Antibody response to COVID-19 vaccination in patients on chronic hemodialysis.

IF 2.1 Q4 IMMUNOLOGY
Heejung Choi, Sungdam Han, Ji Su Kim, Bumhee Park, Min-Jeong Lee, Gyu-Tae Shin, Heungsoo Kim, Kyongmin Kim, A-Young Park, Ho-Joon Shin, Inwhee Park
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引用次数: 1

Abstract

Purpose: Since patients on hemodialysis (HD) are known to be vulnerable to coronavirus disease 2019 (COVID-19), many studies were conducted regarding the effectiveness of the COVID-19 vaccine in HD patients in Western countries. Here, we assessed antibody response of HD patients for 6 months post-vaccination to identify the duration and effectiveness of the COVID-19 vaccine in the Asian population.

Materials and methods: We compared antibody response of the COVID-19 vaccine in HD patients with healthy volunteers. Patient and control groups had two doses of ChAdOx1 nCoV-19 and mRNA-1273, respectively. Immunoglobulin G (IgG) was measured before vaccination, 2 weeks after the first dose, 2 and 4 weeks, 3 and 6 months after the second dose. Neutralizing antibody was measured before vaccination and at 2 weeks, 3 and 6 months after second dose. Since the third dose was started in the middle of the study, we analyzed the effect of the third dose as well.

Results: Although antibody production was weaker than the control group (n=22), the patient group (n=39) showed an increase in IgG and neutralizing antibody after two doses. And, 21/39 patients and 14/22 participants had a third dose (BNT162b2 or mRNA-1273 in the patient group, mRNA-1273 in the control group), and it did not affect antibody response in both group. Trend analysis showed IgG and neutralizing antibody did not decrease over time. Age, sex, and HD vintage did not affect antibody production in HD patients. Patients with higher body mass index displayed better seroresponse, while those on immunosuppressants showed poor seroresponse.

Conclusion: Two doses of vaccination led to significant antibody response in HD patients, and the antibody did not wane until 6 months.

Abstract Image

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慢性血液透析患者对COVID-19疫苗接种的抗体反应
目的:由于血液透析(HD)患者易感染2019冠状病毒病(COVID-19),西方国家开展了许多关于COVID-19疫苗在HD患者中的有效性的研究。在这里,我们评估了HD患者在接种疫苗后6个月的抗体反应,以确定COVID-19疫苗在亚洲人群中的持续时间和有效性。材料与方法:比较HD患者与健康志愿者COVID-19疫苗的抗体反应。患者组和对照组分别使用两剂ChAdOx1 nCoV-19和mRNA-1273。免疫球蛋白G (IgG)分别于接种前、第一次接种后2周、第二次接种后2、4周、3、6个月测定。在接种前和第二次接种后2周、3和6个月测定中和抗体。由于第三次剂量是在研究中期开始的,我们也分析了第三次剂量的效果。结果:虽然抗体产生较对照组(n=22)弱,但患者组(n=39)在两次给药后IgG和中和抗体均增加。并且,21/39名患者和14/22名参与者接受了第三次剂量(患者组为BNT162b2或mRNA-1273,对照组为mRNA-1273),它不影响两组的抗体反应。趋势分析显示IgG和中和抗体不随时间降低。年龄、性别和HD年份对HD患者的抗体产生没有影响。体质指数较高的患者血清反应较好,而免疫抑制剂组血清反应较差。结论:两剂疫苗接种可使HD患者产生明显的抗体应答,且抗体在6个月后才减弱。
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来源期刊
CiteScore
3.70
自引率
3.70%
发文量
29
审稿时长
8 weeks
期刊介绍: Clin Exp Vaccine Res, the official English journal of the Korean Vaccine Society, is an international, peer reviewed, and open-access journal. It covers all areas related to vaccines and vaccination. Clin Exp Vaccine Res publishes editorials, review articles, special articles, original articles, case reports, brief communications, and correspondences covering a wide range of clinical and experimental subjects including vaccines and vaccination for human and animals against infectious diseases caused by viruses, bacteria, parasites and tumor. The scope of the journal is to disseminate information that may contribute to elaborate vaccine development and vaccination strategies targeting infectious diseases and tumors in human and animals. Relevant topics range from experimental approaches to (pre)clinical trials for the vaccine research based on, but not limited to, basic laboratory, translational, and (pre)clinical investigations, epidemiology of infectious diseases and progression of all aspects in the health related issues. It is published printed and open accessed online issues (https://ecevr.org) two times per year in 31 January and 31 July. Clin Exp Vaccine Res is linked to many international databases and is made freely available to institutions and individuals worldwide
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