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奥密克戎 BA.5 流行期间,日本针对有症状的 SARS-CoV-2 感染和严重疾病,对单价 mRNA COVID-19 疫苗进行初级系列、首次和第二次加强接种的效果:SARS-CoV-2 疫苗有效性实时监测(VERSUS)。

Effectiveness of primary series, first, and second booster vaccination of monovalent mRNA COVID-19 vaccines against symptomatic SARS-CoV-2 infections and severe diseases during the SARS-CoV-2 omicron BA.5 epidemic in Japan: vaccine effectiveness real-time surveillance for SARS-CoV-2 (VERSUS).

机构信息

Department of Respiratory Infections, Institute of Tropical Medicine, Nagasaki University, Nagasaki, Japan.

Department of Clinical Tropical Medicine, Nagasaki University Graduate School of Biomedical Sciences, Nagasaki, Japan.

出版信息

Expert Rev Vaccines. 2024 Jan-Dec;23(1):213-225. doi: 10.1080/14760584.2024.2310807. Epub 2024 Feb 8.

Abstract

BACKGROUND

This study aimed to evaluate VE of primary, first, and second booster ancestral-strain monovalent mRNA COVID-19 vaccination against symptomatic infections and severe diseases in Japan.

METHODS

We conducted a test-negative case-control study. We included medically attended episodes and hospitalizations involving individuals aged 16 with signs and symptoms from July to November 2022, when Omicron BA.5 was dominant nationwide. To evaluate VE, we calculated adjusted ORs of vaccination among test-positive versus test-negative individuals using a mixed-effects logistic regression.

RESULTS

For VE against symptomatic infections among individuals aged 16 to 59, VE of primary vaccination at > 180 days was 26.1% (95% CI: 10.6-38.8%); VE of the first booster was 58.5% (48.4-66.7%) at 90 days, decreasing to 41.1% (29.5-50.8%) at 91 to 180 days. For individuals aged 60, VE of the first booster was 42.8% (1.7-66.7%) at 90 days, dropping to 15.4% (-25.9-43.2%) at 91 to 180 days, and then increasing to 44.0% (16.4-62.5%) after the second booster. For VE against severe diseases, VE of the first and second booster was 77.3% (61.2-86.7%) at 90 days and 55.9% (23.4-74.6%) afterward.

CONCLUSION

mRNA booster vaccination provided moderate protection against symptomatic infections and high-level protection against severe diseases during the BA.5 epidemic in Japan.

摘要

背景

本研究旨在评估日本针对有症状感染和严重疾病的初级、第一和第二剂原始株单价 mRNA COVID-19 疫苗的 VE。

方法

我们进行了一项病例对照研究。我们纳入了 2022 年 7 月至 11 月期间出现症状和体征的、年龄在 16 岁及以上的有医疗需求的发作和住院病例,当时全国性流行的是奥密克戎 BA.5。为了评估 VE,我们使用混合效应逻辑回归计算了在有症状感染者中,疫苗接种者与未感染者的校正比值比(OR)。

结果

对于 16 至 59 岁人群的有症状感染 VE,180 天以上初级接种的 VE 为 26.1%(95%CI:10.6-38.8%);90 天第一剂加强针的 VE 为 58.5%(48.4-66.7%),91-180 天下降至 41.1%(29.5-50.8%)。对于 60 岁人群,90 天第一剂加强针的 VE 为 42.8%(1.7-66.7%),91-180 天下降至 15.4%(-25.9-43.2%),第二剂加强针后增加至 44.0%(16.4-62.5%)。对于严重疾病 VE,第一剂和第二剂加强针的 VE 为 90 天的 77.3%(61.2-86.7%)和之后的 55.9%(23.4-74.6%)。

结论

在日本 BA.5 流行期间,mRNA 加强针接种为有症状感染提供了适度的保护,为严重疾病提供了高水平的保护。

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