Given the ongoing SARS-CoV-2 pandemic, identification of immunogenic targets against the coronavirus spike glycoprotein will provide crucial advances towards the development of sensitive diagnostic tools and potential vaccine candidate targets. In this study, using pools of overlapping linear B-cell peptides, we report two IgG immunodominant regions on SARS-CoV-2 spike glycoprotein that are recognised by sera from COVID-19 convalescent patients. Notably, one is specific to SARS-CoV-2, which is located in close proximity to the receptor binding domain. The other region, which is localised at the fusion peptide, could potentially function as a pan-SARS target. Functionally, antibody depletion assays demonstrate that antibodies targeting these immunodominant regions significantly alter virus neutralisation capacities. Taken together, identification and validation of these neutralising B-cell epitopes will provide insights towards the design of diagnostics and vaccine candidates against this high priority coronavirus. Characterisation of the human antibody response to SARS-CoV-2 can help the design of serological tests and vaccines. Here, the authors identify two linear epitopes in SARS-CoV-2 spike protein that elicit neutralising antibodies in several patients and could thus be useful for serology and vaccine development.
【저자키워드】 antibodies, SARS-CoV-2, viral infection, 【초록키워드】 serological test, IgG, Vaccine development, coronavirus, Vaccines, serology, antibody, SARS-CoV-2 pandemic, spike glycoprotein, diagnostic, diagnostics, Receptor binding domain, Virus neutralisation, Region, SARS-CoV-2 spike glycoprotein, neutralising antibody, sera, SARS-CoV-2 spike protein, Patient, peptides, vaccine candidate, target, B-cell epitope, targets, fusion peptide, B-cell, overlapping, human antibody response, help, immunogenic, immunodominant, Alter, linear epitope, neutralising, COVID-19 convalescent patients, identify, significantly, linear, elicit, 【제목키워드】 Spike protein, neutralising antibody, COVID-19 patient, linear epitope, elicit, the SARS-CoV-2,