Center of Clinical Neuroscience, Department of Neurology, University Hospital Carl Gustav Carus Dresden, Technical University of Dresden, Dresden, Germany.
Front Immunol. 2022 Jul 25;13:897748. doi: 10.3389/fimmu.2022.897748. eCollection 2022.
Sphingosine-1-phosphate receptor modulators and anti-CD20 treatment are widely used disease-modifying treatments for multiple sclerosis. Unfortunately, they may impair the patient's ability to mount sufficient humoral and T-cellular responses to vaccination, which is of special relevance in the context of the SARS-CoV-2 pandemic. We present here a case series of six multiple sclerosis patients on treatment with sphingosine-1-phosphate receptor modulators who failed to develop SARS-CoV-2-specific antibodies and T-cells after three doses of vaccination. Due to their ongoing immunotherapy, lacking vaccination response, and additional risk factors, we offered them pre-exposure prophylactic treatment with monoclonal SARS-CoV-2-neutralizing antibodies. Initially, treatment was conducted with the antibody cocktail casirivimab/imdevimab. When the SARS-CoV-2 Omicron variant became predominant, we switched treatment to monoclonal antibody sotrovimab due to its sustained neutralizing ability also against the Omicron strain. Since sotrovimab was approved only for the treatment of COVID-19 infection and not for pre-exposure prophylaxis, we switched treatment to tixagevimab/cilgavimab as soon as it was granted marketing authorization in the European Union. This antibody cocktail has retained, albeit reduced, neutralizing activity against the Omicron variant and is approved for pre-exposure prophylaxis. No severe adverse events were recorded for our patients. One patient had a positive RT-PCR for SARS-CoV-2 under treatment with sotrovimab, but was asymptomatic. The other five patients did not develop symptoms of an upper respiratory tract infection or evidence of a SARS-CoV-2 infection during the time of treatment up until the finalization of this report. SARS-CoV-2-neutralizing antibody treatment should be considered individually for multiple sclerosis patients lacking adequate vaccination responses on account of their immunomodulatory treatment, especially in times of high incidences of SARS-CoV-2 infection.
鞘氨醇-1-磷酸受体调节剂和抗 CD20 治疗被广泛用于多发性硬化症的疾病修饰治疗。不幸的是,它们可能会损害患者对疫苗产生足够体液和 T 细胞反应的能力,这在 SARS-CoV-2 大流行的背景下尤为重要。我们在这里报告了 6 例正在接受鞘氨醇-1-磷酸受体调节剂治疗的多发性硬化症患者的病例系列,他们在接种三剂疫苗后未能产生 SARS-CoV-2 特异性抗体和 T 细胞。由于他们正在进行免疫治疗、缺乏疫苗反应和其他危险因素,我们为他们提供了单克隆 SARS-CoV-2 中和抗体的暴露前预防性治疗。最初,我们使用抗体鸡尾酒 casirivimab/imdevimab 进行治疗。当 SARS-CoV-2 的奥密克戎变体成为主要流行株时,由于其对奥密克戎株的持续中和能力,我们切换为治疗用单克隆抗体 sotrovimab。由于 sotrovimab 仅被批准用于 COVID-19 感染的治疗,而不是用于暴露前预防,因此一旦在欧盟获得上市许可,我们就切换为 tixagevimab/cilgavimab 进行治疗。这种抗体鸡尾酒对奥密克戎变体仍保留了(尽管有所降低)中和活性,并且已被批准用于暴露前预防。我们的患者未记录到严重的不良事件。一名患者在接受 sotrovimab 治疗时 SARS-CoV-2 的 RT-PCR 检测呈阳性,但无症状。在接受治疗期间直至本报告定稿时,其他五名患者未出现上呼吸道感染症状或 SARS-CoV-2 感染的证据。对于缺乏足够疫苗反应的多发性硬化症患者,由于其免疫调节治疗,应单独考虑 SARS-CoV-2 中和抗体治疗,尤其是在 SARS-CoV-2 感染发生率较高的情况下。