Roederer Alex L, Cao Yi, St Denis Kerri, Sheehan Maegan L, Li Chia Jung, Lam Evan C, Gregory David J, Poznansky Mark C, Iafrate A John, Canaday David H, Gravenstein Stefan, Garcia-Beltran Wilfredo F, Balazs Alejandro B
Ragon Institute of MGH, MIT, and Harvard, Cambridge, MA 02139, USA.
Vaccine and Immunotherapy Center, Massachusetts General Hospital, Boston, MA 02129, USA; Pediatric Infectious Disease, Massachusetts General Hospital for Children, Boston, MA 02114, USA.
Cell Rep Med. 2024 Dec 17;5(12):101850. doi: 10.1016/j.xcrm.2024.101850. Epub 2024 Dec 9.
With the onset of the COVID-19 pandemic 4 years ago, viral sequencing continues to document numerous individual mutations in the viral spike protein across many variants. To determine the ability of vaccine-mediated humoral immunity to combat continued SARS-CoV-2 evolution, we construct a comprehensive panel of pseudoviruses harboring each individual mutation spanning 4 years of the pandemic to understand the fitness cost and resistance benefits of each. These efforts identify numerous mutations that escape from vaccine-induced humoral immunity. Across 50 variants and 131 mutants we construct, we observe progressive loss of neutralization across variants, irrespective of vaccine doses, as well as increasing infectivity and ACE2 binding. Importantly, the recent XBB.1.5 booster significantly increases titers against most variants but not JN.1, KP.2, or KP.3. These findings demonstrate that variants continue to evade updated mRNA vaccines, highlighting the need for different approaches to control SARS-CoV-2 transmission.
4年前随着新冠疫情的爆发,病毒测序持续记录了许多变体中病毒刺突蛋白的大量个体突变。为了确定疫苗介导的体液免疫对抗持续的新冠病毒进化的能力,我们构建了一组全面的假病毒,这些假病毒包含了疫情4年期间的每个个体突变,以了解每个突变的适应性代价和抗性益处。这些研究确定了许多逃避疫苗诱导体液免疫的突变。在我们构建的50个变体和131个突变体中,我们观察到无论疫苗剂量如何,各变体的中和作用都在逐渐丧失,同时传染性和与血管紧张素转换酶2(ACE2)的结合能力也在增强。重要的是,最近的XBB.1.5加强针显著提高了针对大多数变体的抗体滴度,但对JN.1、KP.2或KP.3无效。这些发现表明,变体继续逃避更新后的mRNA疫苗,凸显了需要采用不同方法来控制新冠病毒传播。