Improved control of SARS-CoV-2 infection with nucleocapsid-specific antibodies

P. Penaloza-MacMaster, Tanushree Dangi, Sarah Sanchez, Jacob Class, M. Richner, L. Visvabharathy, Young Rock Chung, Kirsten Bentley, R. Stanton, I. Koralnik, Justin M. Richner, P. Penaloza-MacMaster
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Abstract

The severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) spike protein is the main antigen in all approved COVID-19 vaccines and is also the only target for monoclonal antibody (mAb) therapies. Immune responses to other viral antigens are generated after SARS-CoV-2 infection, but their contribution to the antiviral response remains unclear. Here, we interrogated whether nucleocapsid-specific antibodies can improve protection against SARS-CoV-2. We first immunized mice with a nucleocapsid-based vaccine and then transferred sera from these mice into naive mice, followed by challenge with SARS-CoV-2. We show that mice that received nucleocapsid-specific sera or a nucleocapsid-specific mAb exhibited enhanced control of SARS-CoV-2. Nucleocapsid-specific antibodies elicited NK-mediated, antibody-dependent cellular cytotoxicity (ADCC) against infected cells. To our knowledge, these findings provide the first demonstration in the coronavirus literature that antibody responses specific to the nucleocapsid protein can improve viral clearance, providing a rationale for the clinical evaluation of nucleocapsid-based mAb therapies to treat COVID-19. NIH (DP2DA051912)
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核衣壳蛋白特异性抗体改善对SARS-CoV-2感染的控制
严重急性呼吸综合征冠状病毒2 (SARS-CoV-2)刺突蛋白是所有已批准的COVID-19疫苗中的主要抗原,也是单克隆抗体(mAb)治疗的唯一靶点。对其他病毒抗原的免疫反应在SARS-CoV-2感染后产生,但它们对抗病毒反应的贡献尚不清楚。在这里,我们询问核衣壳特异性抗体是否可以提高对SARS-CoV-2的保护。我们首先用基于核衣壳的疫苗对小鼠进行免疫,然后将这些小鼠的血清转移到幼稚小鼠体内,然后用SARS-CoV-2攻击。我们发现,接受核衣壳蛋白特异性血清或核衣壳蛋白特异性单抗的小鼠表现出对SARS-CoV-2的增强控制。核衣壳蛋白特异性抗体引发了针对感染细胞的nk介导的抗体依赖性细胞毒性(ADCC)。据我们所知,这些发现首次证明了针对核衣壳蛋白的抗体反应可以提高病毒的清除能力,为临床评估基于核衣壳蛋白的单克隆抗体治疗COVID-19提供了依据。国家卫生研究院(DP2DA051912)
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