COVID-19 vaccination of patients with chronic immune-mediated inflammatory disease.

IF 4.6 Q2 MATERIALS SCIENCE, BIOMATERIALS
Wen Yanfang, Chen Jianfeng, Liu Changlian, Wang Yan
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引用次数: 1

Abstract

Objective: This study aimed to analyze the safety and efficacy of COVID-19 vaccines among patients with chronic immune-mediated inflammatory disease (IMID) in China.

Methods: Participants who were diagnosed with a chronic IMID were eligible for inclusion in this study. Age- and sex-matched healthy vaccinated individuals were set as the control group. All participants received two doses of the inactivated CoronaVac vaccine or three doses of the recombinant protein subunit vaccine ZF2001. Adverse events, IMID activity after vaccination, and the rate of COVID-19 in the two groups were compared.

Results: There were 158 patients in the IMID group, with an average age of 40 ± 14 years old, and 98 female subjects. In the IMID group, 123 patients received the inactivated CoronaVac vaccine, and 35 patients received the recombinant protein subunit vaccine ZF2001. There were 153 individuals in the control group, including 122 who received the CoronaVac vaccine and 31 who received the recombinant protein subunit vaccine ZF2001. The frequency of vaccine-related adverse events in the IMID group was less than that in the control group, all of which were mild local effects, and no serious events occurred. Of note, no disease flares occurred in the IMID group. No participants in either group subsequently got COVID-19, so the incidence rate was 0% in both groups.

Conclusion: COVID-19 vaccination was found to be safe for IMID subjects, any adverse events were mild, and vaccination did not increase the risk of disease activity. Meanwhile, vaccination could effectively reduce the incidence of COVID-19 in IMID patients. In the future, studies with a larger sample size and a longer duration are needed.

慢性免疫介导炎症性疾病患者的新冠肺炎疫苗接种。
目的:本研究旨在分析新冠肺炎疫苗在中国慢性免疫介导炎症性疾病(IMID)患者中的安全性和有效性。年龄和性别匹配的健康接种者被设定为对照组。所有参与者都接种了两剂灭活的CoronaVac疫苗或三剂重组蛋白亚单位疫苗ZF2001。比较两组的不良事件、接种后IMID活性和新冠肺炎发病率。结果:IMID组共有158名患者,平均年龄为40岁 ± 14岁和98名女性受试者。在IMID组中,123名患者接受了灭活的CoronaVac疫苗,35名患者接受重组蛋白亚单位疫苗ZF2001。对照组共有153人,其中122人接种了CoronaVac疫苗,31人接种了重组蛋白亚单位疫苗ZF2001。IMID组的疫苗相关不良事件发生频率低于对照组,均为轻度局部反应,未发生严重事件。值得注意的是,IMID组未出现疾病发作。两组中没有任何参与者随后感染新冠肺炎,因此两组的发病率均为0%。结论:新冠肺炎疫苗接种对IMID受试者是安全的,任何不良事件都是轻微的,疫苗接种不会增加疾病活动的风险。同时,接种疫苗可以有效降低IMID患者的新冠肺炎发病率。未来需要更大样本量和更长持续时间的研究。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
ACS Applied Bio Materials
ACS Applied Bio Materials Chemistry-Chemistry (all)
CiteScore
9.40
自引率
2.10%
发文量
464
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