Etiologically Elusive Disorders Research Network (EEDRN), New Delhi, India.
Department of Anatomy, All India Institute of Medical Sciences (AIIMS), Patna, India.
J Med Virol. 2022 Apr;94(4):1300-1314. doi: 10.1002/jmv.27467. Epub 2021 Nov 29.
Young age, female sex, absence of comorbidities, and prior infection or vaccination are known epidemiological barriers for contracting the new infection and/or increased disease severity. Demographic trends from the recent coronavirus disease 2019 waves, which are believed to be driven by newer severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) variants, indicate that the aforementioned epidemiological barriers are being breached and a larger number of younger and healthy individuals are developing severe disease. The new SARS-CoV-2 variants have key mutations that can induce significant changes in the virus-host interactions. Recent studies report that, some of these mutations, singly or in a group, enhance key mechanisms, such as binding of the receptor-binding domain (RBD) of the viral spike protein with the angiotensin-converting enzyme 2 (ACE2) receptor in the host-cells, increase the glycosylation of spike protein at the antigenic sites, and enhance the proteolytic cleavage of the spike protein, thus leading to improved host-cell entry and the replication of the virus. The putative changes in the virus-host interactions imparted by the mutations in the RBD sequence can potentially be the reason behind the breach of the observed epidemiological barriers. Susceptibility for contracting SARS-CoV-2 infection and the disease outcomes are known to be influenced by host-cell expressions of ACE2 and other proteases. The new variants can act more efficiently, and even with the lesser availability of the viral entry-receptor and the associated proteases, can have more efficient host-cell entry and greater replication resulting in high viral loads and prolonged viral shedding, widespread tissue-injury, and severe inflammation leading to increased transmissibility and lethality. Furthermore, the accumulating evidence shows that multiple new variants have reduced neutralization by both, natural and vaccine-acquired antibodies, indicating that repeated and vaccine breakthrough infections may arise as serious health concerns in the ongoing pandemic.
年龄较小、女性、无合并症以及既往感染或接种疫苗,这些都是感染新病毒和/或加重疾病严重程度的已知流行病学障碍。最近的 2019 年冠状病毒病(COVID-19)浪潮的人口统计学趋势表明,上述流行病学障碍正在被突破,越来越多的年轻和健康个体出现严重疾病,这被认为是由新型严重急性呼吸综合征冠状病毒 2(SARS-CoV-2)变异株引起的。新型 SARS-CoV-2 变异株具有关键突变,这些突变可导致病毒-宿主相互作用发生重大变化。最近的研究报告称,其中一些突变,无论是单一突变还是一组突变,都可增强关键机制,如病毒刺突蛋白的受体结合域(RBD)与宿主细胞中的血管紧张素转化酶 2(ACE2)受体的结合、增加抗原位点上的刺突蛋白糖基化,以及增强刺突蛋白的蛋白水解切割,从而导致宿主细胞进入和病毒复制能力增强。RBD 序列突变引起的病毒-宿主相互作用的假定变化可能是观察到的流行病学障碍被突破的原因。感染 SARS-CoV-2 的易感性和疾病结局已知受 ACE2 和其他蛋白酶在宿主细胞中的表达影响。新型变异株可能更有效地发挥作用,即使病毒进入受体和相关蛋白酶的可用性较低,也能更有效地进入宿主细胞并进行大量复制,导致高病毒载量和延长的病毒脱落,广泛的组织损伤和严重的炎症,从而增加传染性和致死性。此外,越来越多的证据表明,多种新型变异株对自然和疫苗获得的抗体的中和作用降低,这表明在持续的大流行中,反复感染和疫苗突破性感染可能成为严重的健康问题。