利妥昔单抗剂量减少与神经脊髓炎视网膜频谱障碍急性复发之间的相关性,COVID-19 流行病的教训。

IF 2.9 3区 医学 Q2 CLINICAL NEUROLOGY Multiple sclerosis and related disorders Pub Date : 2024-10-11 DOI:10.1016/j.msard.2024.105940
Fereshteh Ashtari , Roshanak Mehdipour , Mina Asgari , Arshia Ghalamkari
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引用次数: 0

摘要

背景:COVID-19 是一种病毒感染,它导致了 2020 年 3 月的全球大流行。大流行之初,临床医生遇到了免疫抑制治疗如何影响自身免疫性疾病患者感染 COVID-19 病程的难题。神经脊髓炎视网膜谱系障碍是一种由中枢神经系统炎症引起的自身免疫性星形细胞病。预防急性复发的主要治疗方法包括免疫抑制剂。利妥昔单抗(Rituximab)是 NMOSD 维持治疗中一种行之有效的免疫抑制剂。一些报道指出,利妥昔单抗可能会增加 NMOSD 感染 COVID-19 的风险和死亡率。另一方面,减少剂量或延长治疗间隔可能导致 NMOSD 急性复发和永久性残疾:在这项研究中,我们评估了利妥昔单抗剂量与疫情期间 NMOSD 复发率之间的相关性。这是一项观察性研究,研究对象为 171 名患者,其中 55 例血清反应呈阳性。一些患者常规接受全剂量利妥昔单抗治疗(1000 毫克/剂量,每 6 个月),但其他患者在疫情期间接受半剂量治疗(500 毫克/剂量)。此外,根据 CD19 和 CD20 的水平,一些剂量的处方被延迟:皮尔逊相关系数(r)显示,在血清反应阳性组中,用药量与复发次数呈显著负相关(r:-0.19,p:0.022),因此低用药量与更多急性复发有关。在血清阴性病例中,两者之间没有任何有价值的关系。(P:0.367):结论:降低利妥昔单抗的剂量,尤其是在血清反应阳性的 NMOSD 患者中,有可能导致急性复发。因此,应考虑更频繁地评估 CD19、CD20 和 CD27 水平以及患者的总体临床状况。
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The correlation between rituximab dose reduction and acute relapses of neuromyelitis optica spectrum disorder, lessons from COVID-19 epidemic

Background

COVID-19 was a viral infection that led to a global pandemic in March 2020. At the beginning of the pandemic, clinicians encountered the challenge of how immunosuppressive treatments would affect the course of COVID-19 infection in people with autoimmune diseases. Neuromyelitis optica spectrum disorder is an autoimmune astrocytopathy that is caused by an inflammation in the CNS. Major treatments to prevent acute relapses include immunosuppressive drugs. Rituximab is a well-established immunosuppressive agent in NMOSD maintenance therapy. Some reports suggested that treatment with Rituximab might increase the risk of COVID-19 infection and its mortality in NMOSD. On the other hand, dose reduction or extended interval treatment might lead to acute relapses of NMOSD and permanent disability.

Methods

In this study, we evaluated the correlation between the dose of rituximab and the relapse rate of NMOSD during an epidemic. This was an observational study on 171 patients among whom 55 cases were seropositive. Some patients received full dose rituximab routinely (1000 mg/dose, every 6 months), but others were treated with half dose (500 mg/dose) during the epidemic. Also, some doses were prescribed with a delay, based on the level of CD19 and CD20.

Results

The Pearson correlation coefficient (r) showed a negative and significant relation (r: - 0.19, p: 0.022) between the amount of drug and the number of relapses in the seropositive group, so low dosage of the drug was related to more acute relapses. In seronegative cases, there was not any valuable relationship. (p: 0.367).

Conclusion

Lower dose of rituximab, especially in seropositive NMOSD patients, can potentially lead to acute relapses. So, the more frequent evaluation of the CD19, CD20, and, CD27 levels, and the general clinical condition of the patients should be considered.
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来源期刊
CiteScore
5.80
自引率
20.00%
发文量
814
审稿时长
66 days
期刊介绍: Multiple Sclerosis is an area of ever expanding research and escalating publications. Multiple Sclerosis and Related Disorders is a wide ranging international journal supported by key researchers from all neuroscience domains that focus on MS and associated disease of the central nervous system. The primary aim of this new journal is the rapid publication of high quality original research in the field. Important secondary aims will be timely updates and editorials on important scientific and clinical care advances, controversies in the field, and invited opinion articles from current thought leaders on topical issues. One section of the journal will focus on teaching, written to enhance the practice of community and academic neurologists involved in the care of MS patients. Summaries of key articles written for a lay audience will be provided as an on-line resource. A team of four chief editors is supported by leading section editors who will commission and appraise original and review articles concerning: clinical neurology, neuroimaging, neuropathology, neuroepidemiology, therapeutics, genetics / transcriptomics, experimental models, neuroimmunology, biomarkers, neuropsychology, neurorehabilitation, measurement scales, teaching, neuroethics and lay communication.
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