Relating the SARS-CoV-2 Spike Protein to Infectivity, Pathogenicity, and Immunogenicity in COVID-19

N. V
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Abstract

Introduction: SARS-CoV-2 Life Cycle: The disease which reportedly began in Chinese city Wuhan in November-December 2019 manifesting as severe respiratory illness, soon spread to various parts of the world, and was named COVID-19, and declared a pandemic by WHO. The life cycle of SARS-CoV-2 begins with membrane fusion mediated by Spike (S) protein binding to the ACE2 receptors. Following viral entry and release of genome into the host cell cytoplasm there occurs replication and transcription to generate viral structural and non-structural proteins. Finally, VLPs are produced and the mature virions are released from the host cell. Immunogenicity of the Spike Protein: The S protein is considered the main antigenic component among structural proteins of SARS-CoV-2 and responsible for inducing the host immune response. The neutralising antibodies (nAbs) targeting the S protein are produced and may confer a protective immunity against the viral infection. Further, the role of the S protein in infectivity also makes it an important tool for diagnostic antigen-based testing and vaccine development. The S-specific antibodies, memory B and circulating TFH cells are consistently elicited following SARS-CoV-2 infection, and COVID-19 vaccine shots in clinical trials. The Emerging SARS-CoV-2 Variants: The early genomic variations in SARS-CoV-2 have gone almost unnoticed having lacked an impact on disease transmission or its clinical course. Some of the recently discovered mutations, however, have impact on transmissibility, infectivity, or immune response. One such mutation is the D614G variant, which has increased in prevalence to currently become the dominant variant world-over. Another, relatively new variant, named VUI-202012/01 or B.1.1.7 has acquired 17 genomic alterations and carries the risk of enhanced infectivity. Further, its potential impact on vaccine efficacy is a worrisome issue. Conclusion: The Unmet Challenges: COVID-19 as a disease and SARS-CoV-2 as its causative organism, continue to remain an enigma. While we continue to explore the agent factors, disease transmission dynamics, pathogenesis and clinical spectrum of the disease, and therapeutic modalities, the grievous nature of the disease has led to emergency authorizations for COVID-19 vaccines in various countries. Further, the virus may continue to persist and afflict for years to come, as future course of the disease is linked to certain unknown factors like effects of seasonality on virus transmission and unpredictable nature of immune response to the disease.
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SARS-CoV-2刺突蛋白与COVID-19传染性、致病性和免疫原性的关系
SARS-CoV-2生命周期:据报道,该疾病于2019年11月至12月在中国武汉市开始,表现为严重的呼吸道疾病,很快传播到世界各地,并被命名为COVID-19,并被世卫组织宣布为大流行。SARS-CoV-2的生命周期始于Spike (S)蛋白与ACE2受体结合介导的膜融合。病毒进入并释放基因组进入宿主细胞质后,发生复制和转录,生成病毒结构蛋白和非结构蛋白。最后,产生VLPs,成熟病毒粒子从宿主细胞中释放出来。刺突蛋白的免疫原性:S蛋白被认为是SARS-CoV-2结构蛋白中的主要抗原成分,负责诱导宿主免疫反应。产生针对S蛋白的中和抗体(nab),并可能赋予对病毒感染的保护性免疫。此外,S蛋白在感染性中的作用也使其成为基于抗原的诊断测试和疫苗开发的重要工具。在临床试验中,s特异性抗体、记忆B和循环TFH细胞在SARS-CoV-2感染和COVID-19疫苗接种后一致被激发。新出现的SARS-CoV-2变异:SARS-CoV-2的早期基因组变异几乎没有被注意到,对疾病传播或其临床过程没有影响。然而,最近发现的一些突变对传播性、传染性或免疫反应有影响。其中一种突变是D614G变异,它的流行率越来越高,目前已成为世界范围内的主要变异。另一种相对较新的变异,名为VUI-202012/01或B.1.1.7,获得了17个基因组改变,具有增强传染性的风险。此外,它对疫苗效力的潜在影响是一个令人担忧的问题。结论:未解决的挑战:COVID-19作为一种疾病,SARS-CoV-2作为其致病生物,仍然是一个谜。在我们继续探索病原体因素、疾病传播动态、疾病发病机制和临床谱以及治疗方式的同时,该疾病的严重性质已导致各国紧急批准COVID-19疫苗。此外,这种病毒可能会持续存在并在未来几年肆虐,因为这种疾病的未来进程与某些未知因素有关,比如病毒传播的季节性影响,以及对这种疾病的免疫反应的不可预测性。
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