Zhou Hao, Dcosta Belinda M, Samanovic Marie I, Mulligan Mark J, Landau Nathaniel R, Tada Takuya
bioRxiv. 2021 Mar 24:2021.03.24.436620. doi: 10.1101/2021.03.24.436620.
DNA sequence analysis recently identified the novel SARS-CoV-2 variant B.1.526 that is spreading at an alarming rate in the New York City area. Two versions of the variant were identified, both with the prevalent D614G mutation in the spike protein together with four novel point mutations and with an E484K or S477N mutation in the receptor binding domain, raising concerns of possible resistance to vaccine-elicited and therapeutic antibodies. We report that convalescent sera and vaccine-elicited antibodies retain full neutralizing titer against the S477N B.1.526 variant and neutralize the E484K version with a modest 3.5-fold decrease in titer as compared to D614G. The E484K version was neutralized with a 12-fold decrease in titer by the REGN10933 monoclonal antibody but the combination cocktail with REGN10987 was fully active. The findings suggest that current vaccines and therapeutic monoclonal antibodies will remain protective against the B.1.526 variants. The findings further support the value of wide-spread vaccination.
DNA序列分析最近鉴定出新型SARS-CoV-2变体B.1.526,该变体正在纽约市地区以惊人的速度传播。已鉴定出该变体的两个版本,两者在刺突蛋白中均具有普遍存在的D614G突变,以及四个新的点突变,并且在受体结合域中具有E484K或S477N突变,这引发了对疫苗诱导的抗体和治疗性抗体可能产生抗性的担忧。我们报告称,康复期血清和疫苗诱导的抗体对S477N B.1.526变体保持完全中和效价,与D614G相比,对E484K版本的中和效价适度降低3.5倍。REGN10933单克隆抗体对E484K版本的中和效价降低了12倍,但与REGN10987的联合鸡尾酒疗法具有完全活性。这些发现表明,目前的疫苗和治疗性单克隆抗体对B.1.526变体仍具有保护作用。这些发现进一步支持了广泛接种疫苗的价值。