Kara Ertan, Tanır Ferdi, Demirhindi Hakan, Mete Burak, Kibar Filiz, Çetiner Salih, Candevir Aslihan, İnaltekin Ayşe
Çukurova University Faculty of Medicine, Department of Public Health, Adana, Türkiye.
Çukurova University Faculty of Medicine, Department of Medical Microbiology, Çukurova University Balcalı Hospital Central Laboratory, Adana, Türkiye.
Mikrobiyol Bul. 2022 Jul;56(3):566-573. doi: 10.5578/mb.20229715.
Vaccination induces the development of long-lasting immunity necessary for a sustained and essential protective antibody response. Understanding how long the humoral immune response induced by the severe acute respiratory syndrome coronavirus-2 (SARS-CoV-2) inactivated vaccine lasts is important to create an effective immunization scheme. This study aimed to detect the first, third, sixth month concentrations and seroconversion rates of the antibodies induced by the inactivated vaccine. The study included 282 healthcare workers who were vaccinated at days 0 and 28 by the inactivated SARS-CoV-2 vaccine (3 μg/0.5ml). Anti-S-RBD-IgG (receptor binding domain) antibody concentrations and seroconversion rates were examined in vaccinated healthcare workers at the first, third and sixth months after the vaccination. MAGLUMI SARS-CoV-2 S-RBD IgG (CLIA) (Snibe Diagnostics, Chinese) kit was used for the detection of antibodies. The mean age of the healthcare workers was 38.93 ± 10.59 (min= 21-max= 64). After the administration of the second vaccine dose, the participants were found to be reactive for anti-SRBD-IgG antibodies by 98.2% and 97.8% at the first and third months, respectively,. The decrease in the mean plasma concentrations of anti-S-RBD IgG was observed as 56.7% in the cohort with only two doses of the vaccine (first month: 42.4 AU/ml versus third month: 18.2 AU/ml). In the cohort with a history of coronavirus disease 2019 (COVID-19) prior to the vaccination, the decrease was observed as 25.1% (first month: 58.29 versus third month: 43.64 AU/ml) and at a mean of 57.4 (0-90) days prior to vaccination, the decrease rate was 43.1% (first month: 55.05 AU/ml versus third month: 31.28 AU/ml), keeping more stable in participants infected at a mean of 183.1 (91-330) days prior to vaccination(a decrease of 5.2%; with 62.34 AU/ml at first and 59.08 AU/ml at third months). At the end of the sixth month, antibodies could not be detected in 16.7% of people who (n= 42) received two doses of the inactivated vaccine, and the amount of anti-S-RDB IgG decreased by an average of 52.5% compared to the third month, and by 74.8% compared to the first month. Antibody concentrations at the first, third, and sixth months after the vaccination with two doses of the inactivated SARS-CoV-2 vaccine were found to be decreased and at the sixth month, the rate of non-reactive people was 16.7%. As participants who had COVID-19 at a mean of 181 (90-330) days before the vaccination presented with a more stable antibody level, it can be concluded that a booster at months 6-12, resulting in a schedule of 0-1-6 months, is recommended for the inactive SARS-CoV-2 vaccination for effective herd immunity.
疫苗接种可诱导产生持久免疫力,这对于持续且必要的保护性抗体反应至关重要。了解严重急性呼吸综合征冠状病毒2(SARS-CoV-2)灭活疫苗诱导的体液免疫反应能持续多久,对于制定有效的免疫方案很重要。本研究旨在检测灭活疫苗诱导的抗体在第1、3、6个月时的浓度及血清转化率。该研究纳入了282名医护人员,他们在第0天和第28天接种了SARS-CoV-2灭活疫苗(3μg/0.5ml)。在接种疫苗后的第1、3和6个月,对已接种疫苗的医护人员检测抗S-RBD-IgG(受体结合域)抗体浓度及血清转化率。使用MAGLUMI SARS-CoV-2 S-RBD IgG(CLIA)(深圳新产业生物医学工程股份有限公司,中国)试剂盒检测抗体。医护人员的平均年龄为38.93±10.59岁(最小21岁 - 最大64岁)。在接种第二剂疫苗后,参与者在第1个月和第3个月时抗SRBD-IgG抗体的反应性分别为98.2%和97.8%。在仅接种两剂疫苗的队列中,观察到抗S-RBD IgG的平均血浆浓度下降了56.7%(第1个月:42.4 AU/ml对比第3个月:18.2 AU/ml)。在接种疫苗前有2019冠状病毒病(COVID-19)病史的队列中,下降幅度为25.1%(第1个月:58.29对比第3个月:43.64 AU/ml),且在接种疫苗前平均57.4(0 - 90)天时,下降率为43.1%(第1个月:55.05 AU/ml对比第3个月:31.28 AU/ml),而在接种疫苗前平均183.1(91 - 330)天时感染的参与者中抗体水平保持更稳定(下降5.2%;第1个月为62.34 AU/ml,第3个月为59.08 AU/ml)。在第6个月末,16.7%(n = 42)接种两剂灭活疫苗的人无法检测到抗体,抗S-RDB IgG的量与第3个月相比平均下降了52.5%,与第1个月相比下降了74.8%。接种两剂SARS-CoV-2灭活疫苗后第1、3和6个月的抗体浓度下降,且在第6个月时,无反应者的比例为16.7%。由于在接种疫苗前平均181(90 - 330)天感染过COVID-19的参与者抗体水平更稳定,因此可以得出结论,对于SARS-CoV-2灭活疫苗接种,建议在6 - 12个月时加强免疫,形成0 - 1 - 6个月的接种程序,以实现有效的群体免疫。