用奥密克戎 BA.2 和 BA.5 变体的临床株,我们比较了针对奥密克戎 BA.1、BA.2 和 BA.5 变体的单克隆抗体的中和能力,使用了一个原始株(谱系 B.1、D614G)和一个德尔塔变体株作为参考。 Sotrovimab/Vir-7831 对 BA.2 的活性比对 BA.1 的活性降低约 1.4 倍,对 BA.5 的活性甚至降低约 2.7 倍。在 Evusheld/AZD7442 鸡尾酒中,Cilgavimab/AZD1061 对 BA.2 和 BA.5 的活性比对 BA.1 的活性增加约 32 倍,而 Tixagevimab/AZD8895 对 BA.1 的活性非常低,对 BA.2 和 BA.5 没有增强。总的来说,与 BA.1 相比,Evusheld/AZD7442 的活性对 BA.2 的改善明显,而 BA.5 的活性则介于两者之间,但更接近 BA.2。