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体液对 COVID-19 疫苗的反应取决于类风湿关节炎患者利妥昔单抗的剂量和时间。

Humoral response to coronavirus disease-19 vaccines is dependent on dosage and timing of rituximab in patients with rheumatoid arthritis.

机构信息

Radboud Institute for Health Sciences, Department of Rheumatology, Radboud University Medical Center, Nijmegen.

Department of Rheumatology, Sint Maartenskliniek, Ubbergen.

出版信息

Rheumatology (Oxford). 2022 Jun 28;61(SI2):SI175-SI179. doi: 10.1093/rheumatology/keac206.

Abstract

OBJECTIVES

Humoral response to vaccines in RA patients treated with rituximab (RTX) in standard dosages (≥1000 mg) is decreased. Ultra-low dosages (500 or 200 mg) may have better response. Also, timing after latest RTX infusion may be an important variable. We aimed to investigate the influence of RTX dosage and timing on response to COVID-19 vaccination in RA patients.

METHODS

A single-centre observational study (n = 196) investigated the humoral response, measured by total Ig anti-COVID-19 assay (positive response ≥1.1), 2-6 weeks after complete COVID-19 vaccination. A multivariable logistic regression model was built to study the effect of RTX dosage and time between latest rituximab and vaccination on response, adjusting for age and methotrexate use.

RESULTS

After two-dose vaccination, the response rate was significantly better for patients receiving 200 mg (n = 31, 45%) rituximab compared with 1000 mg (n = 98, 26%; odds ratio 3.07, 95% CI 1.14-8.27) and for each additional month between latest rituximab and vaccination (OR 1.67, 1.39-2.01).

CONCLUSION

Both increased time between latest rituximab infusion and complete vaccination, and 200 mg as latest dose were associated with a better response to COVID-19 vaccination and should be considered when trying to increase vaccine response after rituximab in RA patients.

TRIAL REGISTRATION

Netherlands Trial Register, https://www.trialregister.nl/, NL9342.

摘要

目的

在标准剂量(≥1000mg)下接受利妥昔单抗(RTX)治疗的 RA 患者对疫苗的体液反应降低。超低剂量(500 或 200mg)可能具有更好的反应。此外,RTX 输注后最新时间可能是一个重要的变量。我们旨在研究 RTX 剂量和时间对 RA 患者 COVID-19 疫苗接种反应的影响。

方法

一项单中心观察性研究(n=196)调查了 COVID-19 完全接种后 2-6 周通过总 Ig 抗 COVID-19 测定(阳性反应≥1.1)测量的体液反应。建立多变量逻辑回归模型,研究 RTX 剂量和最近利妥昔单抗与疫苗接种之间的时间对反应的影响,调整年龄和甲氨蝶呤的使用。

结果

接受 200mg(n=31)RTX 的患者在两剂疫苗接种后的反应率明显优于接受 1000mg(n=98)RTX 的患者(26%比 45%;比值比 3.07,95%CI 1.14-8.27),并且最近利妥昔单抗与疫苗接种之间的时间每增加一个月(OR 1.67,1.39-2.01)。

结论

增加最近利妥昔单抗输注与完全接种疫苗之间的时间,以及将 200mg 作为最后一剂剂量与 COVID-19 疫苗接种的更好反应相关,在尝试增加 RA 患者利妥昔单抗后的疫苗反应时应考虑这一点。

试验注册

荷兰试验注册处,https://www.trialregister.nl/,NL9342。

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