Saint Petersburg Scientific Research Institute of Vaccines and Serums of the Federal Medical-Biological Agency of Russia (SPbSRIVS), Saint Petersburg, Russia.
Saint Petersburg Scientific Research Institute of Vaccines and Serums of the Federal Medical-Biological Agency of Russia (SPbSRIVS), Saint Petersburg, Russia.
J Infect. 2024 Nov;89(5):106288. doi: 10.1016/j.jinf.2024.106288. Epub 2024 Sep 26.
Despite the success of first-generation COVID-19 vaccines targeting the spike (S) protein, emerging SARS-CoV-2 variants have led to immune escape, reducing the efficacy of these vaccines. Additionally, some individuals are unable to mount an effective immune response to S protein-based vaccines. This has created a need for alternative vaccine strategies that are less susceptible to mutations and capable of providing broad and durable protection. This study aimed to evaluate the efficacy and safety of a novel COVID-19 vaccine based on the full-length recombinant nucleocapsid (N) protein of SARS-CoV-2.
We conducted a prospective, multicenter, randomized, double-blind, placebo-controlled phase 3 clinical trial (NCT05726084) in Russia. Participants (n = 5229) were adults aged 18 years and older, with a BMI of 18.5-30 kg/m², and without significant clinical abnormalities. They were randomized in a 2:1 ratio to receive a single intramuscular dose of either the N protein-based vaccine (50 µg) or placebo. Randomization was done through block randomization, and masking was ensured by providing visually identical formulations of vaccine and placebo. The primary outcome was the incidence of symptomatic COVID-19 confirmed by PCR more than 15 days after vaccination within a 180-day observation period, analyzed on an intention-to-treat basis.
Between May 18, 2023, and August 9, 2023, 5229 participants were randomized, with 3486 receiving the vaccine and 1743 receiving the placebo. Eight cases of PCR-confirmed symptomatic COVID-19 occurred in the vaccine group (0.23%) compared to 27 cases in the placebo group (1.55%), yielding a vaccine efficacy of 85.2% (95% CI: 67.4-93.3; p < 0.0001). Adverse events were mostly mild and included local injection site reactions. There were no vaccine-related serious adverse events.
The N protein-based COVID-19 vaccine demonstrated significant efficacy and a favorable safety profile, suggesting it could be a valuable addition to the global vaccination effort, particularly in addressing immune escape variants and offering an alternative for those unable to respond to S protein-based vaccines. These results support the continued development and potential deployment of N protein-based vaccines in the ongoing fight against COVID-19.
尽管第一代针对刺突(S)蛋白的 COVID-19 疫苗取得了成功,但新兴的 SARS-CoV-2 变体已导致免疫逃逸,降低了这些疫苗的效力。此外,一些人无法对基于 S 蛋白的疫苗产生有效的免疫反应。这就需要开发替代疫苗策略,这些策略不易发生突变,并能提供广泛和持久的保护。本研究旨在评估一种新型 COVID-19 疫苗的疗效和安全性,该疫苗基于 SARS-CoV-2 的全长重组核衣壳(N)蛋白。
我们在俄罗斯进行了一项前瞻性、多中心、随机、双盲、安慰剂对照的 3 期临床试验(NCT05726084)。参与者(n=5229)为年龄在 18 岁及以上、BMI 为 18.5-30kg/m²且无明显临床异常的成年人。他们以 2:1 的比例随机接受单次肌肉内剂量的 N 蛋白疫苗(50μg)或安慰剂。通过区组随机化进行随机分组,通过提供外观相同的疫苗和安慰剂制剂来确保盲法。主要结局是在 180 天观察期内,接种后 15 天以上通过 PCR 确认的有症状 COVID-19 的发生率,基于意向治疗进行分析。
2023 年 5 月 18 日至 8 月 9 日,5229 名参与者被随机分组,其中 3486 名接受疫苗,1743 名接受安慰剂。疫苗组发生 8 例 PCR 确诊的有症状 COVID-19 病例(0.23%),安慰剂组发生 27 例(1.55%),疫苗效力为 85.2%(95%CI:67.4-93.3;p<0.0001)。不良事件大多为轻度,包括局部注射部位反应。无疫苗相关严重不良事件。
N 蛋白 COVID-19 疫苗显示出显著的疗效和良好的安全性,表明它可能是全球疫苗接种工作的一项有价值的补充,特别是在应对免疫逃逸变体方面,并为无法对基于 S 蛋白的疫苗产生反应的人群提供了一种替代方案。这些结果支持继续开发和潜在部署 N 蛋白疫苗,以应对持续的 COVID-19 疫情。