Jia Siyue, Shao Chengwei, Cheng Xin, Pan Hongxing, Wang Zhijian, Xia Yu, Xu Jianfang, Huai Xuefen, Leng Danjing, Wang Jiarong, Zhao Gan, Wang Bin, Li Jingxin, Zhu Fengcai
Jiangsu Provincial Medical Innovation Center, National Health Commission Key Laboratory of Enteric Pathogenic Microbiology, Jiangsu Provincial Center for Disease Control and Prevention (Jiangsu Provincial Academy of Preventive Medicine), Nanjing, China.
School of Public Health, Southeast University, Nanjing, China.
Hum Vaccin Immunother. 2025 Dec;21(1):2448405. doi: 10.1080/21645515.2024.2448405. Epub 2025 Jan 26.
INO-4800 represents a DNA-based vaccine encoding the spike protein of SARS-CoV-2. This phase 2 trial evaluated the immunogenicity and safety of INO-4800 as a primary vaccination series in adults. We conducted a randomized, observer-blind, placebo-controlled phase 2 trial of intradermal injection of INO-4800 in both healthy adults and elderly individuals. Eligible participants from each age group were enrolled and randomly assigned in a 3:3:2 ratio to receive two doses of INO-4800 (1.0 mg or 2.0 mg) or placebo, followed by electroporation on day 0 and day 28. The primary immunogenicity endpoints focused on determining the geometric mean titers (GMTs) of spike-binding antibodies and live SARS-CoV-2 neutralizing antibody at day 30 after the second dose. The primary endpoint for safety was the occurrence of adverse events within 30 days after vaccination. A total of 781 volunteers were recruited and screened for eligibility, with 320 eligible young adults (≥18 to <60 years old) and 320 elderly (≥60 to ≤85 years old) were randomly assigned to receive the low-dose (1.0 mg, = 120) or high-dose (2.0 mg, = 120) INO-4800, or placebo ( = 80). Notably, both dose groups exhibited significant increases in spike-binding antibodies at day 30 after the second dose, with GMTs of 1609.3 (95% CI: 1385.5-1869.3) for the low-dose group and 3016.7 (95% CI: 2577.4-3530.8) for the high-dose group. Additionally, both dose groups induced neutralizing antibodies against live SARS-CoV-2, with GMTs of 4.7 (95% CI: 4.2-5.3) and 6.6 (95% CI: 5.9-7.4) at day 30 after the second dose. The incidence of adverse events within 30 days after vaccination was slightly higher in the high-dose group (115 [47.9%]) than that in the low-dose group (105 [43.8%]) ( = .0060). All adverse reactions were grade 1 or 2, primarily occurring within 14 days after vaccination. No vaccine-related serious adverse events were reported. The COVID-19 DNA vaccine INO-4800 at two doses (1.0 mg or 2.0 mg) showed an acceptable safety profile and modest immunogenicity, with the high-dose slightly more immunogenic than the low-dose. www.chictr.org.cn, identifier is ChiCTR2000040146.
INO-4800是一种基于DNA的疫苗,编码严重急性呼吸综合征冠状病毒2(SARS-CoV-2)的刺突蛋白。该2期试验评估了INO-4800作为成人初次疫苗接种系列的免疫原性和安全性。我们在健康成年人和老年人中进行了一项皮内注射INO-4800的随机、观察者盲法、安慰剂对照2期试验。每个年龄组符合条件的参与者被招募,并按3:3:2的比例随机分配,接受两剂INO-4800(1.0毫克或2.0毫克)或安慰剂,然后在第0天和第28天进行电穿孔。主要免疫原性终点集中在确定第二剂后第30天刺突结合抗体和活SARS-CoV-2中和抗体的几何平均滴度(GMT)。安全性的主要终点是接种疫苗后30天内不良事件的发生情况。共招募并筛选了781名志愿者以确定其是否符合条件,320名符合条件的年轻成年人(≥18至<60岁)和320名老年人(≥60至≤85岁)被随机分配接受低剂量(1.0毫克,n = 120)或高剂量(2.0毫克,n = 120)INO-4800,或安慰剂(n = 80)。值得注意的是,两个剂量组在第二剂后第30天刺突结合抗体均显著增加,低剂量组的GMT为1609.3(95%置信区间:1385.5 - 1869.3),高剂量组为3016.7(95%置信区间:2577.4 - 3530.8)。此外,两个剂量组均诱导出针对活SARS-CoV-2的中和抗体,第二剂后第30天的GMT分别为4.7(95%置信区间:4.2 - 5.3)和6.6(95%置信区间:5.9 - 7.4)。接种疫苗后30天内不良事件的发生率在高剂量组(115 [47.9%])略高于低剂量组(105 [43.8%])(P = 0.0060)。所有不良反应均为1级或2级,主要发生在接种疫苗后的14天内。未报告与疫苗相关的严重不良事件。两剂(1.0毫克或2.0毫克)的新型冠状病毒病DNA疫苗INO-4800显示出可接受的安全性和适度的免疫原性,高剂量组的免疫原性略高于低剂量组。中国临床试验注册中心,标识符为ChiCTR2000040146。