Department of Infectious Diseases, Aarhus University Hospital, Aarhus, Denmark; Department of Clinical Medicine, Aarhus University, Aarhus, Denmark.
Center of Excellence for Health, Immunity and Infections, Rigshospitalet, University of Copenhagen, Copenhagen, Denmark.
Clin Microbiol Infect. 2022 Aug;28(8):1126-1133. doi: 10.1016/j.cmi.2022.03.003. Epub 2022 Mar 11.
To identify individual characteristics associated with serological COVID-19 vaccine responsiveness and the durability of vaccine-induced antibodies.
Adults without history of SARS-CoV-2 infection from the Danish population scheduled for SARS-CoV-2 vaccination were enrolled in this parallel group, phase 4 study. SARS-CoV-2 Spike IgG and Spike-ACE2-receptor-blocking antibodies were measured at days 0, 21, 90, and 180. Vaccine responsiveness was categorized according to Spike IgG and Spike-ACE2-receptor-blocking levels at day 90 after first vaccination. Nondurable vaccine response was defined as day-90 responders who no longer had significant responses by day 180.
Of 6544 participants completing two vaccine doses (median age 64 years; interquartile range: 54-75), 3654 (55.8%) received BTN162b2, 2472 (37.8%) mRNA-1273, and 418 (6.4%) ChAdOx1 followed by an mRNA vaccine. Levels of both types of antibodies increased from baseline to day 90 and then decreased to day 180. The decrease was more pronounced for levels of Spike-ACE2-receptor-blocking antibodies than for Spike IgG. Proportions with vaccine hyporesponsiveness and lack of durable response were 5.0% and 12.1% for Spike IgG and 12.7% and 39.6% for Spike-ACE2-receptor-blocking antibody levels, respectively. Male sex, vaccine type, and number of comorbidities were associated with all four outcomes. Additionally, age ≥75 years was associated with hyporesponsiveness for Spike-ACE2-receptor-blocking antibodies (adjusted odds ratio: 1.59; 95% confidence interval: 1.25-2.01) but not for Spike IgG.
Comorbidity, male sex, and vaccine type were risk factors for hyporesponsiveness and nondurable response to COVID-19 vaccination. The functional activity of vaccine-induced antibodies declined with increasing age and had waned to pre-second-vaccination levels for most individuals after 6 months.
确定与血清 COVID-19 疫苗反应性和疫苗诱导抗体的持久性相关的个体特征。
本平行组、4 期研究纳入了来自丹麦人群、无 SARS-CoV-2 感染史且计划接种 SARS-CoV-2 疫苗的成年人。在第 0、21、90 和 180 天测量 SARS-CoV-2 刺突 IgG 和刺突-血管紧张素转换酶 2(ACE2)受体阻断抗体。根据首次接种后第 90 天的刺突 IgG 和刺突-ACE2 受体阻断水平对疫苗反应性进行分类。无持久疫苗反应定义为第 90 天有反应者,而在第 180 天不再有显著反应。
6544 名完成两剂疫苗接种的参与者(中位年龄 64 岁;四分位间距:54-75)中,3654 名(55.8%)接种了 BNT162b2、2472 名(37.8%)接种了 mRNA-1273,418 名(6.4%)接种了 ChAdOx1 后又接种了 mRNA 疫苗。两种类型的抗体水平均从基线升高至第 90 天,然后下降至第 180 天。刺突-ACE2 受体阻断抗体水平的下降比刺突 IgG 更明显。刺突 IgG 和刺突-ACE2 受体阻断抗体水平的疫苗低反应率和无持久反应率分别为 5.0%和 12.1%、12.7%和 39.6%。男性、疫苗类型和合并症数量与所有四个结局均相关。此外,年龄≥75 岁与刺突-ACE2 受体阻断抗体低反应相关(调整后的优势比:1.59;95%置信区间:1.25-2.01),但与刺突 IgG 无关。
合并症、男性和疫苗类型是 COVID-19 疫苗接种低反应性和无持久反应性的危险因素。疫苗诱导的抗体的功能活性随年龄增长而下降,大多数个体在 6 个月后降至第二次接种前的水平。