Department of Medicine, Shenzhen Ellen-Sven Precision Medicine Institute, Shenzhen, China.
Department of Gastrointestinal Surgery, Renmin Hospital of Wuhan University, Wuhan, Hubei, China.
Viral Immunol. 2023 Apr;36(3):153-162. doi: 10.1089/vim.2022.0094. Epub 2023 Mar 21.
We investigated the persistence of SARS-CoV-2-specific neutralizing antibodies in serum (CoV-2-SNAb) against the "WH-Human 1" coronavirus in 57 convalescent persons from January 2020 to January 2021. The CoV-2-SNAb response against authentic "WH-Human 1" showed a significant ( < 0.01) neutralizing high effect (≥95%) in the following manner: by 94.7% neutralization for up to 6 months, by 73.1% for up to 8 months, and by 31.7% for up to 10 months in correlation with a significant decrease in the concentration of the virus determined by SARS-CoV-2 spike protein extracellular domain and spike-receptor-binding domain (S-RBD). There was neutralizing effect (<95%) when the S-RBD optical density (OD) value was more than 1.0, showing a suitable threshold of S-RBD = 1.0 (antibody-tittering, OD). However, in some convalescent persons, no neutralizing effect (<95%) was observed although the SARS-CoV-2-specific neutralizing antibodies were bound to the S-RBD (OD >1.0). The neutralization of the virus in these cases may not involve S-RBD, but rather B- and T cell memory responses in overall immunity, using the threshold value (OD = 1.0) of S-RBD as a simple and effective method to determine the neutralization effect of the antibody efficacy and use of vaccination in combination with a standard pseudovirus neutralizing assay. We suggest that convalescent persons should contact their physicians 6-month postinfection to test the function of their serum neutralizing antibodies and determine whether administering a SARS-CoV-2 vaccine is necessary to prevent the development of severe illness in the future.
我们调查了 57 名 2020 年 1 月至 2021 年 1 月期间的康复者血清中针对“WH-Human 1”冠状病毒的 SARS-CoV-2 特异性中和抗体(CoV-2-SNAb)的持久性。CoV-2-SNAb 对真实的“WH-Human 1”的反应表现出显著的中和高效应(≥95%),方式如下:在 6 个月内,中和率为 94.7%;在 8 个月内,中和率为 73.1%;在 10 个月内,中和率为 31.7%,这与 SARS-CoV-2 刺突蛋白外域和刺突受体结合域(S-RBD)测定的病毒浓度显著下降相关。当 S-RBD 光密度(OD)值大于 1.0 时,出现中和效应(<95%),表明 S-RBD=1.0(抗体滴度,OD)是一个合适的阈值。然而,在一些康复者中,尽管 SARS-CoV-2 特异性中和抗体与 S-RBD 结合(OD>1.0),但未观察到中和效应(<95%)。在这些情况下,病毒的中和作用可能不涉及 S-RBD,而是涉及整体免疫中的 B 细胞和 T 细胞记忆反应,使用 S-RBD 的阈值(OD=1.0)作为一种简单有效的方法来确定抗体疗效的中和作用,并结合标准假病毒中和试验进行疫苗接种。我们建议,康复者在感染后 6 个月应联系医生,检测其血清中和抗体的功能,并确定是否需要接种 SARS-CoV-2 疫苗以防止未来出现严重疾病。