Brinkkemper Mitch, Veth Tim S, Brouwer Philip J M, Turner Hannah, Poniman Meliawati, Burger Judith A, Bouhuijs Joey H, Olijhoek Wouter, Bontjer Ilja, Snitselaar Jonne L, Caniels Tom G, van der Linden Cynthia A, Ravichandran Rashmi, Villaudy Julien, van der Velden Yme U, Sliepen Kwinten, van Gils Marit J, Ward Andrew B, King Neil P, Heck Albert J R, Sanders Rogier W
Amsterdam UMC, location University of Amsterdam, Department of Medical Microbiology and Infection Prevention, Laboratory of Experimental Virology, Meibergdreef 9, 1105 AZ Amsterdam, the Netherlands.
Amsterdam Institute for Infection and Immunity, Infectious Diseases, Amsterdam, the Netherlands.
iScience. 2022 Dec 22;25(12):105649. doi: 10.1016/j.isci.2022.105649. Epub 2022 Nov 22.
The emergence of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) variants poses continuous challenges in combating the virus. Here, we describe vaccination strategies to broaden SARS-CoV-2 and sarbecovirus immunity by combining spike proteins based on different viruses or viral strains displayed on two-component protein nanoparticles. First, we combined spike proteins based on ancestral and Beta SARS-CoV-2 strains to broaden SARS-CoV-2 immune responses. Inclusion of Beta spike improved neutralizing antibody responses against SARS-CoV-2 Beta, Gamma, and Omicron BA.1 and BA.4/5. A third vaccination with ancestral SARS-CoV-2 spike also improved cross-neutralizing antibody responses against SARS-CoV-2 variants, in particular against the Omicron sublineages. Second, we combined SARS-CoV and SARS-CoV-2 spike proteins to broaden sarbecovirus immune responses. Adding SARS-CoV spike to a SARS-CoV-2 spike vaccine improved neutralizing responses against SARS-CoV and SARS-like bat sarbecoviruses SHC014 and WIV1. These results should inform the development of broadly active SARS-CoV-2 and pan-sarbecovirus vaccines and highlight the versatility of two-component nanoparticles for displaying diverse antigens.
严重急性呼吸综合征冠状病毒2(SARS-CoV-2)变体的出现给抗击该病毒带来了持续挑战。在此,我们描述了通过将基于不同病毒或病毒株的刺突蛋白展示在双组分蛋白质纳米颗粒上,来拓宽SARS-CoV-2和沙贝病毒免疫力的疫苗接种策略。首先,我们将基于原始毒株和贝塔SARS-CoV-2毒株的刺突蛋白组合起来,以拓宽针对SARS-CoV-2的免疫反应。加入贝塔刺突蛋白可改善针对SARS-CoV-2贝塔、伽马和奥密克戎BA.1及BA.4/5的中和抗体反应。用原始SARS-CoV-2刺突蛋白进行第三次疫苗接种也改善了针对SARS-CoV-2变体,特别是针对奥密克戎亚谱系的交叉中和抗体反应。其次,我们将SARS-CoV和SARS-CoV-2刺突蛋白组合起来,以拓宽沙贝病毒的免疫反应。在SARS-CoV-2刺突蛋白疫苗中添加SARS-CoV刺突蛋白可改善针对SARS-CoV以及类似SARS的蝙蝠沙贝病毒SHC014和WIV1的中和反应。这些结果应为广泛有效的SARS-CoV-2疫苗和泛沙贝病毒疫苗的开发提供参考,并突出双组分纳米颗粒展示多种抗原的多功能性。