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标题:维持性血液透析的终末期肾病患者接种 COVID-19 疫苗的免疫原性:混合接种策略的疗效。

Immunogenicity of COVID-19 Vaccination in Patients With End-Stage Renal Disease Undergoing Maintenance Hemodialysis: The Efficacy of a Mix-and-Match Strategy.

机构信息

Department of Internal Medicine, Hanyang University College of Medicine, Seoul, Korea.

Division of Nephrology, Department of Internal Medicine, Hanyang University Seoul Hospital, Seoul, Korea.

出版信息

J Korean Med Sci. 2022 Jun 13;37(23):e180. doi: 10.3346/jkms.2022.37.e180.

Abstract

BACKGROUND

The objective of this study was to evaluate the immunogenicity of coronavirus disease 2019 (COVID-19) vaccination in patients with end-stage renal disease (ESRD) on hemodialysis.

METHODS

ESRD patients at the hemodialysis center of a tertiary-care university-affiliated hospital and healthy employees at the clinical laboratory center were prospectively recruited between March and June 2021. For severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) antibody analysis, blood samples were collected serially on days 0, 14, 28, and 56 after the first vaccine dose, and on days 7 and 50 after the second dose. Antibodies against the SARS-CoV-2 spike protein were quantified, and SARS-CoV-2 neutralizing antibodies were measured in the serum and plasma.

RESULTS

Thirty-one ESRD patients and 55 healthy employees were regularly monitored. Twenty-five (80.6%) ESRD patients on hemodialysis received a mix-and-match strategy with ChAdOx1-BNT162b2 (AZ-Pf group) and six (19.4%) received two doses of ChAdOx1 (AZ-AZ group). ESRD patients on hemodialysis showed lower binding antibody titers and neutralizing antibody activities compared to healthy participants following the first vaccination with ChAdOx1. After the second dose, AZ-Pf group had higher immunogenicity than healthy people on days 7 and 50. The binding antibody titer and neutralizing antibody activities on days 7 and 50 were significantly higher in the AZ-Pf group than in the AZ-AZ group.

CONCLUSION

ESRD patients on hemodialysis receiving the mix-and-match strategy (ChAdOx1-BNT162b2) have COVID-19 vaccine immunogenicity comparable to healthy individuals receiving two doses of ChAdOx1.

TRIAL REGISTRATION

ClinicalTrials.gov Identifier: NCT04871945.

摘要

背景

本研究旨在评估血液透析终末期肾病(ESRD)患者接种 2019 年冠状病毒病(COVID-19)疫苗的免疫原性。

方法

2021 年 3 月至 6 月,前瞻性招募了三级医院血液透析中心的 ESRD 患者和临床实验室中心的健康员工。为了进行严重急性呼吸综合征冠状病毒 2(SARS-CoV-2)抗体分析,在第 1 剂疫苗后第 0、14、28 和 56 天以及第 2 剂疫苗后第 7 和 50 天采集血样。定量检测血清和血浆中针对 SARS-CoV-2 刺突蛋白的抗体,并测量 SARS-CoV-2 中和抗体。

结果

31 名 ESRD 患者和 55 名健康员工接受了定期监测。25 名(80.6%)接受混合接种 ChAdOx1-BNT162b2(AZ-Pf 组)和 6 名(19.4%)接受两剂 ChAdOx1(AZ-AZ 组)的血液透析 ESRD 患者。与健康参与者相比,接受 ChAdOx1 首次接种后,血液透析的 ESRD 患者的结合抗体滴度和中和抗体活性较低。第二次接种后,AZ-Pf 组在第 7 天和第 50 天的免疫原性高于健康人群。与 AZ-AZ 组相比,AZ-Pf 组在第 7 天和第 50 天的结合抗体滴度和中和抗体活性均显著更高。

结论

接受混合接种策略(ChAdOx1-BNT162b2)的血液透析 ESRD 患者的 COVID-19 疫苗免疫原性可与接受两剂 ChAdOx1 的健康个体相媲美。

试验注册

ClinicalTrials.gov 标识符:NCT04871945。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e889/9194491/e0c54902ad4f/jkms-37-e180-g001.jpg

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