Department of Epidemiology and Prevention, Center for Clinical Sciences, National Center for Global Health and Medicine, Tokyo, Japan.
Department of Laboratory Testing, Center Hospital of the National Center for the Global Health and Medicine, Tokyo, Japan.
Clin Microbiol Infect. 2023 Sep;29(9):1201.e1-1201.e5. doi: 10.1016/j.cmi.2023.05.020. Epub 2023 May 24.
To examine the differences in durability and its determinants of humoral immunity following 2- and 3-dose COVID-19 vaccination.
Throughout the pandemic, we evaluated the anti-spike IgG antibody titers of 2- and 3-dose mRNA vaccine recipients over time among the staff of a medical and research center in Tokyo. Linear mixed models were used to estimate trajectories of antibody titers from 14 to 180 days after the last immune-conferred event (vaccination or infection) and compare antibody waning rates across prior infection and vaccination status, and across background factors in infection-naïve participants.
A total of 6901 measurements from 2964 participants (median age, 35 years; 30% male) were analyzed. Antibody waning rate (percentage per 30 days [95% CI]) was slower after 3 doses (25% [23-26]) than 2 doses (36% [35-37]). Participants with hybrid immunity (vaccination and infection) had further slower waning rates: 2-dose plus infection (16% [9-22]); 3-dose plus infection (21% [17-25]). Older age, male sex, obesity, coexisting diseases, immunosuppressant use, smoking, and alcohol drinking were associated with lower antibody titers, whereas these associations disappeared after 3 doses, except for sex (lower in female participants) and immunosuppressant use. Antibody waned slightly faster in older participants, females, and alcohol drinkers after 2 doses, whereas it did not differ after 3 doses across except sex.
The 3-dose mRNA vaccine conferred higher durable antibody titers, and previous infection modestly enhanced its durability. The antibody levels at a given time point and waning speed after 2 doses differed across background factors; however, these differences mostly diminished after 3 doses.
研究 2 剂和 3 剂 COVID-19 疫苗接种后体液免疫的持久性及其决定因素的差异。
在整个大流行期间,我们评估了东京一家医疗和研究中心工作人员在最后一次免疫接种(接种或感染)后 14 至 180 天内,2 剂和 3 剂 mRNA 疫苗接种者的抗刺突 IgG 抗体滴度随时间的变化情况。线性混合模型用于估计从最后一次免疫接种(接种或感染)后 14 至 180 天内的抗体滴度轨迹,并比较既往感染和接种状态以及感染前未感染者背景因素对抗体衰减率的影响。
共分析了 2964 名参与者的 6901 次测量结果(中位数年龄为 35 岁,30%为男性)。与 2 剂(36%[35-37])相比,3 剂(25%[23-26])后抗体衰减率(每 30 天的百分比[95%CI])较慢。具有混合免疫(接种和感染)的参与者具有进一步较慢的衰减率:2 剂加感染(16%[9-22]);3 剂加感染(21%[17-25])。年龄较大、男性、肥胖、并存疾病、免疫抑制剂使用、吸烟和饮酒与较低的抗体滴度相关,但这些关联在接种 3 剂后除性别(女性参与者较低)和免疫抑制剂使用外均消失。与 2 剂相比,在接种 3 剂后,年龄较大的参与者、女性和饮酒者的抗体衰减速度略有加快,但除性别外,在接种 3 剂后,各年龄组之间的差异并不明显。
3 剂 mRNA 疫苗可产生更高的持久抗体滴度,既往感染可适度增强其持久性。在 2 剂时,各背景因素之间的抗体水平和衰减速度存在差异,但在接种 3 剂后,这些差异大多消失。