Department of Microbiology, NYU Grossman School of Medicine, New York, NY, USA.
NYU Langone Vaccine Center and Department of Medicine, NYU Grossman School of Medicine, New York, NY, USA.
Cell Rep. 2022 Jan 11;38(2):110237. doi: 10.1016/j.celrep.2021.110237. Epub 2021 Dec 21.
Recently identified severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) variants Mu and C.1.2 have spike proteins with mutations that may confer resistance to natural and vaccine-elicited antibodies. Analysis of neutralizing antibody titers in the sera of vaccinated individuals without previous history of infection and from convalescent individuals show partial resistance of the viruses. In contrast, sera from individuals with a previous history of SARS-CoV-2 infection who were subsequently vaccinated neutralize variants with titers 4- to 11-fold higher, providing a rationale for vaccination of individuals with previous infection. The heavily mutated C.1.2 spike is the most antibody neutralization-resistant spike to date; however, the avidity of C.1.2 spike protein for angiotensin-converting enzyme 2 (ACE2) is low. This finding suggests that the virus evolved to escape the humoral response but has a decrease in fitness, suggesting that it may cause milder disease or be less transmissible. It may be difficult for the spike protein to evolve to escape neutralizing antibodies while maintaining high affinity for ACE2.
最近发现的严重急性呼吸综合征冠状病毒 2(SARS-CoV-2)变种 Mu 和 C.1.2 的刺突蛋白具有可能导致对天然和疫苗诱导的抗体产生抗性的突变。对未感染过先前病史的疫苗接种者和康复者血清中的中和抗体滴度进行分析表明,病毒具有部分抗性。相比之下,先前感染过 SARS-CoV-2 的个体的血清在随后接种疫苗时,中和变异体的滴度高 4-11 倍,这为先前感染的个体接种疫苗提供了依据。刺突高度突变的 C.1.2 是迄今为止对抗体中和抗性最强的刺突;然而,C.1.2 刺突蛋白与血管紧张素转换酶 2(ACE2)的亲和力较低。这一发现表明,病毒进化以逃避体液反应,但适应性降低,表明它可能引起较轻的疾病或传染性降低。刺突蛋白可能很难在保持对 ACE2 的高亲和力的同时进化以逃避中和抗体。