Immunogenicity, safety and immune persistence of the sequential booster with the recombinant protein-based COVID-19 vaccine (CHO cell) in healthy people aged 18-84 years.
10.3760/cma.j.cn112150-20230423-00317
- Author:
Ding Yan YAO
1
;
Ying Ping CHEN
2
;
Fan DING
3
;
Xiao Song HU
2
;
Zhen Zhen LIANG
2
;
Bo XING
2
;
Yi Fei CAO
1
;
Tian Qi ZHANG
3
;
Xi Lu WANG
3
;
Yu Ting LIAO
4
;
Juan YANG
4
;
Hua Kun LYU
2
Author Information
1. School of Public Health, Hangzhou Normal University, Hangzhou 311121, China.
2. Department of Immunization Program, Zhejiang Provincial Center for Disease Control and Prevention, Hangzhou 310051, China.
3. Anhui Zhifei Longcom Biopharmaceutical Company, Hefei 230088, China.
4. State Key Laboratory of Molecular Vaccinology and Molecular Diagnostics/National Institute of Diagnostics and Vaccine Development in Infectious Diseases/School of Public Health, Xiamen University, Xiamen 361104, China.
- Publication Type:Journal Article
- MeSH:
Male;
Cricetinae;
Animals;
Humans;
Adult;
Middle Aged;
Female;
COVID-19 Vaccines;
Immunization, Secondary;
CHO Cells;
COVID-19/prevention & control*;
Recombinant Proteins;
Antibodies, Viral;
Antibodies, Neutralizing
- From:
Chinese Journal of Preventive Medicine
2024;58(1):25-32
- CountryChina
- Language:Chinese
-
Abstract:
Objective: To evaluate the immunogenicity, safety, and immune persistence of the sequential booster with the recombinant protein-based COVID-19 vaccine (CHO cell) in healthy people aged 18-84 years. Methods: An open-label, multi-center trial was conducted in October 2021. The eligible healthy individuals, aged 18-84 years who had completed primary immunization with the inactivated COVID-19 vaccine 3 to 9 months before, were recruited from Shangyu district of Shaoxing and Kaihua county of Quzhou, Zhejiang province. All participants were divided into three groups based on the differences in prime-boost intervals: Group A (3-4 months), Group B (5-6 months) and Group C (7-9 months), with 320 persons per group. All participants received the recombinant COVID-19 vaccine (CHO cell). Blood samples were collected before the vaccination and after receiving the booster at 14 days, 30 days, and 180 days for analysis of GMTs, antibody positivity rates, and seroconversion rates. All adverse events were collected within one month and serious adverse events were collected within six months. The incidences of adverse reactions were analyzed after the booster. Results: The age of 960 participants was (52.3±11.5) years old, and 47.4% were males (455). The GMTs of Groups B and C were 65.26 (54.51-78.12) and 60.97 (50.61-73.45) at 14 days after the booster, both higher than Group A's 44.79 (36.94-54.30) (P value<0.05). The GMTs of Groups B and C were 23.95 (20.18-28.42) and 27.98 (23.45-33.39) at 30 days after the booster, both higher than Group A's 15.71 (13.24-18.63) (P value <0.05). At 14 days after the booster, the antibody positivity rates in Groups A, B, and C were 91.69% (276/301), 94.38% (302/320), and 93.95% (295/314), respectively. The seroconversion rates in the three groups were 90.37% (272/301), 93.75% (300/320), and 93.31% (293/314), respectively. There was no significant difference among these rates in the three groups (all P values >0.05). At 30 days after the booster, antibody positivity rates in Groups A, B, and C were 79.60% (238/299), 87.74% (279/318), and 90.48% (285/315), respectively. The seroconversion rates in the three groups were 76.92% (230/299), 85.85% (273/318), and 88.25% (278/315), respectively. There was a significant difference among these rates in the three groups (all P values <0.001). During the sequential booster immunization, the incidence of adverse events in 960 participants was 15.31% (147/960), with rates of about 14.38% (46/320), 17.50% (56/320), and 14.06% (45/320) in Groups A, B, and C, respectively. The incidence of adverse reactions was 8.02% (77/960), with rates of about 7.50% (24/320), 6.88% (22/320), and 9.69% (31/320) in Groups A, B, and C, respectively. No serious adverse events related to the booster were reported. Conclusion: Healthy individuals aged 18-84 years, who had completed primary immunization with the inactivated COVID-19 vaccine 3 to 9 months before, have good immunogenicity and safety profiles following the sequential booster with the recombinant COVID-19 vaccine (CHO cell).
