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高龄、高滴度中和抗体以及使用传统改善病情抗风湿药治疗与类风湿关节炎患者在接种抗SARS-CoV-2疫苗加强针后免受突破性感染有关。

Older Age, a High Titre of Neutralising Antibodies and Therapy with Conventional DMARDs Are Associated with Protection from Breakthrough Infection in Rheumatoid Arthritis Patients after the Booster Dose of Anti-SARS-CoV-2 Vaccine.

作者信息

Picchianti-Diamanti Andrea, Navarra Assunta, Aiello Alessandra, Laganà Bruno, Cuzzi Gilda, Salmi Andrea, Vanini Valentina, Maggi Fabrizio, Meschi Silvia, Matusali Giulia, Notari Stefania, Agrati Chiara, Salemi Simonetta, Di Rosa Roberta, Passarini Damiano, Di Gioia Valeria, Sesti Giorgio, Conti Fabrizio, Spinelli Francesca Romana, Corpolongo Angela, Chimenti Maria Sole, Ferraioli Mario, Sebastiani Gian Domenico, Benucci Maurizio, Li Gobbi Francesca, Santoro Anna Paola, Capri Andrea, Puro Vincenzo, Nicastri Emanuele, Goletti Delia

机构信息

Department of Clinical and Molecular Medicine, "Sapienza" University, S. Andrea University Hospital, 00189 Rome, Italy.

Epidemiology Department, National Institute for Infectious Diseases Lazzaro Spallanzani-Istituto di Ricovero e Cura a Carattere Scientifico (IRCCS), 00149 Rome, Italy.

出版信息

Vaccines (Basel). 2023 Nov 2;11(11):1684. doi: 10.3390/vaccines11111684.

Abstract

: We aimed to analyse the incidence and severity of breakthrough infections (BIs) in rheumatoid arthritis (RA) patients after a COronaVIrus Disease 2019 (COVID-19) vaccination booster dose. : We enrolled 194 RA patients and 1002 healthcare workers (HCWs) as controls. Clinical, lifestyle and demographic factors were collected at the time of the third dose, and immunogenicity analyses were carried out in a subgroup of patients at 4-6 weeks after the third dose. BIs were experienced by 42% patients (82/194) with a median time since the last vaccination of 176 days. Older age (>50 years; aHR 0.38, 95% CI: 0.20-0.74), receiving conventional synthetic disease modifying antirheumatic drugs (csDMARDs) (aHR 0.52, 95%CI: 0.30-0.90) and having a titre of neutralising antibodies >20 (aHR 0.36, 95% CI: 0.12-1.07) were identified as protective factors. Conversely, anti-IL6R treatment and anti-CD20 therapy increased BI probability. BIs were mostly pauci-symptomatic, but the hospitalisation incidence was significantly higher than in HCWs (8.5% vs. 0.19%); the main risk factor was anti-CD20 therapy. Being older than 50 years and receiving csDMARDs were shown to be protective factors for BI, whereas anti-IL6R or anti-CD20 therapy increased the risk. Higher neutralising antibody titres were associated with a lower probability of BI. If confirmed in a larger population, the identification of a protective cut-off would allow a personalised risk-benefit therapeutic management of RA patients.

摘要

我们旨在分析2019冠状病毒病(COVID-19)加强疫苗接种后类风湿关节炎(RA)患者突破性感染(BI)的发生率和严重程度。我们招募了194例RA患者和1002名医护人员(HCW)作为对照。在接种第三剂疫苗时收集临床、生活方式和人口统计学因素,并在第三剂疫苗接种后4至6周对部分患者进行免疫原性分析。42%的患者(82/194)发生了BI,自上次接种以来的中位时间为176天。年龄较大(>50岁;调整后风险比[aHR]0.38,95%置信区间[CI]:0.20-0.74)、接受传统合成改善病情抗风湿药物(csDMARDs)治疗(aHR 0.52,95%CI:0.30-0.90)以及中和抗体滴度>20(aHR 0.36,95%CI:0.12-1.07)被确定为保护因素。相反,抗IL6R治疗和抗CD20治疗会增加BI的可能性。BI大多症状轻微,但住院发生率显著高于医护人员(8.5%对0.19%);主要风险因素是抗CD20治疗。年龄大于50岁和接受csDMARDs治疗被证明是BI的保护因素,而抗IL6R或抗CD20治疗会增加风险。较高的中和抗体滴度与较低的BI可能性相关。如果在更大规模人群中得到证实,确定一个保护临界值将有助于对RA患者进行个性化的风险效益治疗管理。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7673/10675674/5a955c4cc7f9/vaccines-11-01684-g001.jpg

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