Suphanchaimat Rapeepong, Nittayasoot Natthaprang, Jiraphongsa Chuleeporn, Thammawijaya Panithee, Bumrungwong Punsapach, Tulyathan Atthavit, Cheewaruangroj Nontawit, Pittayawonganon Chakkarat, Tharmaphornpilas Piyanit
Division of Epidemiology, Department of Disease Control, Ministry of Public Health, Nonthaburi 11000, Thailand.
International Health Policy Program, Ministry of Public Health, Nonthaburi 11000, Thailand.
Vaccines (Basel). 2022 Jul 5;10(7):1080. doi: 10.3390/vaccines10071080.
The objective of this study is to explore the real-world effectiveness of various vaccine regimens to tackle the epidemic of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) Delta variant in Thailand during September-December 2021. We applied a test-negative case control study, using nationwide records of people tested for SARS-CoV-2. Each case was matched with two controls with respect to age, detection date, and specimen collection site. A conditional logistic regression was performed. Results were presented in the form vaccine effectiveness (VE) and 95% confidence interval. A total of 1,460,458 observations were analyzed. Overall, the two-dose heterologous prime-boost, ChAdOx1 + BNT162b2 and CoronaVac + BNT162b2, manifested the largest protection level (79.9% (74.0-84.5%) and 74.7% (62.8-82.8%)) and remained stable over the whole study course. The three-dose schedules (CoronaVac + CoronaVac + ChAdOx1, and CoronaVac + CoronaVac + BNT162b2) expressed very high degree of VE estimate (above 80.0% at any time interval). Concerning severe infection, almost all regimens displayed very high VE estimate. For the two-dose schedules, heterologous prime-boost regimens seemed to have slightly better protection for severe infection relative to homologous regimens. Campaigns to expedite the rollout of third-dose booster shot should be carried out. Heterologous prime-boost regimens should be considered as an option to enhance protection for the entire population.
本研究的目的是探讨2021年9月至12月期间,泰国采用的各种疫苗接种方案应对严重急性呼吸综合征冠状病毒2(SARS-CoV-2)Delta变异株流行的实际效果。我们采用了一项检测阴性病例对照研究,利用全国范围内SARS-CoV-2检测者的记录。每个病例在年龄、检测日期和样本采集地点方面与两个对照进行匹配。进行了条件逻辑回归分析。结果以疫苗效力(VE)和95%置信区间的形式呈现。共分析了1,460,458条观察数据。总体而言,两剂次异源初免-加强方案,即ChAdOx1 + BNT162b2和科兴疫苗(CoronaVac)+ BNT162b2,表现出最高的保护水平(分别为79.9%(74.0-84.5%)和74.7%(62.8-82.8%)),且在整个研究过程中保持稳定。三剂次接种方案(科兴疫苗+科兴疫苗+ChAdOx1,以及科兴疫苗+科兴疫苗+BNT162b2)的VE估计值非常高(在任何时间间隔均高于80.0%)。对于重症感染,几乎所有接种方案的VE估计值都非常高。对于两剂次接种方案,异源初免-加强方案相对于同源方案似乎对重症感染有稍好的保护作用。应开展加速第三剂加强针接种的活动。异源初免-加强方案应被视为增强全体人群保护的一种选择。