Department of Pathology & Laboratory Medicine, King Hussein Cancer Center, Amman, Jordan.
Department of Pathology & Laboratory Medicine, King Hussein Cancer Center, Amman, Jordan.
Vaccine. 2022 May 3;40(20):2841-2847. doi: 10.1016/j.vaccine.2022.03.069. Epub 2022 Apr 1.
Little is known about the efficacy and durability of anti-RBD IgG antibodies induced by certain SARS-CoV-2 vaccines. It has been shown that neutralizing antibodies are associated with the protection against re-infection. This study aims to compare the mean titers, duration, and efficacy of generating protective anti-RBD IgG antibody response among recipients of Pfizer/BioNTech, AstraZeneca, Sputnik V, Johnson & Johnson, Moderna, and Sinopharm COVID-19 vaccines. In addition, we aimed to compare the susceptibility of getting COVID-19 breakthrough infections after various types of vaccines.
Samples from 2065 blood bank donors and healthcare workers at King Hussein Cancer Center (KHCC) were collected between February and September 2021. Anti-Spike/RBD IgG levels were measured using Chemiluminescent microparticle-immunoassay (CMIA) (ARCHITECT IgG II Quant test, Abbott, USA).
The mean titer of anti-RBD IgG levels was significantly diverse among different types of vaccines. The highest titer level was seen in participants who took a third booster vaccine shot, followed by Pfizer/BioNTech, AstraZeneca, and Sinopharm vaccine. The mean titer levels of anti-RBD IgG antibodies in the Pfizer vaccinated group was the highest after vaccination but started to drop after 60 days from vaccination unlike AstraZeneca and Sinopharm vaccine-induced antibodies where the mean titers continued to be stable until 120 days but their levels were significantly lower. Most of the breakthrough infections were among the Sinopharm vaccinated group and these breakthroughs happened at random times for the three main types of vaccines.
Our data demonstrate that the mean-titer of anti-RBD IgG levels drop after four months which is the best time to take the additional booster shot from a more potent vaccine type such as mRNA vaccines that might be needed in Jordan and worldwide.
目前对于某些 SARS-CoV-2 疫苗诱导的抗 RBD IgG 抗体的疗效和持久性知之甚少。已表明,中和抗体与防止再次感染有关。本研究旨在比较辉瑞/生物技术、阿斯利康、卫星 V、强生、莫德纳和科兴 COVID-19 疫苗接种者产生保护性抗 RBD IgG 抗体反应的平均滴度、持续时间和疗效。此外,我们旨在比较各种类型的疫苗接种后 COVID-19 突破性感染的易感性。
2021 年 2 月至 9 月,在侯赛因国王癌症中心(KHCC)采集了 2065 名血库献血者和医护人员的样本。使用化学发光微粒子免疫测定法(CMIA)(ARCHITECT IgG II Quant 测试,雅培,美国)测量抗尖峰/RBD IgG 水平。
不同类型疫苗的抗 RBD IgG 水平平均滴度差异显著。接受第三剂加强疫苗接种的参与者滴度最高,其次是辉瑞/生物技术、阿斯利康和科兴疫苗。接种辉瑞疫苗后,抗 RBD IgG 抗体的平均滴度最高,但在接种后 60 天开始下降,而阿斯利康和科兴疫苗诱导的抗体则不同,其平均滴度持续稳定至 120 天,但水平显著较低。大多数突破性感染发生在科兴疫苗接种者中,这三种主要类型的疫苗的突破性感染发生时间随机。
我们的数据表明,抗 RBD IgG 水平的平均滴度在四个月后下降,这是接种更有效疫苗类型(如需要在约旦和全球范围内使用的 mRNA 疫苗)的最佳时间接种额外加强针。