NHC Key Laboratory of Biosafety, National Institute for Viral Disease Control and Prevention, Chinese Center for Disease Control and Prevention (China CDC), Beijing, China.
CAS Key Laboratory of Pathogenic Microbiology and Immunology, Institute of Microbiology, Chinese Academy of Sciences, Beijing, China.
Clin Infect Dis. 2022 Aug 24;75(1):e1072-e1081. doi: 10.1093/cid/ciab884.
The longitudinal antigen-specific immunity in COVID-19 convalescents is crucial for long-term protection upon individual re-exposure to SARS-CoV-2, and even more pivotal for ultimately achieving population-level immunity. We conducted this cohort study to better understand the features of immune memory in individuals with different disease severities at 1 year post-disease onset.
We conducted a systematic antigen-specific immune evaluation in 101 COVID-19 convalescents, who had asymptomatic, mild, moderate, or severe disease, through 2 visits at months 6 and 12 after disease onset. The SARS-CoV-2-specific antibodies, comprising neutralizing antibody (NAb), immunoglobulin (Ig) G, and IgM, were assessed by mutually corroborated assays (ie, neutralization, enzyme-linked immunosorbent assay [ELISA], and microparticle chemiluminescence immunoassay [MCLIA]). Meanwhile, T-cell memory against SARS-CoV-2 spike, membrane, and nucleocapsid proteins was tested through enzyme-linked immunospot assay (ELISpot), intracellular cytokine staining, and tetramer staining-based flow cytometry, respectively.
SARS-CoV-2-specific IgG antibodies, and NAb, can persist among >95% of COVID-19 convalescents from 6 to 12 months after disease onset. At least 19/71 (26%) of COVID-19 convalescents (double positive in ELISA and MCLIA) had detectable circulating IgM antibody against SARS-CoV-2 at 12 months post-disease onset. Notably, numbers of convalescents with positive SARS-CoV-2-specific T-cell responses (≥1 of the SARS-CoV-2 antigen S1, S2, M, and N proteins) were 71/76 (93%) and 67/73 (92%) at 6 and 12 months, respectively. Furthermore, both antibody and T-cell memory levels in the convalescents were positively associated with disease severity.
SARS-CoV-2-specific cellular and humoral immunities are durable at least until 1 year after disease onset.
在 COVID-19 康复者中,针对 SARS-CoV-2 的纵向抗原特异性免疫对于个体再次接触 SARS-CoV-2 后的长期保护至关重要,对于最终实现人群水平的免疫力更为关键。我们进行了这项队列研究,以更好地了解疾病发作后 1 年不同疾病严重程度个体的免疫记忆特征。
我们通过在疾病发作后 6 个月和 12 个月进行的 2 次访视,对 101 名无症状、轻症、中度或重症 COVID-19 康复者进行了系统的 SARS-CoV-2 特异性免疫评估。通过相互验证的检测(即中和、酶联免疫吸附测定[ELISA]和微粒子化学发光免疫测定[MCLIA])评估 SARS-CoV-2 特异性抗体,包括中和抗体(NAb)、免疫球蛋白(Ig)G 和 IgM。同时,通过酶联免疫斑点测定(ELISpot)、细胞内细胞因子染色和四聚体染色流式细胞术分别检测针对 SARS-CoV-2 刺突、膜和核衣壳蛋白的 T 细胞记忆。
SARS-CoV-2 特异性 IgG 抗体和 NAb 可在疾病发作后 6 至 12 个月持续存在于超过 95%的 COVID-19 康复者中。在疾病发作后 12 个月,至少有 19/71(26%)的 COVID-19 康复者(ELISA 和 MCLIA 均为阳性)具有可检测的针对 SARS-CoV-2 的循环 IgM 抗体。值得注意的是,在 6 个月和 12 个月时,具有 SARS-CoV-2 特异性 T 细胞反应阳性(S1、S2、M 和 N 蛋白中的 1 种或多种 SARS-CoV-2 抗原)的康复者数量分别为 71/76(93%)和 67/73(92%)。此外,康复者的抗体和 T 细胞记忆水平均与疾病严重程度呈正相关。
SARS-CoV-2 特异性细胞和体液免疫至少在疾病发作后 1 年仍然持久。