Wang Bei, Goh Yun Shan, Prince Tessa, Ngoh Eve Zi Xian, Salleh Siti Nazihah Mohd, Hor Pei Xiang, Loh Chiew Yee, Fong Siew Wai, Hartley Catherine, Tan Seow-Yen, Young Barnaby Edward, Leo Yee-Sin, Lye David C, Maurer-Stroh Sebastian, Ng Lisa F P, Hiscox Julian A, Renia Laurent, Wang Cheng-I
Singapore Immunology Network, Agency for Science, Technology and Research (A*STAR), Singapore, Singapore.
A*STAR Infectious Diseases Labs (A*STAR ID Labs), Agency for Science, Technology and Research (A*STAR), Singapore, Singapore.
NPJ Vaccines. 2021 Oct 25;6(1):125. doi: 10.1038/s41541-021-00389-2.
The rapid spreading of SARS-CoV-2 variants B.1.1.7 originated from the United Kingdom and B.1.351 from South Africa has contributed to the second wave of COVID-19 cases in the respective countries and also around the world. In this study, we employed advanced biochemical and virological methodologies to evaluate the impact of Spike mutations of these strains on the degree of protection afforded by humoral immune responses following natural infection of the ancestral SARS-CoV-2 strain during the early stages of the outbreak. We found that antibody-mediated neutralization activity was partially reduced for B.1.1.7 variant and significantly attenuated for the B.1.351 strain. We also found that mutations outside the receptor-binding domain (RBD) can strongly influence antibody binding and neutralization, cautioning the use of solely RBD mutations in evaluating vaccine efficacy. These findings highlight an urgent need to develop new SARS-CoV-2 vaccines that are not based exclusively on the ancestral SARS-CoV-2 Spike gene sequence.
源自英国的新冠病毒SARS-CoV-2变异株B.1.1.7和源自南非的B.1.351的迅速传播,在各自国家以及全球范围内引发了第二波新冠疫情。在本研究中,我们运用先进的生化和病毒学方法,评估了这些毒株的刺突蛋白突变对在疫情早期阶段自然感染原始SARS-CoV-2毒株后体液免疫反应所提供的保护程度的影响。我们发现,B.1.1.7变异株的抗体介导中和活性部分降低,而B.1.351毒株的中和活性则显著减弱。我们还发现,受体结合域(RBD)之外的突变可强烈影响抗体结合及中和作用,这警示在评估疫苗效力时仅关注RBD突变的做法不可取。这些发现凸显了迫切需要研发并非完全基于原始SARS-CoV-2刺突基因序列的新型SARS-CoV-2疫苗。