Department of General Practice and Family Medicine, Chulabhorn Hospital, Chulabhorn Royal Academy, Bangkok, Thailand.
Department of Medicine, Chulabhorn Hospital, Chulabhorn Royal Academy, Bangkok, Thailand.
Hum Vaccin Immunother. 2022 Nov 30;18(5):2052525. doi: 10.1080/21645515.2022.2052525. Epub 2022 Mar 24.
Mass vaccination with a safe and effective vaccine may be the best way to control the COVID-19 pandemic. Heterologous prime-boost vaccination with the CoronaVac and AZD1222 vaccines may increase the immunogenicity elicited by either vaccine alone. This study sought to compare the immunogenicity of a heterologous CoronaVac and AZD1222 prime-boost with a homologous CoronaVac prime-boost. From July 13 to September 2, 2021, 88 participants were enrolled in the study. Half (n = 44) of the participants were assigned to the AZD1222/CoronaVac cohort and half were assigned to the CoronaVac/AZD1222 cohort. Both cohorts had a prime-boost interval of 4 weeks. A control group of 136 health care personnel who received the homologous CoronaVac/CoronaVac prime-boost was matched by age and sex to the experimental cohorts. The primary endpoint was the geometric mean ratio (GMR) of the anti-receptor binding domain (RBD) antibody concentration 4 weeks after the booster dose was administered. The CoronaVac/CoronaVac cohort served as the reference group. Baseline age and sex were similar, and the median age was 42.5 years. The GMR was 2.58 (95% confidence interval [CI] 1.80-3.71) and 8.69 (95% CI 6.05-12.47) in the AZD1222/CoronaVac and CoronaVac/AZD1222 cohorts, respectively. Reactogenicity was similar following prime and booster doses with the same vaccine. Findings indicated that the heterologous CoronaVac and AZD1222 prime-boost combination elicited a more robust immune response than the homologous CoronaVac prime-boost. While both heterologous prime-boost combinations showed similar reactogenicity, the immunogenicity of the CoronaVac/AZD1222 cohort was higher, indicating that the order of prime-boost vaccine administration was important.
大规模接种安全有效的疫苗可能是控制 COVID-19 大流行的最佳方法。使用科兴疫苗和阿斯利康疫苗进行异源初免-加强免疫接种可能会提高两种疫苗单独接种引起的免疫原性。本研究旨在比较异源科兴疫苗和阿斯利康疫苗初免-加强与同源科兴疫苗初免-加强的免疫原性。2021 年 7 月 13 日至 9 月 2 日,88 名参与者入组了这项研究。其中一半(n=44)被分配到阿斯利康疫苗/科兴疫苗组,另一半被分配到科兴疫苗/阿斯利康疫苗组。两组的初免-加强间隔均为 4 周。一个由 136 名接受同源科兴疫苗/科兴疫苗初免-加强的医护人员组成的对照组,按照年龄和性别与实验组进行匹配。主要终点是加强针接种后 4 周时抗受体结合域(RBD)抗体浓度的几何平均比(GMR)。科兴疫苗/科兴疫苗组作为参考组。基线年龄和性别相似,中位年龄为 42.5 岁。阿斯利康疫苗/科兴疫苗组和科兴疫苗/阿斯利康疫苗组的 GMR 分别为 2.58(95%置信区间[CI] 1.80-3.71)和 8.69(95%CI 6.05-12.47)。使用相同疫苗进行初免和加强接种后,反应原性相似。结果表明,异源科兴疫苗和阿斯利康疫苗初免-加强组合引起的免疫反应比同源科兴疫苗初免-加强更强烈。虽然两种异源初免-加强组合的反应原性相似,但科兴疫苗/阿斯利康疫苗组的免疫原性更高,表明疫苗接种顺序很重要。