Providence Therapeutics Holdings, 8832 Blackfoot Trail SE, Ste 120, Calgary, AB, T2J 3J1, Canada.
Centricity Research, 2291 Kipling Avenue, Unit 117B, Toronto, ON, M9W 4L6, Canada.
Sci Rep. 2023 May 26;13(1):8557. doi: 10.1038/s41598-023-35662-y.
Access to vaccines against SARS-CoV-2 virus was limited in poor countries during the COVID-19 pandemic. Therefore, a low-cost mRNA vaccine, PTX-COVID19-B, was produced and evaluated in a Phase 1 trial. PTX-COVID19-B encodes Spike protein D614G variant without the proline-proline (986-987) mutation present in other COVID-19 vaccines. The aim of the study was to evaluate safety, tolerability, and immunogenicity of PTX-COVID19-B vaccine in healthy seronegative adults 18-64 years old. The trial design was observer-blinded, randomized, placebo-controlled, and tested ascending doses of 16-µg, 40-µg, or 100-µg in a total of 60 subjects who received two intramuscular doses, 4 weeks apart. Participants were monitored for solicited and unsolicited adverse events after vaccination and were provided with a Diary Card and thermometer to report any reactogenicity during the trial. Blood samples were collected on baseline, days 8, 28, 42, 90, and 180 for serum analysis of total IgG anti-receptor binding domain (RBD)/Spike titers by ELISA, and neutralizing antibody titers by pseudovirus assay. Titers in BAU/mL were reported as geometric mean and 95% CI per cohort. After vaccination, few solicited adverse events were observed and were mild to moderate and self-resolved within 48 h. The most common solicited local and systemic adverse event was pain at the injection site, and headache, respectively. Seroconversion was observed in all vaccinated participants, who showed high antibody titers against RBD, Spike, and neutralizing activity against the Wuhan strain. Neutralizing antibody titers were also detected against Alpha, Beta, and Delta variants of concerns in a dose dependent manner. All tested doses of PTX-COVID19-B were safe, well-tolerated, and provided a strong immunogenicity response. The 40-µg dose showed fewer adverse reactions than the 100-µg dose, and therefore was selected for a Phase 2 trial, which is currently ongoing.Clinical Trial Registration number: NCT04765436 (21/02/2021). ( https://clinicaltrials.gov/ct2/show/NCT04765436 ).
在 COVID-19 大流行期间,贫穷国家获得 SARS-CoV-2 病毒疫苗的机会有限。因此,生产了一种低成本的 mRNA 疫苗 PTX-COVID19-B,并在 I 期临床试验中进行了评估。PTX-COVID19-B 编码 Spike 蛋白 D614G 变体,而没有其他 COVID-19 疫苗中存在的脯氨酸-脯氨酸(986-987)突变。该研究的目的是评估健康血清阴性成年人 18-64 岁人群中 PTX-COVID19-B 疫苗的安全性、耐受性和免疫原性。试验设计为观察者盲法、随机、安慰剂对照,并在总共 60 名接受两次肌肉内注射、间隔 4 周的受试者中测试了 16-µg、40-µg 或 100-µg 的递增剂量。接种疫苗后,对受试者进行了征集和未征集不良事件的监测,并为他们提供了一份日记卡和温度计,以报告试验期间的任何反应性。在基线、第 8 天、第 28 天、第 42 天、第 90 天和第 180 天收集血液样本,通过 ELISA 检测血清总 IgG 抗受体结合域(RBD)/Spike 滴度,通过假病毒测定检测中和抗体滴度。BAU/mL 报告的滴度为每个队列的几何平均值和 95%CI。接种疫苗后,观察到少数征集不良事件,为轻度至中度,在 48 小时内自行缓解。最常见的征集局部和全身不良事件分别是注射部位疼痛和头痛。所有接种疫苗的参与者均发生血清转化,表现出针对 RBD、Spike 和针对武汉株的中和活性的高抗体滴度。中和抗体滴度也以剂量依赖性方式针对关注的 Alpha、Beta 和 Delta 变体进行了检测。PTX-COVID19-B 的所有测试剂量均安全且耐受良好,并提供了强烈的免疫原性反应。40-µg 剂量的不良反应比 100-µg 剂量少,因此被选为 II 期临床试验,目前正在进行中。临床试验注册号:NCT04765436(2021 年 2 月 21 日)。(https://clinicaltrials.gov/ct2/show/NCT04765436)。