Abstract
The global pandemic of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) has resulted in the generation of variants that may diminish host immune responses to vaccine formulations. Here we show a registered observational clinical trial ( NCT04795414 ), we assess the safety and immunogenicity of the inactivated SARS-CoV-2 vaccine BBIBP-CorV in a cohort of 1006 vaccine recipients. No serious adverse events are observed during the term of the study. Detectable virus-specific antibody is measured and determined to be neutralizing in 698/760 (91.84%) vaccine recipients on day 28 post second vaccine dose and in 220/581 (37.87%) vaccine recipients on day 180 post second vaccine dose, whereas vaccine-elicited sera show varying degrees of reduction in neutralization against a range of key SARS-CoV-2 variants, including variant Alpha, Beta, Gamma, Iota, and Delta. Our work show diminished neutralization potency against multiple variants in vaccine-elicited sera, which indicates the potential need for additional boost vaccinations.
【초록키워드】 SARS-CoV-2, Vaccine, coronavirus, immunogenicity, clinical trial, antibody, neutralization, variant, Delta, severe acute respiratory syndrome Coronavirus, variants, SARS-CoV-2 vaccine, vaccine dose, global pandemic, Cohort, Host immune response, SARS-CoV-2 variants, immune responses, sera, Gamma, Alpha, Beta, Neutralizing, respiratory, boost, inactivated, BBIBP-CorV, Vaccinations, Iota, Serious Adverse Events, Serious Adverse Event, acute respiratory syndrome, acute respiratory syndrome coronavirus, acute respiratory syndrome coronavirus 2, recipients, neutralization potency, Registered, host immune responses, term, recipient, indicate, reduction in, 【제목키워드】 SARS-CoV-2 variant, Delta, sera,