异源的
助推器(火箭)
免疫系统
病毒学
免疫学
增强剂量
2019年冠状病毒病(COVID-19)
医学
生物
同源染色体
免疫
传染病(医学专业)
疾病
遗传学
基因
病理
物理
天文
作者
Xin Zhang,Li Li,Yongmei Liu,Haoting Zhan,Muwei Dai,Kun Zhang,Huimin Yan,Huixia Gao,Jingwen Liu,Shifu Liu,Weina Lu,Yongzhe Li,Aidong Feng,Erhei Dai,Junying Zhou
出处
期刊:Viral Immunology
[Mary Ann Liebert, Inc.]
日期:2024-12-01
卷期号:37 (10): 480-488
标识
DOI:10.1089/vim.2024.0076
摘要
Coronavirus disease 2019 (COVID-19), caused by severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) and first identified in Wuhan, China, in December 2019, has led to global efforts in vaccination to mitigate rising morbidity and mortality, with vaccines proving crucial in controlling the pandemic. This study evaluated the humoral responses to the inactivated virus vaccine Sinopharm or Koxing Kerlafor, the protein subunit vaccine ZF001, and the adenoviral vector vaccine Convidecia after 18 months of inactivated virus vaccination by heterologous and homologous booster vaccination in patients with previous SARS-CoV-2 infection and healthy individuals. We discovered that patients who had recovered from the infection and then received a third vaccine dose (booster) exhibited durable immunity. Furthermore, the heterologous booster vaccine induced higher neutralizing antibody responses compared with the homologous booster. These findings offer valuable insights into the efficacy of different COVID-19 vaccine strategies following booster immunization.
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