Division of Rheumatology, Inflammation, and Immunity, Brigham and Women's Hospital, Boston, MA, USA.
Division of Rheumatology, Allergy, and Immunology, Massachusetts General Hospital, Boston, MA, USA; Rheumatology and Allergy Clinical Epidemiology Research Center, Mongan Institute, Department of Medicine, Massachusetts General Hospital, Boston, MA, USA.
Lancet Rheumatol. 2024 Jan;6(1):e21-e30. doi: 10.1016/S2665-9913(23)00272-2. Epub 2023 Nov 15.
Patients with systemic autoimmune rheumatic diseases using disease-modifying antirheumatic drugs (DMARDs) might have blunted responses to COVID-19 vaccines. The initial mRNA vaccine series is defined as three doses for this population and a fourth booster dose is recommended. The effectiveness of the fourth dose in patients with systemic autoimmune rheumatic diseases using DMARDs is not well established. We aimed to assess the effectiveness of receiving versus not receiving a fourth dose of COVID-19 mRNA vaccine using a target trial framework, in a cohort of patients with systemic autoimmune rheumatic diseases receiving DMARD therapy.
We conducted an emulated target trial using observational data from the Mass General Brigham health-care system to compare receiving versus not receiving a fourth mRNA vaccine dose. Analysed patients had systemic autoimmune rheumatic diseases, were prescribed DMARDs, and were eligible for a fourth dose of BNT162b2 or mRNA-1273 vaccines between Jan 16 and June 11, 2022. To account for temporal changes, the study period was divided into 1-week intervals. Fourth-dose-exposed patients were included in a 1-week interval if they received a fourth mRNA dose in that interval; fourth-dose-unexposed patients were eligible for but had not received the fourth dose of the vaccine. The primary outcome was a SARS-CoV-2 infection; the secondary outcome was severe SARS-CoV-2 infection (ie, admission to hospital or death within -3 to +14 days of a positive test). We assessed the effectiveness of the fourth dose using time-stratified, overlap propensity score-weighted Cox regression models.
We included 4305 patients, 3126 of whom received a fourth dose of vaccine and 1179 who had not. The median follow-up time was 135 days (IQR 112-154) among patients who had received a fourth dose and 65 days (30-156) among patients who had not received a fourth dose. After overlap weighting in both groups, 1863 (72·7%) of 2563 participants were women, 700 (27·3%) were men, and 2242 (87·5%) were White. Rheumatoid arthritis was present in 1392 (54·3%) of 2563 participants; the most frequent treatments were conventional synthetic DMARDs (1489 [58·1%]) or biological DMARDs (1007 [39·3%]). SARS-CoV-2 infection risk was lower among patients receiving versus not receiving a fourth dose of vaccine (HR 0·59 [95% CI 0·47-0·74]). A fourth dose reduced the risk of admission to hospital or death within -3 to +14 days of SARS-CoV-2 infection (0·35 [0·14-0·85]).
In this emulated target trial, a fourth dose of COVID-19 mRNA vaccine reduced the risk of SARS-CoV-2 infection and severe COVID-19 among patients with systemic autoimmune rheumatic diseases using DMARDs during the Omicron era. Patients with systemic autoimmune rheumatic diseases should be encouraged to remain up-to-date with COVID-19 vaccinations.
The National Institutes of Health and the National Institute of Arthritis and Musculoskeletal and Skin Diseases.
使用疾病修饰抗风湿药物(DMARDs)的系统性自身免疫性风湿病患者对 COVID-19 疫苗的反应可能减弱。对于这一人群,初始 mRNA 疫苗系列定义为三剂,建议接种第四剂加强针。使用 DMARDs 的系统性自身免疫性风湿病患者接种第四剂疫苗的有效性尚未得到充分证实。我们旨在使用目标试验框架评估接受与不接受 COVID-19 mRNA 疫苗第四剂的有效性,在接受 DMARD 治疗的系统性自身免疫性风湿病患者队列中进行评估。
我们利用来自马萨诸塞州综合医院保健系统的观察性数据进行了模拟目标试验,以比较接受与不接受第四剂 COVID-19 mRNA 疫苗。分析的患者患有系统性自身免疫性疾病,接受 DMARD 治疗,并且在 2022 年 1 月 16 日至 6 月 11 日期间有资格接种 BNT162b2 或 mRNA-1273 疫苗的第四剂。为了考虑到时间变化,研究期间分为 1 周间隔。如果第四剂暴露组患者在该间隔内接受了第四剂 mRNA 疫苗,则将其纳入 1 周间隔;第四剂未暴露组患者有资格但尚未接种第四剂疫苗。主要结局是 SARS-CoV-2 感染;次要结局是严重 SARS-CoV-2 感染(即,在阳性检测后的 -3 至 +14 天内住院或死亡)。我们使用时间分层、重叠倾向评分加权 Cox 回归模型评估第四剂的有效性。
我们纳入了 4305 名患者,其中 3126 名患者接种了第四剂疫苗,1179 名患者未接种。在接种第四剂的患者中,中位随访时间为 135 天(IQR 112-154),未接种第四剂的患者为 65 天(30-156)。在两组重叠加权后,2563 名参与者中有 1863 名(72.7%)为女性,700 名(27.3%)为男性,2242 名(87.5%)为白人。2563 名参与者中有 1392 名(54.3%)患有类风湿关节炎;最常见的治疗方法是常规合成 DMARDs(1489 名[58.1%])或生物 DMARDs(1007 名[39.3%])。与未接种第四剂疫苗的患者相比,接种第四剂疫苗的患者 SARS-CoV-2 感染风险较低(HR 0.59 [95%CI 0.47-0.74])。第四剂疫苗降低了 SARS-CoV-2 感染后 -3 至 +14 天内住院或死亡的风险(0.35 [0.14-0.85])。
在这项模拟目标试验中,在 Omicron 时代,使用 DMARDs 的系统性自身免疫性风湿病患者接种第四剂 COVID-19 mRNA 疫苗降低了 SARS-CoV-2 感染和严重 COVID-19 的风险。应鼓励患有系统性自身免疫性风湿病的患者及时接种 COVID-19 疫苗。
美国国立卫生研究院和国家关节炎和肌肉骨骼及皮肤病研究所。