免疫系统
病毒学
病毒载体
佐剂
接种疫苗
免疫学
dna疫苗
冠状病毒
遗传增强
生物
医学
免疫
传染病(医学专业)
疾病
基因
2019年冠状病毒病(COVID-19)
重组DNA
病理
生物化学
作者
Atıl Bişgin,Ahter Dilşad Şanlioğlu,Yunus Emre Ekşi,Thomas S. Griffith,Salih Şanlıoğlu
出处
期刊:Human Gene Therapy
[Mary Ann Liebert]
日期:2021-04-16
卷期号:32 (11-12): 541-562
被引量:12
摘要
Severe acute respiratory syndrome (SARS) is a newly emerging infectious disease (COVID-19) caused by the novel coronavirus SARS-coronavirus 2 (CoV-2). To combat the devastating spread of SARS-CoV-2, extraordinary efforts from numerous laboratories have focused on the development of effective and safe vaccines. Traditional live-attenuated or inactivated viral vaccines are not recommended for immunocompromised patients as the attenuated virus can still cause disease via phenotypic or genotypic reversion. Subunit vaccines require repeated dosing and adjuvant use to be effective, and DNA vaccines exhibit lower immune responses. mRNA vaccines can be highly unstable under physiological conditions. On the contrary, naturally antigenic viral vectors with well-characterized structure and safety profile serve as among the most effective gene carriers to provoke immune response via heterologous gene transfer. Viral vector-based vaccines induce both an effective cellular immune response and a humoral immune response owing to their natural adjuvant properties via transduction of immune cells. Consequently, viral vectored vaccines carrying the SARS-CoV-2 spike protein have recently been generated and successfully used to activate cytotoxic T cells and develop a neutralizing antibody response. Recent progress in SARS-CoV-2 vaccines, with an emphasis on gene therapy viral vector-based vaccine development, is discussed in this review.
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