Bean David J, Liang Yan Mei, Sagar Manish
Department of Virology, Immunology and Microbiology, Boston University Chobanian & Avedisian School of Medicine; Boston, MA.
Department of Medicine, Boston University Chobanian & Avedisian School of Medicine; Boston, MA.
bioRxiv. 2024 Oct 23:2024.10.23.619886. doi: 10.1101/2024.10.23.619886.
Recent documented infection with an endemic coronavirus (eCoV) associates with less severe coronavirus disease 2019 (COVID-19), yet the immune mechanism behind this protection has not been fully explored. We measured both antibody and T cell responses against severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) in SARS-CoV-2 naïve individuals classified into two groups, either with or without presumed recent eCoV infections. There was no difference in neutralizing antibodies and T cell responses against SARS-CoV-2 antigens between the two groups. SARS-CoV-2 naïve individuals with recent presumed eCoV infection, however, had higher levels of Fc receptor (FcR) binding antibodies against eCoV spikes (S) and SARS-CoV-2 S2. There was also a significant correlation between eCoV and SARS-CoV-2 FcR binding antibodies. Recent eCoV infection boosts cross-reactive antibodies that can mediate Fc effector functions, and this may play a role in the observed heterotypic immune protection against severe COVID-19.
近期记录的地方性冠状病毒(eCoV)感染与症状较轻的2019冠状病毒病(COVID-19)相关,但这种保护背后的免疫机制尚未得到充分探索。我们在未感染严重急性呼吸综合征冠状病毒2(SARS-CoV-2)的个体中测量了针对SARS-CoV-2的抗体和T细胞反应,这些个体被分为两组,一组有近期可能感染eCoV的情况,另一组没有。两组之间针对SARS-CoV-2抗原的中和抗体和T细胞反应没有差异。然而,近期可能感染eCoV的未感染SARS-CoV-2个体针对eCoV刺突(S)和SARS-CoV-2 S2的Fc受体(FcR)结合抗体水平较高。eCoV和SARS-CoV-2 FcR结合抗体之间也存在显著相关性。近期eCoV感染会增强可介导Fc效应功能的交叉反应性抗体,这可能在观察到的针对严重COVID-19的异型免疫保护中发挥作用。