Antibody and transcription landscape in peripheral blood mononuclear cells of elderly adults over 70 years of age with third dose of COVID-19 BBIBP-CorV and ZF2001 booster vaccine

外周血单个核细胞 医学 2019年冠状病毒病(COVID-19) 抗体 助推器(火箭) 免疫学 病毒学 严重急性呼吸综合征冠状病毒2型(SARS-CoV-2) 增强剂量 2019-20冠状病毒爆发 外周血 抗体反应 传染病(医学专业) 内科学 疾病 生物 免疫 爆发 体外 物理 生物化学 天文
作者
Yuwei Zhang,Lianxiang Zhao,Jinzhong Zhang,Xiaomei Zhang,Shanshan Han,Qingshuai Sun,Mingxiao Yao,Bo Pang,Qing Duan,Xiaolin Jiang
标识
DOI:10.1186/s12979-023-00408-x
摘要

In the context of the COVID-19 pandemic and extensive vaccination, it is important to explore the immune response of elderly adults to homologous and heterologous booster vaccines of COVID-19. At this point, we detected serum IgG antibodies and PBMC sample transcriptome profiles in 46 participants under 70 years old and 25 participants over 70 years old who received the third dose of the BBIBP-CorV and ZF2001 vaccines.On day 7, the antibody levels of people over 70 years old after the third dose of booster vaccine were lower than those of young people, and the transcriptional responses of innate and adaptive immunity were also weak. The age of the participants showed a significant negative correlation with functions related to T-cell differentiation and costimulation. Nevertheless, 28 days after the third dose, the IgG antibodies of elderly adults reached equivalence to those of younger adults, and immune-related transcriptional regulation was significantly improved. The age showed a significant positive correlation with functions related to "chemokine receptor binding", "chemokine activity", and "chemokine-mediated signaling pathway".Our results document that the response of elderly adults to the third dose of the vaccine was delayed, but still able to achieve comparable immune effects compared to younger adults, in regard to antibody responses as well as at the transcript level.

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