Department of Pharmaceutical Microbiology, Pharmacy Faculty, Bezmialem Vakıf University, İstanbul, Turkey
Department of Medical Microbiology Faculty, of Medicine, Kırklareli University, Kırklareli, Turkey
Balkan Med J. 2022 May 24;39(3):172-177. doi: 10.4274/balkanmedj.galenos.2022.2021-8-131. Epub 2022 Apr 5.
Monitoring the longevity of immunoglobulin G (IgG) responses following severe acute respiratory syndrome coronavirus-2 (SARS-CoV-2) infections is vital to understanding the role of antibodies in preventing infection.
To determine the quantitative IgG responses specific to the Spike-S1 (S1) receptor-binding domain (S1/RBD) region of the virus in serum samples taken between 4 weeks and 7 months after polymerase chain reaction (PCR) positivity in patients who are diagnosed with coronavirus disease-2019 (COVID-19).
A longitudinal study.
This study included 113 patients with a clinical and molecular diagnosis of COVID-19. The first and second serum samples were taken 1 and 7 months, respectively, after the PCR positivity. S1/RBD-specific IgG antibody response was assayed using anti-SARS-CoV- 2 QuantiVac ELISA (IgG) kit (Euroimmun, Lübeck, Germany). The neutralizing antibodies were investigated in 57 patients whose IgG test results were above the cut-off value.
In 57 patients with SARS-CoV-2 IgG, the anti-SARS-CoV-2 IgG quantitative antibody levels significantly decreased after 7 months (Z = −2.197, = 0.028). A correlation was detected between the anti-SARS-CoV-2 IgG and nAb percent inhibition (IH%) levels detected in 1 month (rs = 0.496, p < 0.001), but without significant correlation in serum samples taken on 7 months. The nAb IH% levels of the first and second were compared for COVID-19 severity and revealed no statistical difference ( = 0.256). In the second serum sample, the nAb IH%s of patients with moderate COVID-19 showed a statistically significant difference from patients with mild COVID-19 ( = 0.018), but without significant differences between severe and moderate or mild COVID-19.
SARS-CoV-2 quantitative IgG antibody titers are significantly reduced at long-term follow-up (> 6 months). Due to the limited information on seroconversion, comprehensive studies should be conducted for long-term follow-up of the immune response against SARS-CoV-2.
监测严重急性呼吸综合征冠状病毒 2(SARS-CoV-2)感染后免疫球蛋白 G(IgG)反应的持久性对于了解抗体在预防感染中的作用至关重要。
确定聚合酶链反应(PCR)阳性后 4 周至 7 个月之间,从诊断为 2019 年冠状病毒病(COVID-19)的患者血清样本中检测到针对病毒的刺突-S1(S1)受体结合域(S1/RBD)区域的定量 IgG 反应。
纵向研究。
本研究纳入了 113 例临床和分子诊断为 COVID-19 的患者。第一次和第二次血清样本分别在 PCR 阳性后 1 个月和 7 个月采集。使用抗 SARS-CoV-2 QuantiVac ELISA(IgG)试剂盒(Euroimmun,吕贝克,德国)检测 S1/RBD 特异性 IgG 抗体反应。在 IgG 检测结果超过临界值的 57 例患者中研究了中和抗体。
在 57 例 SARS-CoV-2 IgG 患者中,7 个月后 SARS-CoV-2 IgG 定量抗体水平显著下降(Z = -2.197, = 0.028)。在 1 个月时检测到的抗 SARS-CoV-2 IgG 和 nAb 百分比抑制(IH%)水平之间检测到相关性(rs = 0.496,p < 0.001),但在 7 个月时血清样本中未检测到相关性。比较 COVID-19 严重程度的第一和第二份血清样本,发现无统计学差异( = 0.256)。在第二份血清样本中,中度 COVID-19 患者的 nAb IH%与轻度 COVID-19 患者有统计学差异( = 0.018),但严重和中度或轻度 COVID-19 患者之间无显著差异。
在长期随访(> 6 个月)中,SARS-CoV-2 定量 IgG 抗体滴度显著降低。由于有关血清转换的信息有限,应进行全面研究以对 SARS-CoV-2 免疫反应进行长期随访。