Li Jiazhi, Cao Peihua, Chen Zhenhu, Deng Ruihua, Nie Yu, Pang Feixiong, Liu Xiaomian, Huang Haijia, Yang Jianrong, Zhong Kebo, Lai Yanhua
Department of Transplantation, The People's Hospital of Guangxi Zhuang Autonomous Region, Nanning 530021, Guangxi, China.
Clinical Research Center, Zhujiang Hospital, Southern Medical University, Guangzhou 510280, Guangdong, China.
Open Med (Wars). 2024 Jun 18;19(1):20240980. doi: 10.1515/med-2024-0980. eCollection 2024.
This study aimed to evaluate the efficacy and safety of solid organ transplantation recipients inoculated with an inactivated COVID-19 vaccine.
We retrospectively analyzed the antibody levels and related adverse events of non-transplantation subjects and solid organ transplant recipients, both pre-transplantation (individuals awaiting organ transplantation) and post-transplantation (individuals who have undergone organ transplantation), who received inactivated COVID-19 vaccines from February 2021 to July 2022.
The study included 38 pre-transplantation vaccination group, 129 post-transplantation vaccination group, and 246 non-transplantation group. The antibody titer was assessed monthly within the period of 1-12 months after the last injection. The antibody-positive rate among the three groups were 36.84, 20.30, 61.17% ( < 0.05). The antibody-positive rates among three groups with one, two doses vaccine were not significantly different ( > 0.05), but were significantly different after three doses ( < 0.05). The antibody titers among three groups were significantly different after two doses ( < 0.05). Adverse reactions occurred in six transplant recipients, which were relieved after treatment, and not in the non-transplantation subjects.
Inactivated COVID-19 vaccine is safe and effective for solid organ transplantation recipients, at least two doses of which should be completed before organ transplant surgery.
本研究旨在评估实体器官移植受者接种新型冠状病毒灭活疫苗(COVID-19疫苗)的有效性和安全性。
我们回顾性分析了2021年2月至2022年7月期间接受新型冠状病毒灭活疫苗接种的非移植受者、移植前(等待器官移植者)和移植后(已接受器官移植者)实体器官移植受者的抗体水平及相关不良事件。
本研究纳入移植前接种疫苗组38例、移植后接种疫苗组129例和非移植组246例。在最后一剂接种后的1至12个月内每月评估抗体滴度。三组的抗体阳性率分别为36.84%、20.30%、61.17%(P<0.05)。接种一剂、两剂疫苗的三组间抗体阳性率差异无统计学意义(P>0.05),但接种三剂后差异有统计学意义(P<0.05)。接种两剂后三组间抗体滴度差异有统计学意义(P<0.05)。6例移植受者出现不良反应,经治疗后缓解,非移植受者未出现不良反应。
新型冠状病毒灭活疫苗对实体器官移植受者安全有效,在器官移植手术前至少应完成两剂接种。