Silva-Pilipich Noelia, Beloki Uxue, Salaberry Laura, Smerdou Cristian
Division of DNA and RNA Medicine, Cima Universidad de Navarra, 31008 Pamplona, Spain.
Instituto de Investigación Sanitaria de Navarra (IdISNA) and CCUN, 31008 Pamplona, Spain.
Vaccines (Basel). 2024 Mar 17;12(3):318. doi: 10.3390/vaccines12030318.
SARS-CoV-2 virus, the causative agent of COVID-19, has produced the largest pandemic in the 21st century, becoming a very serious health problem worldwide. To prevent COVID-19 disease and infection, a large number of vaccines have been developed and approved in record time, including new vaccines based on mRNA encapsulated in lipid nanoparticles. While mRNA-based vaccines have proven to be safe and effective, they are more expensive to produce compared to conventional vaccines. A special type of mRNA vaccine is based on self-amplifying RNA (saRNA) derived from the genome of RNA viruses, mainly alphaviruses. These saRNAs encode a viral replicase in addition to the antigen, usually the SARS-CoV-2 spike protein. The replicase can amplify the saRNA in transfected cells, potentially reducing the amount of RNA needed for vaccination and promoting interferon I responses that can enhance adaptive immunity. Preclinical studies with saRNA-based COVID-19 vaccines in diverse animal models have demonstrated the induction of robust protective immune responses, similar to conventional mRNA but at lower doses. Initial clinical trials have confirmed the safety and immunogenicity of saRNA-based vaccines in individuals that had previously received authorized COVID-19 vaccines. These findings have led to the recent approval of two of these vaccines by the national drug agencies of India and Japan, underscoring the promising potential of this technology.
严重急性呼吸综合征冠状病毒2(SARS-CoV-2)病毒是新冠病毒病(COVID-19)的病原体,引发了21世纪最大规模的大流行,成为全球一个非常严重的健康问题。为预防COVID-19疾病和感染,已在创纪录的时间内研发并批准了大量疫苗,包括基于脂质纳米颗粒包裹的信使核糖核酸(mRNA)的新型疫苗。虽然基于mRNA的疫苗已被证明是安全有效的,但与传统疫苗相比,其生产成本更高。一种特殊类型的mRNA疫苗基于源自RNA病毒(主要是甲病毒)基因组的自扩增RNA(saRNA)。这些saRNA除了编码抗原(通常是SARS-CoV-2刺突蛋白)外,还编码一种病毒复制酶。复制酶可在转染细胞中扩增saRNA,可能减少疫苗接种所需的RNA量,并促进可增强适应性免疫的Ⅰ型干扰素反应。在多种动物模型中对基于saRNA的COVID-19疫苗进行的临床前研究表明,该疫苗能诱导强大的保护性免疫反应,与传统mRNA疫苗相似,但所需剂量更低。初步临床试验已证实基于saRNA的疫苗在先前接种过已获批准的COVID-19疫苗的个体中的安全性和免疫原性。这些发现促使印度和日本的国家药品机构最近批准了其中两种疫苗,突显了这项技术的广阔前景。