Balsby Daniel, Nilsson Anna Christine, Möller Sören, Lindvig Susan Olaf, Davidsen Jesper Rømhild, Abazi Rozeta, Poulsen Mikael Kjær, Holden Inge Kristine, Justesen Ulrik Stenz, Bistrup Claus, Johansen Isik Somuncu
Department of Infectious Diseases, Odense University Hospital, 5000 Odense, Denmark.
Department of Clinical Research, University of Southern Denmark, 5000 Odense, Denmark.
Vaccines (Basel). 2022 Apr 6;10(4):565. doi: 10.3390/vaccines10040565.
We studied factors related to humoral response in solid organ transplant (SOT) recipients following a three-dose regimen of an mRNA-based SARS-CoV-2 vaccine.
This was a prospective study of SOT recipients who received a third homologous dose of the BNT162b2 (Pfizer-BioNTech) vaccine. The anti-spike S1 IgG response was measured using the SARS-CoV-2 IgG II Quant assay (Abbott Laboratories) with a cut-off of 7.1 BAU/mL. Multiple logistic regression was used to determine the factors associated with humoral response.
In total, 395 SOT recipients were included. Anti-spike IgG was detected in 195/395 (49.4%) patients after the second dose and 261/335 (77.9%) patients after the third dose. The overall mean increase in antibody concentration after the third dose was 831.0 BAU/mL (95% confidence interval (CI) 687.4-974.5) and 159 (47.5%) participants had at least a 10-fold increase in antibody concentration after the third dose. The increase in antibody concentration was significantly higher among patients with detectable antibodies after the second dose than those without. Cumulative time from transplantation and liver recipients was positively associated with an antibody response, whereas older age, administration of prednisolone, and proliferation inhibitors were associated with diminished antibody response.
Although the third dose of the BNT162b2 vaccine improved humoral responses among SOT non-responders following the second dose, the overall response remained low, and 22.1% did not develop any response. Patients at risk of a diminished vaccine response require repeated booster doses and alternative treatment approaches.
我们研究了实体器官移植(SOT)受者在接种三剂基于mRNA的SARS-CoV-2疫苗后的体液免疫反应相关因素。
这是一项针对接受第三剂同源BNT162b2(辉瑞-生物科技)疫苗的SOT受者的前瞻性研究。使用SARS-CoV-2 IgG II定量检测法(雅培实验室)测量抗刺突S1 IgG反应,临界值为7.1 BAU/mL。采用多因素逻辑回归确定与体液免疫反应相关的因素。
共纳入395名SOT受者。第二剂疫苗后,195/395(49.4%)的患者检测到抗刺突IgG,第三剂疫苗后,261/335(77.9%)的患者检测到抗刺突IgG。第三剂疫苗后抗体浓度的总体平均增加为831.0 BAU/mL(95%置信区间(CI)687.4-974.5),159名(47.5%)参与者在第三剂疫苗后抗体浓度至少增加了10倍。第二剂疫苗后可检测到抗体的患者中,抗体浓度的增加显著高于未检测到抗体的患者。移植后的累积时间和肝脏受者与抗体反应呈正相关,而年龄较大、使用泼尼松龙和增殖抑制剂与抗体反应减弱相关。
尽管第三剂BNT162b2疫苗改善了第二剂疫苗后无反应的SOT受者的体液免疫反应,但总体反应仍然较低,22.1%的患者未产生任何反应。疫苗反应减弱风险较高的患者需要重复接种加强针和采用替代治疗方法。