Baakliny Maryo, Ghosn Nada, Saleh Nadine, Maison Patrick
Université Paris-Est Créteil Val de Marne, Créteil, France.
Epidemiological Surveillance Unit, Ministry of Public Health, Beirut, Lebanon.
PLoS One. 2025 Mar 20;20(3):e0318344. doi: 10.1371/journal.pone.0318344. eCollection 2025.
The emergence of the novel severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) and the subsequent coronavirus disease 2019 (COVID-19) pandemic with the continuous evolution of the virus into variants such as Alpha, Beta, Delta, Omicron and others necessitates an on-going surveillance and evaluation of vaccine effectiveness (VE).This study focuses on assessing the real-world performance of the Pfizer-BioNTech (BNT162b2) vaccine against the Omicron variant. This study employs a test-negative, case-control design, a methodology commonly utilized for estimating the VE in influenza studies. It evaluates SARS-CoV-2 test results in individuals aged 50 and older who had influenza-like illness (ILI) or COVID-like illness (CLI) symptoms and presented to the sentinel sites, classifying positive cases as "cases" and negative as "controls." Data collection was done through a standardized questionnaire administered by the Epidemiological Surveillance Unit (ESU) COVID-19 team via phone interviews. Logistic regression analysis was performed to measure the association, taking into account all confounding factors. The results indicate a 14% VE against contracting the disease among fully vaccinated individuals. Factors such as age and underlying conditions significantly influenced VE. The findings of this study highlight the effectiveness of the Pfizer-BioNTech (BNT162b2) vaccine in reducing the odds of symptomatic COVID-19, particularly by decreasing the prevalence of key symptoms such as fever, cough, myalgia, and loss of taste or smell. Breakthrough infections still occurred, indicating that while the vaccine reduces symptom severity, it may not fully prevent infection This VE is lower compared to previous variants, indicating potential challenges in vaccine efficacy. The study underscores the need for an on-going monitoring and potential booster doses to enhance protection, especially against evolving variants like Omicron.
新型严重急性呼吸综合征冠状病毒2(SARS-CoV-2)的出现以及随后的2019冠状病毒病(COVID-19)大流行,随着病毒不断演变成诸如阿尔法、贝塔、德尔塔、奥密克戎等变体,有必要持续监测和评估疫苗效力(VE)。本研究聚焦于评估辉瑞-生物科技公司(BNT162b2)疫苗针对奥密克戎变体的实际效果。本研究采用检测阴性的病例对照设计,这是一种在流感研究中常用于估计疫苗效力的方法。它评估了年龄在50岁及以上、有流感样疾病(ILI)或新冠样疾病(CLI)症状并前往哨点的个体的SARS-CoV-2检测结果,将阳性病例分类为“病例”,阴性病例分类为“对照”。数据收集通过流行病学监测股(ESU)COVID-19团队通过电话访谈发放的标准化问卷进行。进行逻辑回归分析以衡量这种关联,同时考虑所有混杂因素。结果表明,在完全接种疫苗的个体中,预防感染该疾病的疫苗效力为14%。年龄和基础疾病等因素对疫苗效力有显著影响。本研究结果突出了辉瑞-生物科技公司(BNT162b2)疫苗在降低有症状COVID-19几率方面的有效性,特别是通过降低发烧、咳嗽、肌痛以及味觉或嗅觉丧失等关键症状的发生率。突破性感染仍然会发生,这表明虽然疫苗降低了症状严重程度,但可能无法完全预防感染。与之前的变体相比,这种疫苗效力较低,表明疫苗效力方面存在潜在挑战。该研究强调了持续监测以及可能需要接种加强针以增强保护的必要性,特别是针对像奥密克戎这样不断演变的变体。