Effectiveness of a booster dose of aerosolized or intramuscular adenovirus type 5 vectored COVID-19 vaccine in adults with hybrid immunity against COVID-19: a multicenter, partially randomized, platform trial in China

Siyue Jia, Yuanbao Liu, Qian He, Hongxing Pan, Zhenglun Liang, Juan Zhou, Yingzi Pan, Sheng Liu, Jingjing Wu, Kun Yang, Xuanxuan Zhang, Yang Zhao, Simin Li, Lei Zhang, Li Chen, Aihua Yao, Mengyi Lu, Qunying Mao, Fengcai Zhu, Jingxin Li
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Abstract

Background The primary objective of this research was to assess if a booster dose with COVID-19 vaccines containing ancestral strain could still provide significant protection against symptomatic SARS-CoV-2 infection in a predominantly hybrid-immune population during the period of omicron variant dominance. Methods We did a multicenter, partially randomized, platform trial to evaluate the effectiveness of a booster dose of an aerosolized or intramuscular adenovirus type 5 vectored COVID-19 vaccine (Ad5-nCoV) in adults, after the national-wide omicron circulating at the end of year 2022 in China. Participants who were willing to receive a COVID-19 booster dose were randomly assigned to receive one of the booster doses. While, those participants who refused to take a booster dose but consented to participate COVID-19 surveillance were included in a control group. Both participants receiving a booster dose or not were monitored for symptomatic COVID-19 during a six-month surveillance period. Results Between May 23, 2023, and August 28, 2023, 4089 eligible participants were equally randomized to receive a booster dose of aerosolized Ad5-nCoV through oral inhalation at 0.1mL (IH Ad5-nCoV, n=2039) or intramuscular injection of Ad5-nCoV at 0.5 mL (IM Ad5-nCoV, n=2050). While, 2008 participants were enrolled in the blank-control group. A total of 79 COVID-19 cases were confirmed, with 22 (0.006%) in the IH Ad5-nCoV group, 23 (0.007%) in the IM Ad5-nCoV group, and 34 (0.01%) in the control group. Adjusted effectiveness of IH Ad5-nCoV and IM Ad5-nCoV from 14 days after the vaccination were 51.6% (95% CI 9.0 to 74.3) and 38.1% (95% CI -9.6 to 65.1), respectively. Interpretation Significant protection against symptomatic COVID-19 caused by the Omicron variant, during the ongoing pandemic of evolving COVID-19 variants, was found to be provided by boosting with the ancestral strain-containing vaccine IH Ad5-nCoV, but not by boosting with IM Ad5-nCoV.
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COVID-19混合免疫成人接种气雾或肌肉注射5型腺病毒载体COVID-19疫苗的效果:中国多中心、部分随机、平台试验
背景 本研究的主要目的是评估在奥米克变异株占优势的时期,使用含有祖先株的 COVID-19 疫苗加强剂量是否仍能为以混合免疫为主的人群提供显著的保护,使其免受无症状的 SARS-CoV-2 感染。方法 我们进行了一项多中心、部分随机、平台试验,以评估在中国 2022 年底全国范围内流行 Omicron 之后,成人接种气雾或肌肉注射 5 型腺病毒载体 COVID-19 疫苗(Ad5-nCoV)的效果。愿意接种COVID-19强化剂的参与者被随机分配接种其中一剂强化剂。而拒绝接受加强剂但同意参与COVID-19监测的参与者则被纳入对照组。在为期 6 个月的监测期间,对接受或未接受加强剂量的参与者都进行了 COVID-19 症状监测。结果 在2023年5月23日至2023年8月28日期间,4089名符合条件的参与者被平均随机分配到通过口腔吸入0.1毫升气雾化Ad5-nCoV(IH Ad5-nCoV,n=2039)或肌肉注射0.5毫升Ad5-nCoV(IM Ad5-nCoV,n=2050)接受加强剂量。空白对照组有 2008 名参与者。共有79例COVID-19确诊,其中IH Ad5-nCoV组22例(0.006%),IM Ad5-nCoV组23例(0.007%),对照组34例(0.01%)。接种后 14 天,IH Ad5-nCoV 和 IM Ad5-nCoV 的调整有效率分别为 51.6%(95% CI 9.0 至 74.3)和 38.1%(95% CI -9.6 至 65.1)。释义 在COVID-19变异株不断演变的大流行期间,接种含祖先毒株的疫苗IH Ad5-nCoV可对由Omicron变异株引起的症状性COVID-19提供显著保护,而接种IM Ad5-nCoV则不能。
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