Moyo-Gwete Thandeka, Madzivhandila Mashudu, Makhado Zanele, Ayres Frances, Mhlanga Donald, Oosthuysen Brent, Lambson Bronwen E, Kgagudi Prudence, Tegally Houriiyah, Iranzadeh Arash, Doolabh Deelan, Tyers Lynn, Chinhoyi Lionel R, Mennen Mathilda, Skelem Sango, Marais Gert, Wibmer Constantinos Kurt, Bhiman Jinal N, Ueckermann Veronica, Rossouw Theresa, Boswell Michael, de Oliveira Tulio, Williamson Carolyn, Burgers Wendy A, Ntusi Ntobeko, Morris Lynn, Moore Penny L
National Institute for Communicable Diseases of the National Health Laboratory Service, Johannesburg, South Africa.
Antibody Immunity Research Unit, School of Pathology, Faculty of Health Sciences, University of the Witwatersrand, Johannesburg, South Africa.
bioRxiv. 2021 Mar 11:2021.03.06.434193. doi: 10.1101/2021.03.06.434193.
Neutralization escape by SARS-CoV-2 variants, as has been observed in the 501Y.V2 (B.1.351) variant, has impacted the efficacy of first generation COVID-19 vaccines. Here, the antibody response to the 501Y.V2 variant was examined in a cohort of patients hospitalized with COVID-19 in early 2021 - when over 90% of infections in South Africa were attributed to 501Y.V2. Robust binding and neutralizing antibody titers to the 501Y.V2 variant were detected and these binding antibodies showed high levels of cross-reactivity for the original variant, from the first wave. In contrast to an earlier study where sera from individuals infected with the original variant showed dramatically reduced potency against 501Y.V2, sera from 501Y.V2-infected patients maintained good cross-reactivity against viruses from the first wave. Furthermore, sera from 501Y.V2-infected patients also neutralized the 501Y.V3 (P.1) variant first described in Brazil, and now circulating globally. Collectively these data suggest that the antibody response in patients infected with 501Y.V2 has a broad specificity and that vaccines designed with the 501Y.V2 sequence may elicit more cross-reactive responses.
正如在501Y.V2(B.1.351)变体中所观察到的那样,SARS-CoV-2变体的中和逃逸影响了第一代新冠疫苗的效力。在此,对2021年初因新冠住院的一组患者针对501Y.V2变体的抗体反应进行了检测——当时南非超过90%的感染归因于501Y.V2。检测到针对501Y.V2变体的强大结合和中和抗体滴度,并且这些结合抗体对第一波原始变体表现出高水平的交叉反应性。与早期一项研究不同,在该研究中感染原始变体的个体血清对501Y.V2的效力显著降低,而感染501Y.V2的患者血清对第一波病毒保持良好的交叉反应性。此外,感染501Y.V2的患者血清还能中和最初在巴西发现、现已在全球传播的501Y.V3(P.1)变体。总体而言,这些数据表明感染501Y.V2的患者中的抗体反应具有广泛的特异性,并且以501Y.V2序列设计的疫苗可能引发更多的交叉反应性应答。