Sampson Alexander T, Hlaváč Matěj, Gillman Adam C T, Douradinha Bruno, Gilbert Sarah C
Pandemic Sciences Institute, Nuffield Department of Medicine, University of Oxford, Oxford, UK.
Oxford Vaccine Group, Department of Paediatrics, University of Oxford, Oxford, UK.
Hum Vaccin Immunother. 2025 Dec;21(1):2514356. doi: 10.1080/21645515.2025.2514356. Epub 2025 Jul 1.
The COVID-19 pandemic saw the first extensive use of adenoviral vector vaccines, with over 3 billion doses produced during the first year of the pandemic alone and an estimated 6 million lives saved. These vaccines were safe and effective, and could be produced at low cost in several continents allowing widespread use in low- and middle-income countries (LMICs). Despite their successful deployment against SARS-CoV-2, their impact has been overshadowed by relatively lower immunogenicity in contrast to mRNA vaccine technologies and very rare but serious adverse events such as vaccine-induced thrombotic thrombocytopaenia (VITT). The next-generation of adenoviral vector vaccines must address these challenges: here, we explore strategies to improve immunogenicity and safety by novel serotype selection, vector engineering, capsid modification and new delivery technologies, and discuss opportunities for next-generation adenoviral vectors against infectious disease and cancer.
在新冠疫情期间,腺病毒载体疫苗首次得到广泛使用,仅在疫情的第一年就生产了超过30亿剂,估计拯救了600万人的生命。这些疫苗安全有效,并且可以在多个大洲以低成本生产,从而得以在低收入和中等收入国家广泛使用。尽管它们在对抗新冠病毒方面成功部署,但与mRNA疫苗技术相比,其免疫原性相对较低,以及非常罕见但严重的不良事件,如疫苗诱导的血栓性血小板减少症(VITT),使其影响有所逊色。下一代腺病毒载体疫苗必须应对这些挑战:在此,我们探索通过新型血清型选择、载体工程、衣壳修饰和新的递送技术来提高免疫原性和安全性的策略,并讨论下一代腺病毒载体在对抗传染病和癌症方面的机遇。