Department of Rheumatology, Radboud Institute for Health Sciences, Radboud University Medical Center, Nijmegen, The Netherlands.
Department of Rheumatology, Sint Maartenskliniek, Ubbergen, The Netherlands.
Rheumatology (Oxford). 2023 Apr 3;62(4):1627-1630. doi: 10.1093/rheumatology/keac486.
In patients with RA treated with (ultra-)low-dose rituximab (RTX), we investigated the association of dosing and timing of RTX on seroconversion after a third coronavirus disease 2019 (COVID-19) vaccination and the persistence of humoral response after a two-dose vaccination.
In this monocentre observational study, patients from the COVAC cohort were included in the third vaccine analysis if humoral response was obtained 2-6 weeks after a third vaccination in previous non-responders and in the persistence analysis if a follow-up humoral response was obtained before a third vaccination in previous responders. Dichotomization between positive and negative response was based on the assay cut-off. The association between the latest RTX dose before first vaccination, timing between the latest RTX dose and vaccination and response was analysed with univariable logistic regression.
Of the 196 patients in the cohort, 98 were included in the third vaccine analysis and 23 in the persistence analysis. Third vaccination response was 19/98 (19%) and was higher for 200 mg RTX users [5/13 (38%)] than for 500 and 1000 mg users [7/37 (19%) and 7/48 (15%), respectively]. Non-significant trends were seen for higher response with lower dosing [200 vs 1000 mg: odds ratio (OR) 3.66 (95% CI 0.93, 14.0)] and later timing [per month since infusion: OR 1.16 (95% CI 0.97, 1.35)]. Humoral response persisted in 96% (22/23) and 89% (8/9) of patients who received RTX between the two measurements.
Repeated vaccination as late as possible after the lowest RTX dose possible seems the best vaccination strategy. A once positive humoral response after COVID-19 vaccination persists irrespective of intercurrent RTX infusion. Study registration. Netherlands Trial Registry (https://www.trialregister.nl/), NL9342.
在接受(超低)剂量利妥昔单抗(RTX)治疗的类风湿关节炎(RA)患者中,我们研究了 RTX 给药剂量和时间与第三次新型冠状病毒病 2019(COVID-19)疫苗接种后的血清转换以及两剂疫苗接种后的体液反应持续时间之间的关系。
在这项单中心观察性研究中,如果以前的无反应者在第三次接种疫苗后 2-6 周获得了体液反应,则将 COVAC 队列中的患者纳入第三次疫苗分析,如果以前的反应者在第三次接种疫苗前获得了随访的体液反应,则将其纳入持续性分析。基于检测限,将阳性和阴性反应进行二分法。使用单变量逻辑回归分析首次接种前最近一次 RTX 剂量、RTX 剂量与接种时间之间的关系与反应之间的关系。
在队列中的 196 名患者中,98 名被纳入第三次疫苗分析,23 名被纳入持续性分析。第三次接种疫苗的反应率为 19/98(19%),200mg RTX 使用者的反应率更高[5/13(38%)],而 500mg 和 1000mg 使用者的反应率分别为 7/37(19%)和 7/48(15%)。剂量越低,反应越高[200 与 1000mg:比值比(OR)3.66(95%CI 0.93,14.0)]和时间越晚[每输注一个月:OR 1.16(95%CI 0.97,1.35)],这一趋势无统计学意义。在接受 RTX 治疗的 23 名患者中,有 96%(22/23)和 89%(8/9)的患者的体液反应持续存在。
尽可能晚地在尽可能低的 RTX 剂量后重复接种疫苗似乎是最好的疫苗接种策略。COVID-19 疫苗接种后一旦出现阳性体液反应,无论是否有 RTX 输注,其反应均持续存在。研究注册:荷兰试验注册中心(https://www.trialregister.nl/),NL9342。