Department of Rheumatology, Shenzhen Futian Hospital for Rheumatic Diseases, Shenzhen, Guangdong, China.
Guangzhou Yusu Biomedical Technology Co., Haizhu District, Guangzhou, China.
Hum Vaccin Immunother. 2022 Nov 30;18(5):2090176. doi: 10.1080/21645515.2022.2090176. Epub 2022 Jul 25.
Patients with rheumatic diseases (RD) are considered to be a high-risk population for infection with the severe acute respiratory syndrome coronavirus-2 (SARS-CoV-2). The effectiveness of inactivated COVID-19 vaccinations (ICVs) was described as more effective than 95%. Despite this, no data on the immunogenicity and safety of the ICV in Han race stable RD patients in China. In this study, we sought to assess the safety and immunogenicity of the ICVs in RD patients in South China. A total of 80 adult stable RD patients were recruited. Following 14-35 days of immunization, cheiluminescence immunoassays (CLIA) were utilized to detect antibodies titers. An investigation into the relative parameters on the immunogenicity response to vaccination was carried out using logistic regression analysis. Compared to the HC group, the positive response of IgG and Nab in RD patients were lower than those in healthy control (HC) ( = .040 and < .0001, respectively) after two doses of ICV were inoculated. The use of methotrexate ( = .016) and prednisolone ( = .018), and the level of red blood cell distribution width-C (RDW-C) ( = .035) and C-reactive protein ( = .015) were independently associated with lower rises in the magnitude of COVID-19 vaccine antibodies. No vaccine-related serious adverse reactions were observed in either group. After receiving two doses of ICVs, the production of protective antibodies in stable RD patients treated with immunosuppressive agents may decrease. It was discovered that ICVs were safe and well tolerated by RD patients.
患有风湿性疾病(RD)的患者被认为是感染严重急性呼吸综合征冠状病毒 2(SARS-CoV-2)的高危人群。已描述灭活 COVID-19 疫苗(ICV)的有效性超过 95%。尽管如此,在中国汉族稳定 RD 患者中,尚未有关于 ICV 的免疫原性和安全性的数据。在这项研究中,我们旨在评估 ICV 在华南 RD 患者中的安全性和免疫原性。共招募了 80 名成年稳定 RD 患者。免疫接种后 14-35 天,使用化学发光免疫分析(CLIA)检测抗体滴度。使用逻辑回归分析对疫苗接种免疫应答的相对参数进行了调查。与 HC 组相比,接种两剂 ICV 后,RD 患者 IgG 和 Nab 的阳性反应均低于健康对照组(HC)(=0.040 和 <0.0001)。使用甲氨蝶呤(=0.016)和泼尼松龙(=0.018),以及红细胞分布宽度-C(RDW-C)(=0.035)和 C 反应蛋白(=0.015)水平与 COVID-19 疫苗抗体幅度的降低呈独立相关。两组均未观察到与疫苗相关的严重不良反应。接受两剂 ICV 后,接受免疫抑制剂治疗的稳定 RD 患者产生保护性抗体的能力可能会降低。研究发现,ICV 对 RD 患者是安全且耐受良好的。