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).

IF 5.5 3区 医学 Q1 IMMUNOLOGY Expert Review of Vaccines Pub Date : 2024-01-01 Epub Date: 2024-02-08 DOI:10.1080/14760584.2024.2310807
Haruka Maeda, Nobuo Saito, Ataru Igarashi, Masayuki Ishida, Mayumi Terada, Shingo Masuda, Ryosuke Osawa, Naoto Hosokawa, Kei Nakashima, Hiroshi Kamura, Haruki Imura, Hiroki Inoue, Suguru Matsuzaka, Yukihiro Sugimoto, Osamu Kuwamitsu, Iori Motohashi, Toru Morikawa, Rentaro Oda, Yuiko Hoshina, Takashi Matono, Osamu Teshigahara, Eiichiro Sando, Sadaharu Asami, Satoshi Kudo, Noboru Akizuki, Yoshikazu Muto, Tomoichiro Hayakawa, Tomoo Kishaba, Yasuji Ohara, Yoshinao Kubo, Motoi Suzuki, Konosuke Morimoto
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引用次数: 0

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.

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在日本 SARS-CoV-2 omicron BA.5 流行期间,接种单价 mRNA COVID-19 疫苗初级系列、第一次和第二次加强接种对无症状 SARS-CoV-2 感染和严重疾病的有效性:SARS-CoV-2 疫苗有效性实时监测 (VERSUS)。
背景:本研究旨在评估在日本接种祖传株单价 mRNA COVID-19 疫苗对无症状感染和严重疾病的预防效果:我们进行了一项试验阴性病例对照研究。我们纳入了 2022 年 7 月至 11 月(当时 Omicron BA.5 在全国占主导地位)有症状和体征的年龄≥16 岁的人的就诊和住院病例。为了评估 VE,我们使用混合效应逻辑回归法计算了检测呈阳性者与检测呈阴性者接种疫苗的调整 OR:对于 16 至 59 岁人群的无症状感染 VE,大于 180 天的初次接种 VE 为 26.1%(95% CI:10.6-38.8%);≤90 天的首次加强接种 VE 为 58.5%(48.4-66.7%),91 至 180 天的 VE 降至 41.1%(29.5-50.8%)。对于年龄≥60 岁的人,第一次加强接种的 VE 在≤90 天时为 42.8%(1.7-66.7%),在 91 至 180 天时降至 15.4%(-25.9-43.2%),第二次加强接种后又增至 44.0%(16.4-62.5%)。结论:在日本 BA.5 疫情期间,接种 mRNA 强毒疫苗可对无症状感染提供中度保护,并对严重疾病提供高度保护。
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来源期刊
Expert Review of Vaccines
Expert Review of Vaccines 医学-免疫学
CiteScore
9.10
自引率
3.20%
发文量
136
审稿时长
4-8 weeks
期刊介绍: Expert Review of Vaccines (ISSN 1476-0584) provides expert commentary on the development, application, and clinical effectiveness of new vaccines. Coverage includes vaccine technology, vaccine adjuvants, prophylactic vaccines, therapeutic vaccines, AIDS vaccines and vaccines for defence against bioterrorism. All articles are subject to rigorous peer-review. The vaccine field has been transformed by recent technological advances, but there remain many challenges in the delivery of cost-effective, safe vaccines. Expert Review of Vaccines facilitates decision making to drive forward this exciting field.
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