Antibody evasion associated with the RBD significant mutations in several emerging SARS-CoV-2 variants and its subvariants

免疫逃逸 抗体 严重急性呼吸综合征冠状病毒2型(SARS-CoV-2) 突变 2019年冠状病毒病(COVID-19) 病毒学 生物 遗传学 基因 免疫系统 医学 疾病 病理 传染病(医学专业)
作者
Manojit Bhattacharya,Srijan Chatterjee,Sang‐Soo Lee,Kuldeep Dhama,Chiranjib Chakraborty
出处
期刊:Drug Resistance Updates [Elsevier BV]
卷期号:71: 101008-101008 被引量:5
标识
DOI:10.1016/j.drup.2023.101008
摘要

Since the origin of the wild strain of SARS-CoV-2, several variants have emerged, which were designated as VOC, VOI, and VUM from time to time. The Omicron variant is noted as the recent VOC. After the origin of the Omicron variant on November 2021, several subvariants of Omicron have originated subsequently, like BA.1/2, BA.2.75/2.75.2, BA.4/5, BF.7, BQ.1/1.1, XBB.1/1.5, etc. which are circulated throughout the globe. Scientists reported that antibody escape is a common phenomenon observed in all the previous VOCs, VOIs, including Omicron and its subvariants. The mutations in the NTD (N-terminal domain) and RBD (Receptor-binding domain) of the spike of these variants and subvariants are responsible for antibody escape. At the same time, it has been noted that spike RBD mutations have been increasing in the last few months. This review illustrates significant RBD mutations namely R346T, K417N/T, L452R, N460K E484A/K/Q, and N501Y found in the previous emerging SARS-CoV-2 variants, including Omicron and its subvariants in high frequency and their role in antibody evasion and immune evasion. The review also describes the different classes of nAb responsible for antibody escape in SARS-CoV-2 variants and the molecular perspective of the mutation in nAb escape. It will help the future researchers to develop efficient vaccines which can finally prevent the pandemic.
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