Istituto Nazionale per Le Malattie Infettive Lazzaro Spallanzani IRCCS, 00149 Rome, Italy.
ReiThera Srl, 00128 Rome, Italy.
Sci Transl Med. 2022 Jan 12;14(627):eabj1996. doi: 10.1126/scitranslmed.abj1996.
Safe and effective vaccines against coronavirus disease 2019 (COVID-19) are essential for ending the ongoing pandemic. Although impressive progress has been made with several COVID-19 vaccines already approved, it is clear that those developed so far cannot meet the global vaccine demand alone. We describe a COVID-19 vaccine based on a replication-defective gorilla adenovirus expressing the stabilized prefusion severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) spike protein named GRAd-COV2. We assessed the safety and immunogenicity of a single-dose regimen of this vaccine in healthy younger and older adults to select the appropriate dose for each age group. For this purpose, a phase 1, dose-escalation, open-labeled trial was conducted including 90 healthy participants (45 aged 18 to 55 years old and 45 aged 65 to 85 years old) who received a single intramuscular administration of GRAd-COV2 at three escalating doses. Local and systemic adverse reactions were mostly mild or moderate and of short duration, and no serious adverse events were reported. Four weeks after vaccination, seroconversion to spike protein and receptor binding domain was achieved in 43 of 44 young volunteers and in 45 of 45 older participants. Consistently, neutralizing antibodies were detected in 42 of 44 younger-age and 45 of 45 older-age volunteers. In addition, GRAd-COV2 induced a robust and T helper 1 cell (T1)–skewed T cell response against the spike protein in 89 of 90 participants from both age groups. Overall, the safety and immunogenicity data from the phase 1 trial support the further development of this vaccine.
安全有效的 2019 年冠状病毒病(COVID-19)疫苗对于结束当前大流行至关重要。尽管已经批准了几种 COVID-19 疫苗,取得了令人瞩目的进展,但显然目前开发的疫苗无法单独满足全球疫苗需求。我们描述了一种基于表达稳定的融合前严重急性呼吸综合征冠状病毒 2(SARS-CoV-2)刺突蛋白的复制缺陷型大猩猩腺病毒的 COVID-19 疫苗,该疫苗命名为 GRAd-COV2。我们评估了该疫苗在健康年轻和老年成年人中的单剂方案的安全性和免疫原性,以选择每个年龄组的适当剂量。为此,进行了一项 1 期、剂量递增、开放性标签试验,包括 90 名健康参与者(45 名年龄在 18 至 55 岁之间,45 名年龄在 65 至 85 岁之间),他们接受了三种递增剂量的 GRAd-COV2 单次肌肉内给药。局部和全身不良反应主要为轻度或中度,持续时间短,无严重不良事件报告。接种后 4 周,44 名年轻志愿者中的 43 名和 45 名老年参与者中的 45 名实现了对刺突蛋白和受体结合域的血清转化。一致地,在 44 名年轻志愿者中的 42 名和 45 名老年志愿者中的 45 名中检测到中和抗体。此外,GRAd-COV2 在 90 名来自两个年龄组的参与者中的 89 名中诱导了针对刺突蛋白的强烈且 T 辅助 1 细胞(T1)偏向的 T 细胞反应。总体而言,1 期试验的安全性和免疫原性数据支持该疫苗的进一步开发。