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虫媒正黄病毒mRNA疫苗研究进展

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虫媒正黄病毒种类多、传播快、致病强,长期严重威胁公共卫生安全,目前仍然缺乏针对正黄病毒的特异性治疗手段.疫苗接种是防控正黄病毒传播和感染的重要手段,多种制备技术生产的传统疫苗在黄热病毒、日本发脑炎病毒、森林脑炎病毒和登革病毒的防控中发挥了关键性作用.然而,这些疫苗在安全性和免疫效力上仍有待进一步提高和完善.值得注意的是,在新型冠状病毒大流行的背景下,可快速制备的mRNA疫苗成为了应对新突发传染病的关键疫苗技术,必将极大地助力快速研发安全、高效的正黄病毒疫苗,为未来正黄病毒的科学防控奠定基础.为此,本文首先对mRNA疫苗的分子基础和作用机制进行了总结.然后,着重介绍了几种正黄病毒的生物学特征和流行情况,以及针对这些病毒的mRNA疫苗研究现状.最后,对合成生物学、核苷酸修饰技术和新型递送系统在未来mRNA疫苗研发中的作用进行了归纳,以期为未来快速研发高效、安全的正黄病毒mRNA疫苗提供研究思路和技术指导.
mRNA vaccines against arthropod-borne orthofaviviruses
Arthropod-borne orthoflaviviruses,a group of single-stranded,positive-sense RNA viruses,are primarily transmitted to humans through the bites of mosquitoes or ticks.These viruses are significant human and veterinary pathogens,capable of causing severe and widespread diseases,including encephalitis,microcephaly,hepatitis,and arthritis.Orthoflaviviruses predominantly affect tropical and subtropical regions,putting over 3 billion individuals at risk of outbreaks.Historically,conventional vaccines,such as live attenuated and inactivated vaccines,have provided durable protection against various orthoflaviviruses,including yellow fever virus,tick-borne encephalitis virus,Japanese encephalitis virus,and dengue virus.These vaccines are critical tools for preventing millions of illnesses and saving numerous lives annually.However,the safety profiles and immunogenicities of these existing vaccines require ongoing enhancement and refinement.The advent of mRNA vaccines represents a promising alternative to conventional vaccines.mRNA vaccines utilize messenger RNA(mRNA)to instruct the body to produce virus-specific proteins.These proteins can mimic those of the virus,triggering the immune system to produce viral specific B cell and T cell responses capable of combating the real virus upon exposure.Over the past decade,major technological innovations and research investments have enabled mRNA vaccines to emerge as powerful immune efficacy compared to conventional vaccines.Importantly,they can offer several advantages over conventional vaccines,including high potency,proven safety and efficacy,rapid clinical development,and cost-effective manufacturing potential.These benefits make mRNA vaccines a significant tool in accelerating the development of safe and potent vaccines against emerging and re-emerging infectious diseases.Notably,during the SARS-CoV-2 pandemic,the mRNA-1273 vaccine developed by Moderna and the BNT162b mRNA vaccines developed by Pfizer/BioNTech received approval from the US Food and Drug Administration.Additionally,many mRNA vaccines targeting multiple infectious diseases have entered clinical trials.Consequently,mRNA vaccines will undoubtedly play a pivotal role in the rapid development of safe and effective orthofavivirus vaccines.Their ability to be rapidly designed and manufactured allows for a swift response to outbreaks and the emergence of new orthofavivirus strains.In this review,we initially summarize the molecular basis and mechanism of action of mRNA vaccines,including their structure,function,in vivo replication,and translation processes.Subsequently,we briefly introduce the biological characteristics of several important orthofaviviruses,including their genome,structures,life cycle,disease symptoms and epidemic trends.Furthermore,we focus on the current status of mRNA vaccines against these viruses,covering the selected antigens,mRNA technologies,immunization methods,subject populations,and the efficacies of various mRNA vaccines.Finally,we emphasize the roles of synthetic biology,nucleotide modification technologies and novel delivery systems in the development of mRNA vaccines.In conclusion,this review offers innovative research perspectives and technical insights to accelerate the development of efficient,safe and widely accessible mRNA vaccines for orthofaviruses in the future.

arthropod-borne orthofavivirusesmRNA vaccinehumoral immunitycellular immunity

王族馨、迟航、邓永强、韩晓东

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内蒙古农业大学生命科学学院,呼和浩特 010011

中国人民解放军军事科学院军事医学研究院微生物流行病研究所,病原微生物生物安全国家重点实验室,北京 100071

虫媒正黄病毒 mRNA疫苗 体液免疫 细胞免疫

2024

科学通报
中国科学院国家自然科学基金委员会

科学通报

CSTPCD北大核心
影响因子:1.269
ISSN:0023-074X
年,卷(期):2024.69(33)