Hospital das Clinicas HCFMUSP, Faculdade de Medicina, Universidade de Sao Paulo, Sao Paulo, Brazil.
Arthritis Care Res (Hoboken). 2022 Apr;74(4):562-571. doi: 10.1002/acr.24824. Epub 2022 Mar 4.
To date, the only study that has assessed the severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2 mRNA) vaccine in systemic lupus erythematosus (SLE) observed a moderate response, but the sample size precluded an accurate analysis of the effect of individual drugs. Therefore, we evaluated the immunogenicity of an inactivated SARS-CoV-2 vaccine (Sinovac-CoronaVac) and the influence of different medications in SLE. Safety was also assessed.
We conducted a prospective controlled study of 232 SARS-CoV-2-naive SLE patients and 58 SARS-CoV-2-naive controls who were vaccinated with 2 doses of Sinovac-CoronaVac with a 28-day interval (day 0/day 28 [D0/D28]). Immunogenicity analysis at D0/D28 and D69 included anti-SARS-CoV-2 S1/S2 IgG seroconversion (SC) and neutralizing antibodies (NAb) positivity. The influence of individual drugs on immune response and safety was assessed.
Patients and controls were well balanced for age (P = 0.771). At D69, SLE patients showed a moderate SC (70.2% versus 98.1%; P < 0.001) and moderate frequency of NAb positivity (61.5% versus 84.6%; P = 0.002), although both frequencies were lower than in controls. Factors associated with lower SC in univariate analysis at D69 were prednisone use (odds ratio [OR] 0.215 [95% confidence interval (95% CI) 0.108-0.427], P < 0.001) and mycophenolate mofetil (MMF) use (OR 0.201 [95% CI 0.107-0.378], P < 0.001), whereas hydroxychloroquine (HCQ) use led to a 2.5 increase in SC (P = 0.011). SLE patients who were receiving HCQ monotherapy had similar SC to controls at D69 (100% versus 98.1%; P = 1.000). In multivariate analysis, prednisone and MMF use were independently associated with lower SC (P < 0.001) and NAb positivity (P < 0.001). Safety analysis revealed no moderate/severe adverse events.
Sinovac-CoronaVac has a moderate immunogenicity in SARS-CoV-2-naive SLE patients with an excellent safety profile. We further demonstrate that HCQ may improve SC, whereas prednisone and MMF had a major deleterious effect in vaccine response, reinforcing the need to investigate the role of temporary MMF withdrawal or a vaccine-booster dose (ClinicalTrials.gov identifier: NCT04754698).
迄今为止,唯一评估系统性红斑狼疮(SLE)中严重急性呼吸综合征冠状病毒 2(SARS-CoV-2 mRNA)疫苗的研究观察到中度反应,但样本量不足以准确分析个体药物的作用。因此,我们评估了灭活的 SARS-CoV-2 疫苗(科兴-CoronaVac)在 SLE 中的免疫原性和不同药物的影响。还评估了安全性。
我们对 232 名 SARS-CoV-2 初治 SLE 患者和 58 名 SARS-CoV-2 初治对照进行了前瞻性对照研究,他们在 28 天间隔(第 0 天/第 28 天[D0/D28])接受了 2 剂科兴-CoronaVac。在 D0/D28 和 D69 时进行抗 SARS-CoV-2 S1/S2 IgG 血清转化率(SC)和中和抗体(NAb)阳性的免疫原性分析。评估了个体药物对免疫反应和安全性的影响。
患者和对照组在年龄上平衡良好(P=0.771)。在 D69 时,SLE 患者表现出中度 SC(70.2%比 98.1%;P<0.001)和中度 NAb 阳性率(61.5%比 84.6%;P=0.002),尽管这两种频率均低于对照组。D69 时单变量分析中与较低 SC 相关的因素包括泼尼松使用(比值比[OR]0.215[95%置信区间(95%CI)0.108-0.427],P<0.001)和吗替麦考酚酯(MMF)使用(OR 0.201[95%CI 0.107-0.378],P<0.001),而羟氯喹(HCQ)使用使 SC 增加 2.5 倍(P=0.011)。接受 HCQ 单药治疗的 SLE 患者在 D69 时的 SC 与对照组相似(100%比 98.1%;P=1.000)。多变量分析显示,泼尼松和 MMF 的使用与较低的 SC(P<0.001)和 NAb 阳性(P<0.001)相关。安全性分析未发现中度/重度不良事件。
科兴-CoronaVac 在 SARS-CoV-2 初治 SLE 患者中具有中度免疫原性,具有良好的安全性。我们进一步证明,HCQ 可能提高 SC,而泼尼松和 MMF 对疫苗反应有重大的有害影响,这强调了有必要研究暂时停用 MMF 或疫苗加强剂量的作用(临床试验标识符:NCT04754698)。