S Amrutha, Kaur Komaldeep, Aggarwal Deepak, Sodhi Mandeep Kaur, Jaswal Shivani, Saini Varinder
Department of Pulmonary Critical Care and Sleep Medicine, Government Medical College and Hospital, Chandigarh.
Department of Biochemistry, Government Medical College and Hospital, Chandigarh.
Monaldi Arch Chest Dis. 2024 Dec 31;94(4). doi: 10.4081/monaldi.2023.2677. Epub 2023 Nov 3.
On March 11, 2020, the World Health Organization declared COVID-19 a pandemic. According to the findings of various studies conducted around the world, the serological response varies greatly among different populations, with the determinants of variable responses still unknown, including the role of disease severity, which is thought to have a definite correlation. The purpose of this study was to assess serial SARS-CoV-2 immunoglobulin G (IgG) antibody response in COVID-19 patients and correlate it with disease severity. This was a longitudinal observational study in which 45 patients (age >18 years) were enrolled who had recovered from COVID-19 and were reporting to the post-COVID Care Outpatient Clinic. Patients who had been on long-term immunosuppressive therapy prior to SARS-CoV-2 infection were not eligible. All patients had not been immunized against SARS-CoV-2 and had no history of contact with recent COVID-19 cases. The patients underwent serial blood tests to determine serum IgG titers specific for SARS-CoV-2 at 30, 60, and 90 days after being diagnosed with COVID-19. Chemiluminescence was used to perform a semi-quantitative evaluation of the SARS-CoV-2 IgG antibody. At 30 days after confirmed SARS-CoV-2 infection, 98.78% had detectable serum IgG levels, and sero-reversion (loss of previously detectable antibodies) occurred in 2.5% at 60 days and 90 days. Serum IgG was found to peak at 30 days out of the three time points of measurement (30, 60, and 90 days from diagnosis). Serum IgG levels at 90 days were significantly lower than those at 30 days (p<0.0001) and 60 days (p=0.002). The current study's findings shed light on the presence and persistence of serum SARS-CoV-2-specific IgG antibodies following a natural infection. The findings point to a long-lasting immune response with increasing severity in the initial COVID-19 disease.
2020年3月11日,世界卫生组织宣布新型冠状病毒肺炎(COVID-19)为大流行病。根据世界各地开展的各种研究结果,不同人群的血清学反应差异很大,反应多变的决定因素仍然未知,包括疾病严重程度的作用,人们认为二者存在一定关联。本研究的目的是评估COVID-19患者中严重急性呼吸综合征冠状病毒2(SARS-CoV-2)免疫球蛋白G(IgG)抗体的系列反应,并将其与疾病严重程度相关联。这是一项纵向观察性研究,纳入了45例(年龄>18岁)从COVID-19中康复并前往COVID-19后护理门诊就诊的患者。在SARS-CoV-2感染前接受长期免疫抑制治疗的患者不符合条件。所有患者均未接种过SARS-CoV-2疫苗,且无近期接触COVID-19病例的病史。患者在被诊断为COVID-19后的30天、60天和90天接受系列血液检测,以确定针对SARS-CoV-2的血清IgG滴度。采用化学发光法对SARS-CoV-2 IgG抗体进行半定量评估。在确诊SARS-CoV-2感染后的30天,98.78%的患者血清IgG水平可检测到,60天和90天时血清转化(先前可检测到的抗体消失)发生率为2.5%。在三个测量时间点(诊断后的30天、60天和90天)中,血清IgG在30天达到峰值。90天时的血清IgG水平显著低于30天(p<0.0001)和60天(p=0.002)。本研究结果揭示了自然感染后血清SARS-CoV-2特异性IgG抗体的存在和持续情况。这些结果表明,在最初的COVID-19疾病中,免疫反应持久且病情越严重反应越强。