Strategies and Challenges in the Development of Coronavirus Disease-2019 Vaccine

Pratibha Gupta
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Abstract

The novel coronavirus infection (coronavirus disease-2019 (COVID-19)) emerged from Wuhan in the Hubei Province of China in late 2019. Millions of people were infected with COVID-19 pandemic due to the long incubation period of the virus inside the human body and the dearth of available treatments or vaccines. High transmission rates created havoc, which highlighted the urgent need for effective interventions to stop the spread and clinical impact of the virus on patients and populations. Previous research on severe acute respiratory syndrome coronavirus (SARS-CoV) provides information on vaccination strategies that could inform how governments approach the elimination of this novel coronavirus. Numerous efforts have been made to develop vaccines against Middle East respiratory syndrome (MERS) and SARS. The spike glycoprotein or S protein is the critical target for most of the drugs and vaccines against coronavirus. The virus uses the spike (S) protein for entering the host cell, by interacting with the receptor called angiotensin converting enzyme-2 (ACE2). Various vaccine platforms are available such as nucleic acid vaccine, protein-based vaccines, virus-vectored vaccines and live or attenuated vaccines, with each having their advantages and disadvantages. This review focuses on the overview of different vaccine candidates used, those currently in development, and the challenges encountered while developing effective vaccines.
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冠状病毒病-2019疫苗研制的策略与挑战
新型冠状病毒感染(冠状病毒病-2019 (COVID-19))于2019年底在中国湖北省武汉市出现。由于病毒在人体内潜伏期长,缺乏可用的治疗或疫苗,数百万人感染了COVID-19大流行。高传播率造成了严重破坏,这突出表明迫切需要采取有效干预措施,以阻止病毒的传播和对患者和人群的临床影响。以前对严重急性呼吸综合征冠状病毒(SARS-CoV)的研究提供了有关疫苗接种策略的信息,可以为各国政府如何消除这种新型冠状病毒提供信息。为研制对抗中东呼吸综合征和非典型肺炎的疫苗作出了大量努力。刺突糖蛋白或S蛋白是大多数抗冠状病毒药物和疫苗的关键靶点。病毒利用刺突蛋白(S)进入宿主细胞,通过与受体血管紧张素转换酶-2 (ACE2)相互作用。核酸疫苗、蛋白疫苗、病毒载体疫苗、活疫苗或减毒疫苗等疫苗平台多种多样,各有优缺点。本综述的重点是概述使用的不同候选疫苗、目前正在开发的候选疫苗以及开发有效疫苗时遇到的挑战。
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