Yi Xuan, Wang Yuhao, Li Quanrun, Li Xiaoyi, Zhang Panli, Fu Xin, Gu Shuqin, Zhang Daqian, Liu Xiaoyi, Lou Haonan, Wu Yuemei, Tang Libo, Hou Jinlin, Li Yongyin
State Key Laboratory of Organ Failure Research, Guangdong Provincial Key Laboratory of Viral Hepatitis Research, Department of Infectious Diseases, Nanfang Hospital, Southern Medical University, Guangzhou, China.
Department of Infectious Diseases, The First Affiliated Hospital of Dali University, School of Clinical Medicine, Dali University, Dali, China.
J Med Virol. 2023 Mar;95(3):e28642. doi: 10.1002/jmv.28642.
Individuals with a recent common cold coronavirus infection, which leads to pre-existing immunity against SARS-CoV-2, displayed a less severe course of COVID-19. However, the relationship between pre-existing immunity against SARS-CoV-2 and the inactivated-vaccine-induced immune response is still unknown. Here, 31 healthcare workers who received standard two doses of inactivated COVID-19 vaccines (Weeks 0 and 4, respectively) were enrolled, vaccine-induced neutralization and T cell responses were detected, and the correlation between the pre-existing SARS-CoV-2-specific immunity was analyzed. We found the SARS-CoV-2-specific antibodies, pseudovirus neutralization test (pVNT) titers, and spike-specific interferon gamma (IFN-γ) production in CD4 and CD8 T cells were significantly elevated after two doses of inactivated vaccines. Interestingly, the pVNT titers after the second dose of vaccination displayed no significant correlation with the pre-existing SARS-CoV-2-specific antibodies or B cells, nor the pre-existing spike-specific CD4 T cells. Notably, the spike-specific T cell response after the second dose of vaccination was positively correlated with the pre-existing receptor binding domain (RBD)-specific B cells and CD4 T cells, which were documented by the frequencies of RBD-binding B cells, the breadth of RBD-specific B cell epitopes, and the frequency of IFN-γ-expressing RBD-specific CD4 T cells. Overall, the inactivated-vaccine-induced T cell responses, not the inactivated-vaccine-induced neutralization, closely correlated with pre-existing immunity to SARS-CoV-2. Our results provide a better understanding of inactivated-vaccine-induced immunity and help predict the immunogenicity induced by inactivated vaccines in individuals.
近期感染普通感冒冠状病毒从而对严重急性呼吸综合征冠状病毒2(SARS-CoV-2)产生预先存在免疫力的个体,其新冠病毒疾病(COVID-19)病程较轻。然而,针对SARS-CoV-2的预先存在免疫力与灭活疫苗诱导的免疫反应之间的关系仍不清楚。在此,招募了31名接受标准两剂次新型冠状病毒灭活疫苗(分别在第0周和第4周接种)的医护人员,检测疫苗诱导的中和反应和T细胞反应,并分析预先存在的SARS-CoV-2特异性免疫之间的相关性。我们发现,两剂次灭活疫苗接种后,SARS-CoV-2特异性抗体、假病毒中和试验(pVNT)滴度以及CD4和CD8 T细胞中刺突蛋白特异性干扰素γ(IFN-γ)的产生均显著升高。有趣的是,第二剂疫苗接种后的pVNT滴度与预先存在的SARS-CoV-2特异性抗体或B细胞,以及预先存在的刺突蛋白特异性CD4 T细胞均无显著相关性。值得注意的是,第二剂疫苗接种后的刺突蛋白特异性T细胞反应与预先存在的受体结合域(RBD)特异性B细胞和CD4 T细胞呈正相关,这通过RBD结合B细胞的频率、RBD特异性B细胞表位的广度以及表达IFN-γ的RBD特异性CD4 T细胞的频率得以证明。总体而言,灭活疫苗诱导的T细胞反应而非灭活疫苗诱导的中和反应与预先存在的SARS-CoV-2免疫力密切相关。我们的结果有助于更好地理解灭活疫苗诱导的免疫,并有助于预测灭活疫苗在个体中诱导的免疫原性。