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免疫抑制治疗患者中疫苗和混合免疫后 COVID-19 的发生率和结局:前瞻性队列研究中识别免疫后抗 RBD 抗体的保护性水平。

Incidence and outcome of COVID-19 following vaccine and hybrid immunity in patients on immunosuppressive therapy: identification of protective post-immunisation anti-RBD antibody levels in a prospective cohort study.

机构信息

Center for treatment of Rheumatic and Musculoskeletal Diseases (REMEDY), Diakonhjemmet Hospital, Oslo, Norway

Institute of Clinical Medicine, Faculty of Medicine, University of Oslo, Oslo, Norway.

出版信息

RMD Open. 2024 Apr 9;10(2):e003545. doi: 10.1136/rmdopen-2023-003545.

Abstract

OBJECTIVES

To assess incidence, severity and predictors of COVID-19, including protective post-vaccination levels of antibodies to the receptor-binding domain of SARS-CoV-2 spike protein (anti-RBD), informing further vaccine strategies for patients with immune-mediated inflammatory diseases (IMIDs) on immunosuppressive medication.

METHODS

IMIDs on immunosuppressives and healthy controls (HC) receiving SARS-CoV-2 vaccines were included in this prospective observational study. COVID-19 and outcome were registered and anti-RBD antibodies measured 2-5 weeks post-immunisation.

RESULTS

Between 15 February 2021 and 15 February 2023, 1729 IMIDs and 350 HC provided blood samples and self-reported COVID-19. The incidence of COVID-19 was 66% in patients and 67% in HC, with re-infection occurring in 12% of patients. Severe COVID-19 was recorded in 22 (2%) patients and no HC. No COVID-19-related deaths occurred. Vaccine-induced immunity gave higher risk of COVID-19 (HR 5.89 (95% CI 4.45 to 7.80)) than hybrid immunity. Post-immunisation anti-RBD levels <6000 binding antibody units/mL were associated with an increased risk of COVID-19 following three (HR 1.37 (95% CI 1.08 to 1.74)) and four doses (HR 1.28 (95% CI 1.02 to 1.62)), and of COVID-19 re-infection (HR 4.47 (95% CI 1.87 to 10.67)).

CONCLUSION

Vaccinated patients with IMID have a low risk of severe COVID-19. Hybrid immunity lowers the risk of infection. High post-immunisation anti-RBD levels protect against COVID-19. These results suggest that knowledge on COVID-19 history, and assessment of antibody levels post-immunisation can help individualise vaccination programme series in high-risk individuals.

TRIAL REGISTRATION NUMBER

NCT04798625.

摘要

目的

评估 COVID-19 的发病率、严重程度和预测因素,包括针对 SARS-CoV-2 刺突蛋白受体结合域的抗体(抗-RBD)的保护性接种后水平,为接受免疫抑制药物治疗的免疫介导的炎症性疾病(IMID)患者提供进一步的疫苗接种策略。

方法

本前瞻性观察性研究纳入了正在接受免疫抑制剂治疗的 IMID 患者和接受 SARS-CoV-2 疫苗的健康对照(HC)。登记 COVID-19 及结局,并在接种后 2-5 周测量抗-RBD 抗体。

结果

2021 年 2 月 15 日至 2023 年 2 月 15 日,共纳入 1729 名 IMID 患者和 350 名 HC,提供血样并报告 COVID-19 情况。患者的 COVID-19 发病率为 66%,HC 为 67%,患者中有 12%发生再感染。记录到 22 例(2%)患者和无 HC 发生严重 COVID-19。无 COVID-19 相关死亡。疫苗诱导的免疫使 COVID-19 的风险更高(HR 5.89(95%CI 4.45 至 7.80)),而混合免疫则较低。接种后抗-RBD 水平<6000 结合抗体单位/mL 与接种三剂(HR 1.37(95%CI 1.08 至 1.74))和四剂(HR 1.28(95%CI 1.02 至 1.62))疫苗后 COVID-19 的风险增加相关,也与 COVID-19 再感染的风险增加相关(HR 4.47(95%CI 1.87 至 10.67))。

结论

接受免疫抑制药物治疗的 IMID 患者 COVID-19 重症风险低。混合免疫降低感染风险。高接种后抗-RBD 水平可预防 COVID-19。这些结果表明,了解 COVID-19 病史,并评估接种后抗体水平,可以帮助高危人群个体化疫苗接种方案。

试验注册号

NCT04798625。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/446f/11015197/09647f2855f5/rmdopen-2023-003545f01.jpg

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