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BNT162b2 mRNA COVID-19 疫苗在成年自身免疫性炎症性风湿病患者和普通人群中的免疫原性和安全性:一项多中心研究。

Immunogenicity and safety of the BNT162b2 mRNA COVID-19 vaccine in adult patients with autoimmune inflammatory rheumatic diseases and in the general population: a multicentre study.

机构信息

Rheumatology Department, Tel Aviv Sourasky Medical Center, Tel Aviv, Israel

Tel Aviv University Sackler Faculty of Medicine, Tel Aviv, Israel.

出版信息

Ann Rheum Dis. 2021 Oct;80(10):1330-1338. doi: 10.1136/annrheumdis-2021-220647. Epub 2021 Jun 14.

Abstract

INTRODUCTION

Vaccination represents a cornerstone in mastering the COVID-19 pandemic. Data on immunogenicity and safety of messenger RNA (mRNA) vaccines in patients with autoimmune inflammatory rheumatic diseases (AIIRD) are limited.

METHODS

A multicentre observational study evaluated the immunogenicity and safety of the two-dose regimen BNT162b2 mRNA vaccine in adult patients with AIIRD (n=686) compared with the general population (n=121). Serum IgG antibody levels against SARS-CoV-2 spike S1/S2 proteins were measured 2-6 weeks after the second vaccine dose. Seropositivity was defined as IgG ≥15 binding antibody units (BAU)/mL. Vaccination efficacy, safety, and disease activity were assessed within 6 weeks after the second vaccine dose.

RESULTS

Following vaccination, the seropositivity rate and S1/S2 IgG levels were significantly lower among patients with AIIRD versus controls (86% (n=590) vs 100%, p<0.0001 and 132.9±91.7 vs 218.6±82.06 BAU/mL, p<0.0001, respectively). Risk factors for reduced immunogenicity included older age and treatment with glucocorticoids, rituximab, mycophenolate mofetil (MMF), and abatacept. Rituximab was the main cause of a seronegative response (39% seropositivity). There were no postvaccination symptomatic cases of COVID-19 among patients with AIIRD and one mild case in the control group. Major adverse events in patients with AIIRD included death (n=2) several weeks after the second vaccine dose, non-disseminated herpes zoster (n=6), uveitis (n=2), and pericarditis (n=1). Postvaccination disease activity remained stable in the majority of patients.

CONCLUSION

mRNA BNTb262 vaccine was immunogenic in the majority of patients with AIIRD, with an acceptable safety profile. Treatment with glucocorticoids, rituximab, MMF, and abatacept was associated with a significantly reduced BNT162b2-induced immunogenicity.

摘要

简介

疫苗接种是控制 COVID-19 大流行的基石。信使 RNA(mRNA)疫苗在自身免疫性炎症性风湿病(AIIRD)患者中的免疫原性和安全性数据有限。

方法

一项多中心观察性研究评估了两剂 BNT162b2 mRNA 疫苗在 AIIRD 成年患者(n=686)中的免疫原性和安全性,并与普通人群(n=121)进行了比较。在第二剂疫苗接种后 2-6 周测量针对 SARS-CoV-2 刺突 S1/S2 蛋白的血清 IgG 抗体水平。定义血清 IgG 抗体阳性为 IgG≥15 结合抗体单位(BAU)/mL。在第二剂疫苗接种后 6 周内评估疫苗接种疗效、安全性和疾病活动度。

结果

接种疫苗后,与对照组相比,AIIRD 患者的血清 IgG 抗体阳性率和 S1/S2 IgG 水平显著降低(86%(n=590)vs 100%,p<0.0001 和 132.9±91.7 vs 218.6±82.06 BAU/mL,p<0.0001)。免疫原性降低的危险因素包括年龄较大和使用糖皮质激素、利妥昔单抗、霉酚酸酯(MMF)和阿巴西普。利妥昔单抗是血清阴性反应的主要原因(39%的 IgG 抗体阳性率)。AIIRD 患者中无接种后症状性 COVID-19 病例,对照组有 1 例轻症病例。AIIRD 患者的主要不良事件包括 2 例死亡(在第二剂疫苗接种后数周)、6 例非播散性带状疱疹、2 例葡萄膜炎和 1 例心包炎。大多数患者的接种后疾病活动度保持稳定。

结论

mRNA BNTb262 疫苗在大多数 AIIRD 患者中具有免疫原性,且安全性良好。糖皮质激素、利妥昔单抗、MMF 和阿巴西普的治疗与 BNT162b2 诱导的免疫原性显著降低相关。

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