Hsiao Shih-Hsin, Sue Yuh-Mou, Kao Chih-Chin, Chang Hui-Wen, Lin Yen-Chung, Hung Ching-Sheng, Hsieh Yi-Chen, Hong Shiao-Ya, Chung Chi-Li, Chang Jer-Hwa, Su Ying-Shih, Liu Ming-Che, Lai Kevin Shu-Leung, Chien Ko-Ling, Wang Jude Chu-Chun, Cheng Chung-Yi, Fang Te-Chao
Division of Pulmonary Medicine, Department of Internal Medicine, School of Medicine, College of Medicine, Taipei Medical University, Taipei 11031, Taiwan.
Division of Pulmonary Medicine, Department of Internal Medicine, Taipei Medical University Hospital, Taipei 11031, Taiwan.
Vaccines (Basel). 2023 Jun 27;11(7):1161. doi: 10.3390/vaccines11071161.
Hemodialysis patients are at an increased risk of SARS-CoV-2 infection and are excluded from preauthorization COVID-19 vaccine trials; therefore, their immunogenicity is uncertain.
To compare the antibody responses to homologous ChAdOx1 and mRNA-1273 SARS-CoV-2 vaccination in hemodialysis patients, 103 age- and sex-matched hemodialysis patients with two homologous prime-boost vaccinations were recruited to detect anti-receptor-binding domain (RBD) IgG levels and seroconversion rates (SCRs) 14 days after a prime dose (PD14), before and 28 days after a boost dose (pre-BD0 and BD28).
Both mRNA-1273 and ChAdOx1 vaccinations elicited immunogenicity in study subjects, and the former induced higher anti-RBD IgG levels than the latter. The SCRs of both groups increased over time and varied widely from 1.82% to 97.92%, and were significantly different at PD14 and pre-BD0 regardless of different thresholds. At BD28, the SCRs of the ChAdOx1 group and the mRNA-1273 group were comparable using a threshold ≥ 7.1 BAU/mL (93.96% vs. 97.92%) and a threshold ≥ 17 BAU/mL (92.73% vs. 97.92%), respectively, but they were significantly different using a threshold ≥ 20.2% of convalescent serum anti-RBD levels (52.73% vs. 95.83%). The seroconversion (≥20.2% of convalescent level) at BD28 was associated with mRNA-1273 vaccination after being adjusted for age, sex, body mass index, and the presence of solicited reactogenicity after a prime vaccination.
Our prospective, observational cohort indicates that a full prime-boost mRNA-1273 vaccination is likely to provide higher immune protection in hemodialysis patients compared to ChAdOx1, and this population with a prime-boost ChAdOx1 vaccination should be prioritized for a third dose.
血液透析患者感染严重急性呼吸综合征冠状病毒2(SARS-CoV-2)的风险增加,且被排除在新冠病毒疫苗预先批准试验之外;因此,其免疫原性尚不确定。
为比较血液透析患者对同源腺病毒载体疫苗ChAdOx1和信使核糖核酸疫苗mRNA-1273接种SARS-CoV-2后的抗体反应,招募了103名年龄和性别匹配的血液透析患者,进行两次同源的初免-加强接种,分别在初免剂量后14天(PD14)、加强剂量前和加强剂量后28天(预BD0和BD28)检测抗受体结合域(RBD)IgG水平和血清转化率(SCRs)。
mRNA-1273和ChAdOx1疫苗接种均在研究对象中引发了免疫原性,且前者诱导的抗RBD IgG水平高于后者。两组的血清转化率均随时间增加,范围从1.82%到97.92%广泛变化,且在PD14和预BD0时,无论采用何种阈值均有显著差异。在BD28时,ChAdOx1组和mRNA-1273组的血清转化率,在阈值≥7.1 BAU/mL时相当(93.96%对97.92%),在阈值≥17 BAU/mL时也相当(92.73%对97.92%),但在阈值≥康复期血清抗RBD水平的20.2%时存在显著差异(52.73%对95.83%)。在对年龄、性别、体重指数和初免接种后是否存在预期的反应原性进行调整后,BD28时的血清转化(≥康复期水平的20.2%)与mRNA-1273疫苗接种有关。
我们的前瞻性观察队列表明,与ChAdOx1相比,完整的初免-加强mRNA-1273疫苗接种可能为血液透析患者提供更高的免疫保护,且接受初免-加强ChAdOx1疫苗接种的这一人群应优先接种第三剂疫苗。