Potent Antibody Response Elicited by a Third Booster Dose of Inactivated COVID-19 Vaccine in Healthy Subjects

• Published in: Viral immunology Vol. 36; no. 9; p. 593
• Main Authors: Ji, Ruili, Zhang, Jiaqi, Liang, Dan, Quan, Hongbing, Wu, Yue, Peng, Aiping, Li, Weili, Lu, Shaofang, Zhang, Xuedong, Ke, Changwen, Wang, Dawei, Xu, Jianhua
• Format: Journal Article
• Language: English
• Published: United States 01.11.2023
• Subjects: Aged; Antibodies, Neutralizing; Antibodies, Viral; Antibody Formation; COVID-19 - prevention & control; COVID-19 Vaccines; Female; Healthy Volunteers; Humans; Immunoglobulin M; Male; Prospective Studies; SARS-CoV-2; Vaccination; booster vaccination; neutralizing antibody; SARS-CoV-2; antibody response; inactivated SARS-CoV-2 vaccine
• ISSN: 1557-8976
• DOI: 10.1089/vim.2023.0072

The severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) vaccine has been used worldwide on a large scale because of its potent ability to contain the coronavirus disease 2019 (COVID-19) pandemic, and the antibody response induced by the vaccine needs to be elucidated. Thus, we conducted a prospective trial in healthy subjects to observe the antibody response after three doses of inactivated vaccines. Our results showed that neutralizing antibody (NAb) levels were significantly higher after the booster vaccination compared to the second, a 4.9-fold increase, with the peak occurring at 28 days. The NAb level could be maintained for a longer period after the third vaccination, with higher levels still observed after 3 months. We did not observe significantly higher levels of SARS-CoV-2 spike-specific immunoglobulin G (S-IgG) and immunoglobulin M (IgM) after the third vaccination compared with the second vaccination; this was especially true for SARS-CoV-2 spike-specific immunoglobulin M (S-IgM), which was barely expressed. Notably, those who did not undergo NAb seroconversion after two doses of the vaccine produced high and long-lasting NAb after the third vaccination, confirming that they were not completely unresponsive to the vaccine. The NAb titer in younger subjects (aged 20-40 years) rose 3.4-fold compared with older subjects (aged 40-60 years) after the second vaccination, but the difference was narrowed after the third vaccination (2.8-fold increase). In addition, the levels of antibodies in older men were 3.4-fold lower than those in the older women after the third vaccination. Overall, this study elucidates the dynamic change in antibodies after three doses of vaccination, which provides a reference for the improvement of vaccination strategies.