医学
2019年冠状病毒病(COVID-19)
抗体
严重急性呼吸综合征冠状病毒2型(SARS-CoV-2)
信使核糖核酸
2019-20冠状病毒爆发
抗体反应
接种疫苗
免疫学
免疫系统
病毒学
内科学
基因
生物
爆发
传染病(医学专业)
疾病
生物化学
作者
Duaa W. Al‐Sadeq,Farah M. Shurrab,Ahmed Ismail,Fathima Humaira Amanullah,Swapna Thomas,Nader Al‐Dewik,Hadi M. Yassine,Hanan F. Abdul Rahim,Laith J. Abu‐Raddad,Gheyath K. Nasrallah
摘要
Abstract Background Two mRNA vaccines, Pfizer-BNT162b2 and Moderna-mRNA-1273, obtained the Emergency Use Listing by WHO for preventing COVID-19. However, little is known about the difference in antibody responses induced by these two mRNA vaccines in naïve and previously infected (PI) individuals. Method We investigated the levels of anti-S-RBD (total, IgG and IgA) levels in naïve and PI individuals, 1–13 (median = 6) weeks following the second dose of either vaccine. Results in the naïve-vaccinated group, the mRNA-1273 vaccine induced significantly higher levels of anti-S-RBD total antibodies (3.5-fold; P < 0.001), IgG (2-fold, P < 0.01) and IgA (2.1-fold, P < 0.001) as compared with the BNT162b2 vaccine. In addition, both vaccines produced significantly higher anti-S-RBD total antibody levels in the PI-group compared with naïve-vaccinated group. The PI group elicited a higher level of anti-S-RBD IgG than the naïve-BNT162b2 (P = 0.05), but not more than the naïve-mRNA-1273 (P = 0.9) group. Interestingly, the PI vaccinated group elicited a comparable level of IgA ratio to the naïve-mRNA-1273 group but significantly higher than the naïve-BNT162b2 group (1.6-fold, P < 0.001). Conclusion Our results showed that the PI-vaccinated group produces a higher level of antibodies than the naïve vaccinated group, particularly for those vaccinated with BNT162b2.
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