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在高疫苗接种的亚洲环境中,针对 Delta、Omicron BA.1 和 BA.2 的疫苗有效性:一项病例对照研究。

Vaccine effectiveness against Delta, Omicron BA.1, and BA.2 in a highly vaccinated Asian setting: a test-negative design study.

机构信息

Ministry of Health, Singapore.

Ministry of Health, Singapore.

出版信息

Clin Microbiol Infect. 2023 Jan;29(1):101-106. doi: 10.1016/j.cmi.2022.08.002. Epub 2022 Aug 24.

Abstract

OBJECTIVES

We compared the vaccine effectiveness over time of the primary series and booster against infection and severe disease with the Delta, Omicron BA.1, and BA.2 variants in Singapore, an Asian setting with high vaccination coverage.

METHODS

We conducted a test-negative case-control study on all adult residents in Singapore who underwent PCR testing for severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) in acute hospitals. Individuals with a negative PCR from 1 September, 2021, to 30 November, 2021, and 1 December, 2021, to 25 April, 2022, served as controls for the Delta and Omicron variants respectively, and PCR-positive individuals within these two time periods served as cases. Associations between vaccination status and SARS-CoV-2 infection and severe disease with the Delta or Omicron variants were measured using Poisson regressions. Vaccine effectiveness was calculated by taking 1 minus risk ratio.

RESULTS

There were 68 114 individuals comprising 58 495 controls and 9619 cases for the Delta period, of whom 53 093 completed the primary series and 9161 were boosted. For the Omicron period, 104 601 individuals comprising 80 428 controls, 8643 BA.1 cases, and 15 530 BA.2 cases were included, of whom 29 183 and 71 513 were vaccinated with the primary series and boosted, respectively. The primary series provided greater protection against infection with Delta (45%, 95% CI 40-50%) than against infection with Omicron (21%, 95% CI 7-34% for BA.1; 18%, 95% CI 6-29% for BA.2) at <2 months from vaccination. Vaccine effectiveness of the booster was similar against infection with BA.1 (44%, 95% CI 38-50%) and BA.2 (40%, 95% CI 35-40%). Protection against severe disease by the booster for BA.1 (83%, 95% CI 76-88%) and BA.2 (78%, 95% CI 73-82%) was comparable to that by the primary series for Delta (80%, 95% CI 73-85%).

CONCLUSION

Our findings support the use of a booster dose to reduce the risk of severe disease and mitigate the impact on the healthcare system in an Omicron-predominant epidemic.

摘要

目的

我们比较了在接种疫苗的基础上,加强针在新加坡(一个疫苗接种率较高的亚洲地区)对感染和严重疾病的保护效果,比较的对象是原始株、德尔塔(Delta)、奥密克戎 BA.1 和 BA.2 变异株。

方法

我们对在新加坡急性医院接受严重急性呼吸系统综合征冠状病毒 2(SARS-CoV-2)PCR 检测的所有成年居民进行了一项病例对照研究。2021 年 9 月 1 日至 11 月 30 日和 12 月 1 日至 2022 年 4 月 25 日期间 PCR 检测结果为阴性的个体分别作为德尔塔变异株和奥密克戎变异株的对照组,在此期间 PCR 检测结果为阳性的个体作为病例。使用泊松回归法衡量疫苗接种状态与 SARS-CoV-2 感染和严重疾病与德尔塔或奥密克戎变异株之间的关系。疫苗有效性通过取风险比的倒数计算得出。

结果

德尔塔时期共有 68114 人,其中包括 58495 名对照者和 9619 名病例,其中 53093 人完成了基础系列接种,9161 人进行了加强针接种。奥密克戎时期共有 104601 人,其中包括 80428 名对照者、8643 名 BA.1 病例和 15530 名 BA.2 病例,其中 29183 人和 71513 人分别接种了基础系列和加强针。基础系列对 Delta 变异株的感染保护效果(45%,95%CI 40-50%)优于对奥密克戎变异株的感染保护效果(BA.1 为 21%,95%CI 7-34%;BA.2 为 18%,95%CI 6-29%),从接种疫苗到发病的时间小于 2 个月。加强针在 BA.1(44%,95%CI 38-50%)和 BA.2(40%,95%CI 35-40%)的感染保护效果与原始株相当。加强针对 BA.1(83%,95%CI 76-88%)和 BA.2(78%,95%CI 73-82%)引起的严重疾病的保护效果与基础系列对 Delta(80%,95%CI 73-85%)相当。

结论

我们的研究结果支持使用加强针来降低严重疾病的风险,并减轻奥密克戎为主的流行期间对医疗系统的影响。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1857/9398552/2ba101db9d0f/gr1_lrg.jpg

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