Longitudinal assessment of immunogenicity of inactivated COVID-19 booster immunization and breakthrough infection in blood donors: A multicenter study from 2021 to 2023
Assessing immune responses across diverse populations is essential for refining public health strategies. Blood donors offer valuable insights into community-level immunity. This study aims to investigate immune responses associated with inactivated COVID-19 booster immunization and breakthrough infections in blood donors. This study was conducted in a cohort of blood donors from six centers across five of China's seven major geographical regions, spanning from December 2021 to February 2023. Blood samples were collected before booster vaccination, at 1, 3, and 6 months post-vaccination, as well as 1 month post-infection. SARS-CoV-2-specific antibodies, T cell specific IFNγ levels, and neutralizing antibodies against wild-type and Omicron strains were measured. Platelet count, anti-PF4 antibody, and D-dimer levels were assessed. Demographic characteristics were analyzed to determine their impact on immunogenicity. SARS-CoV-2-specific antibodies and IFNγ levels significantly increased post-booster, peaking one month after immunization. Antibodies continued to decrease at six months, while IFNγ levels remained stable at this point. Pseudovirus neutralization assays revealed elevated neutralizing antibodies following the booster dose, with minimal response to the XBB.1.5 variant. Following Omicron infection, antibody and IFNγ levels surpassed that observed post-booster. Participants aged 36-49 and those over 50 exhibited weaker immune responses post-booster than those ages 18-35, while those with BMI above 28 showed lower IFNγ levels. This study demonstrates the utility of blood donor samples for tracking immunization effectiveness against emerging pathogens, and highlights enhanced immune responses after booster immunization and breakthrough infections, underscoring the need for tailored vaccination strategies for different groups.
Authors
- Baifeng Shan
- Xuelian Deng
- Ying Yan (ORCID: https://orcid.org/0000-0001-8556-7417)
- Lunan Wang (ORCID: https://orcid.org/0000-0003-3163-7891)
- Lei Zhao (ORCID: https://orcid.org/0000-0002-9878-4530)
- Chuanbao Li (ORCID: https://orcid.org/0000-0002-1224-0509)
- Huimin Ji (ORCID: https://orcid.org/0000-0001-7790-1550)
- Yinkai Duan (ORCID: https://orcid.org/0000-0002-0544-7413)
- Xianzhang Bu
- Le Chang (ORCID: https://orcid.org/0000-0002-6154-7304)
- Shana Halemubieke
- Libo Zhang (ORCID: https://orcid.org/0000-0002-2972-5174)
- Lin Wang (ORCID: https://orcid.org/0000-0001-5716-6587)
- Ying Liu (ORCID: https://orcid.org/0000-0002-6540-0473)
- Peng Sun (ORCID: https://orcid.org/0000-0002-0095-4782)
- Yifang Wang (ORCID: https://orcid.org/0000-0002-4788-5999)
- Qiang Wang (ORCID: https://orcid.org/0000-0001-9409-0251)
- Huizhen Sun (ORCID: https://orcid.org/0000-0001-8533-4349)
- Yang Liu (ORCID: https://orcid.org/0000-0003-4350-8448)
- Ming‐Jie Wu
Institutions
- Academy of Medical Sciences (GB)
- Chinese Academy of Medical Sciences & Peking Union Medical College (CN)
- Beijing Hospital (CN)
- Beijing Red Cross Blood Center (CN)
Publication Details
- Journal
- Human Vaccines & Immunotherapeutics
- Published
- 2025-05-05
- DOI
- https://doi.org/10.1080/21645515.2025.2498828
- Primary Topic
- SARS-CoV-2 and COVID-19 Research
- Type
- article
- Field-Weighted Citation Impact
- 0.00
Funders
- Natural Science Foundation of Beijing Municipality