Choi Min Joo, Hyun Hakjun, Heo Jung Yeon, Seo Yu Bin, Noh Ji Yun, Cheong Hee Jin, Kim Woo Joo, Kim Hwa Jung, Choi Ju-Yeon, Lee Young Jae, Chung Eun Joo, Kim Su-Hwan, Jeong Hyeonji, Kim Byoungguk, Song Joon Young
Department of Internal Medicine, International St. Mary's Hospital, Catholic Kwandong University College of Medicine, Incheon, Republic of Korea.
Department of Infectious Diseases, Ajou University School of Medicine, Suwon, Republic of Korea.
Heliyon. 2024 Feb 29;10(5):e27211. doi: 10.1016/j.heliyon.2024.e27211. eCollection 2024 Mar 15.
Data on the durability of booster dose immunity of COVID-19 vaccines are relatively limited.
Immunogenicity was evaluated for up to 9-12 months after the third dose of vaccination in 94 healthy adults.
Following the third dose, the anti-spike immunoglobulin G (IgG) antibody response against the wild-type was boosted markedly, which decreased gradually over time. However, even 9-12 months after the booster dose, both the median and geometric mean of anti-spike IgG antibody levels were higher than those measured 4 weeks after the second dose. Breakthrough infection during the Omicron-dominant period boosted neutralizing antibody titers against Omicron sublineages (BA.1 and BA.5) and the ancestral strain. T-cell immune response was efficiently induced and maintained during the study period.
mRNA vaccine booster dose elicited durable humoral immunity for up to 1 year after the third dose and T-cell immunity was sustained during the study period, supporting an annual COVID-19 vaccination strategy.
关于新冠病毒疫苗加强剂量免疫持久性的数据相对有限。
对94名健康成年人在接种第三剂疫苗后长达9至12个月的免疫原性进行了评估。
接种第三剂后,针对野生型的抗刺突免疫球蛋白G(IgG)抗体反应显著增强,且随时间逐渐下降。然而,即使在加强剂量后9至12个月,抗刺突IgG抗体水平的中位数和几何平均数仍高于第二剂接种后4周测得的水平。在奥密克戎占主导的时期发生的突破性感染提高了针对奥密克戎亚谱系(BA.1和BA.5)以及原始毒株的中和抗体滴度。在研究期间,T细胞免疫反应得到有效诱导并维持。
mRNA疫苗加强剂量在第三剂后长达1年引发了持久的体液免疫,并且在研究期间T细胞免疫得以维持,这支持了每年进行新冠病毒疫苗接种的策略。