1Department of Infectious Diseases, Asan Medical Center, University of Ulsan College of Medicine, Seoul, Republic of Korea.
2Graduate School of Medical Science and Engineering, Korea Advanced Institute of Science and Technology (KAIST), and Center for Epidemic Preparedness, KAIST, Daejeon, Republic of Korea.
Am J Trop Med Hyg. 2021 Jun 17;105(2):395-400. doi: 10.4269/ajtmh.20-1594.
Data on the longevity of humoral and cell-mediated immune responses against severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) in patients with coronavirus disease 2019 (COVID-19) are limited. We evaluated the detailed kinetics of antibody and T-cell responses at the acute, convalescent, and post-convalescent phases in COVID-19 patients with a wide range of severity. We enrolled patients with COVID-19 prospectively from four hospitals and one community treatment center between February 2020 and January 2021. symptom severity was classified as mild, moderate, or severe/critical. Patient blood samples were collected at 1 week (acute), 1 month (convalescent), and 2 months after symptom onset (post-convalescent). Human SARS-CoV-2 IgG and IgM antibodies were measured using in-house-developed ELISA. The SARS-CoV-2-specific T-cell responses against overlapping peptides of spike proteins and nucleoprotein were measured by interferon-γ enzyme-linked immunospot assays. Twenty-five COVID-19 patients were analyzed (mild, n = 5; moderate, n = 9; severe/critical, n = 11). IgM and IgG antibody responses peaked at 1 month after symptom onset and decreased at 2 months. IgG response levels were significantly greater in the severe/critical group compared with other groups. Interferon-γ-producing T-cell responses increased between 1 week and 1 month after symptom onset, and had a trend toward decreasing at 2 months, but did not show significant differences according to severity. Our data indicate that SARS-CoV-2-specific antibody responses were greater in those with severe symptoms and waned after reaching a peak around 1 month after symptom onset. However, SARS-CoV-2-specific T-cell responses were not significantly different according to symptom severity, and decreased slowly during the post-convalescent phase.
关于 2019 冠状病毒病(COVID-19)患者中针对严重急性呼吸综合征冠状病毒 2(SARS-CoV-2)的体液和细胞介导免疫应答的持久性的数据有限。我们评估了 COVID-19 患者在严重程度不同的急性、恢复期和恢复期后的各个阶段的抗体和 T 细胞应答的详细动力学。我们前瞻性地从四家医院和一家社区治疗中心招募了 COVID-19 患者,时间为 2020 年 2 月至 2021 年 1 月。根据症状严重程度分为轻度、中度和严重/危急。患者血液样本在发病后 1 周(急性)、1 个月(恢复期)和 2 个月(恢复期后)采集。使用内部开发的 ELISA 检测人 SARS-CoV-2 IgG 和 IgM 抗体。通过干扰素-γ酶联免疫斑点分析测定针对刺突蛋白和核蛋白重叠肽的 SARS-CoV-2 特异性 T 细胞反应。分析了 25 例 COVID-19 患者(轻度,n=5;中度,n=9;严重/危急,n=11)。IgM 和 IgG 抗体应答在发病后 1 个月达到峰值,并在 2 个月时下降。严重/危急组的 IgG 反应水平明显高于其他组。发病后 1 周至 1 个月干扰素-γ产生 T 细胞反应增加,2 个月时有下降趋势,但根据严重程度无显著差异。我们的数据表明,严重症状患者的 SARS-CoV-2 特异性抗体反应更大,在发病后 1 个月左右达到峰值后减弱。然而,根据症状严重程度,SARS-CoV-2 特异性 T 细胞反应无显著差异,在恢复期后缓慢下降。