Effectiveness of NVX-CoV2373 and BNT162b2 COVID-19 Vaccination in South Korean Adolescents.

IF 2.2 4区 医学 Q3 IMMUNOLOGY
Pediatric Infectious Disease Journal Pub Date : 2025-11-01 Epub Date: 2025-08-27 DOI:10.1097/INF.0000000000004954
Eunseon Gwak, Seung-Ah Choe, Kyuwon Kim, Erdenetuya Bolormaa, Manuela H Gschwend, Jonathan Fix, Muruga Vadivale, Matthew D Rousculp, Young June Choe
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引用次数: 0

Abstract

Background and aims: Adolescents can have severe/chronic outcomes from COVID-19. Real-world data on relative vaccine effectiveness between mRNA- and protein-based vaccines are limited, and more data are needed on disease outcomes in this age group.

Methods: The K-COV-N database, COVID-19 vaccine registry and health insurance claims were retrospectively reviewed to identify adolescents (12- to 18-year-olds) in South Korea who received a homologous primary series of NVX-CoV2373 or BNT162b2 and a heterologous or homologous third vaccine dose. Vaccine recipients were propensity score matched to reduce confounding baseline factors. Adjusted hazard ratios (aHRs) for any medically attended COVID-19 postvaccination (starting 14 days after primary series and 7 days after a third dose) were calculated to assess relative vaccine effectiveness every 30 days through a 180-day risk window.

Results: From February to December 2022, 3174 and 6253 doses of NVX-CoV2373 and BNT162b2, respectively, were administered to South Korean adolescents. Individuals who received NVX-CoV2373 tended to be older, have a disability, and/or have a prior SARS-CoV-2 infection. Propensity score matching resulted in 107 individuals in each primary series group and 701 and 1417 individuals in the NVX-CoV2373 and BNT162b2 third-dose groups, respectively. The aHR (95% CI) for NVX-CoV2373 compared with BNT162b2 for medically attended COVID-19 in the 180-day risk window was 0.57 (0.31-1.05) for the primary series and 0.68 (0.54-0.84) for the third dose.

Conclusions: These results suggest that NVX-CoV2373 may provide more robust protection against medically attended COVID-19 as a third dose, compared with BNT162b2. While the aHR for the primary series also indicated lower risk with NVX-CoV2373, this difference was not statistically significant.

Abstract Image

Abstract Image

韩国青少年COVID-19疫苗NVX-CoV2373和BNT162b2的有效性
背景和目的:青少年可能会因COVID-19而产生严重/慢性后果。关于mRNA和蛋白质疫苗之间相对疫苗有效性的真实数据有限,需要更多关于该年龄组疾病结局的数据。方法:回顾性分析韩国K-COV-N数据库、COVID-19疫苗登记和健康保险索赔,以确定接受同源NVX-CoV2373或BNT162b2系列初级疫苗和异源或同源第三剂疫苗的青少年(12- 18岁)。疫苗接种者倾向评分匹配,以减少混杂基线因素。通过180天的风险窗口,计算任何接受医疗治疗的COVID-19疫苗接种后(从第一次接种后14天开始和第三次接种后7天开始)的调整风险比(ahr),每30天评估一次疫苗的相对有效性。结果:2022年2月至12月,韩国青少年分别接种了3174剂NVX-CoV2373和6253剂BNT162b2。接受NVX-CoV2373治疗的个体往往年龄较大、有残疾和/或先前感染过SARS-CoV-2。倾向评分匹配结果显示,每个主要系列组有107人,NVX-CoV2373和BNT162b2第三剂量组分别有701人和1417人。在180天的风险窗口中,NVX-CoV2373与BNT162b2在治疗COVID-19时的aHR (95% CI)为0.57(0.31-1.05),第三剂为0.68(0.54-0.84)。结论:这些结果表明,与BNT162b2相比,NVX-CoV2373作为第三剂可能提供更强大的保护,以抵御医疗护理中的COVID-19。虽然初级系列的aHR也表明NVX-CoV2373的风险较低,但这种差异没有统计学意义。
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来源期刊
CiteScore
6.30
自引率
2.80%
发文量
566
审稿时长
2-4 weeks
期刊介绍: ​​The Pediatric Infectious Disease Journal® (PIDJ) is a complete, up-to-the-minute resource on infectious diseases in children. Through a mix of original studies, informative review articles, and unique case reports, PIDJ delivers the latest insights on combating disease in children — from state-of-the-art diagnostic techniques to the most effective drug therapies and other treatment protocols. It is a resource that can improve patient care and stimulate your personal research.
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