Safety, tolerability, and immunogenicity of a recombinant adenovirus type-5 vectored COVID-19 vaccine: a dose-escalation, open-label, non-randomised, first-in-human trial

2020 The Lancet 1,434 citations

Abstract

A vaccine to protect against COVID-19 is urgently needed. We aimed to assess the safety, tolerability, and immunogenicity of a recombinant adenovirus type-5 (Ad5) vectored COVID-19 vaccine expressing the spike glycoprotein of a severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) strain. Between March 16 and March 27, 2020, we screened 195 individuals for eligibility. Of them, 108 participants (51% male, 49% female; mean age 36·3 years) were recruited and received the low dose (n=36), middle dose (n=36), or high dose (n=36) of the vaccine. All enrolled participants were included in the analysis. At least one adverse reaction within the first 7 days after the vaccination was reported in 30 (83%) participants in the low dose group, 30 (83%) participants in the middle dose group, and 27 (75%) participants in the high dose group. The most common injection site adverse reaction was pain, which was reported in 58 (54%) vaccine recipients, and the most commonly reported systematic adverse reactions were fever (50 [46%]), fatigue (47 [44%]), headache (42 [39%]), and muscle pain (18 [17%]. Most adverse reactions that were reported in all dose groups were mild or moderate in severity. No serious adverse event was noted within 28 days post-vaccination. ELISA antibodies and neutralising antibodies increased significantly at day 14, and peaked 28 days post-vaccination. Specific T-cell response peaked at day 14 post-vaccination. The Ad5 vectored COVID-19 vaccine is tolerable and immunogenic at 28 days post-vaccination. Humoral responses against SARS-CoV-2 peaked at day 28 post-vaccination in healthy adults, and rapid specific T-cell responses were noted from day 14 post-vaccination. Our findings suggest that the Ad5 vectored COVID-19 vaccine warrants further investigation. National Key R&D Program of China, National Science and Technology Major Project, and CanSino Biologics.

Keywords

MedicineTolerabilityImmunogenicityAdverse effectVaccinationVirologyImmunologyInternal medicineAntibody

MeSH Terms

AdenoviridaeAdolescentAdultAntibodiesNeutralizingAntibodiesViralBetacoronavirusCOVID-19COVID-19 VaccinesChinaCoronavirus InfectionsEnzyme-Linked Immunosorbent AssayFemaleHumansImmunityCellularImmunityHumoralInjectionsIntramuscularMaleMiddle AgedPandemicsPneumoniaViralSARS-CoV-2T-LymphocytesVaccinesSyntheticViral VaccinesYoung Adult

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Publication Info

Year
2020
Type
article
Volume
395
Issue
10240
Pages
1845-1854
Citations
1434
Access
Closed

Citation Metrics

1434
OpenAlex
39
Influential
1140
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Cite This

Fengcai Zhu, Yu-Hua Li, Xu-Hua Guan et al. (2020). Safety, tolerability, and immunogenicity of a recombinant adenovirus type-5 vectored COVID-19 vaccine: a dose-escalation, open-label, non-randomised, first-in-human trial. The Lancet , 395 (10240) , 1845-1854. https://doi.org/10.1016/s0140-6736(20)31208-3

Identifiers

DOI
10.1016/s0140-6736(20)31208-3
PMID
32450106
PMCID
PMC7255193

Data Quality

Data completeness: 86%