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首页> 外文期刊>Neurology. >Humoral- and T-Cell-Specific Immune Responses to SARS-CoV-2 mRNA Vaccination in Patients With MS Using Different Disease-Modifying Therapies
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Humoral- and T-Cell-Specific Immune Responses to SARS-CoV-2 mRNA Vaccination in Patients With MS Using Different Disease-Modifying Therapies

机译:体液和T-Cell-Specific免疫反应SARS-CoV-2 mRNA在MS患者进行疫苗接种使用不同的疾病修饰治疗

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Background and objectives: To evaluate the immune-specific response after full severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) vaccination of patients with multiple sclerosis (MS) treated with different disease-modifying drugs by the detection of both serologic and T-cell responses.Methods: Healthcare workers (HCWs) and patients with MS, having completed the 2-dose schedule of an mRNA-based vaccine against SARS-CoV-2 in the past 2-4 weeks, were enrolled from 2 parallel prospective studies conducted in Rome, Italy, at the National Institute for Infectious diseases Spallanzani-IRCSS and San Camillo Forlanini Hospital. Serologic response was evaluated by quantifying the region-binding domain (RBD) and neutralizing antibodies. Cell-mediated response was analyzed by a whole-blood test quantifying interferon (IFN)-γ response to spike peptides. Cells responding to spike stimulation were identified by fluorescence-activated cell sorting analysis.Results: We prospectively enrolled 186 vaccinated individuals: 78 HCWs and 108 patients with MS. Twenty-eight patients with MS were treated with IFN-β, 35 with fingolimod, 20 with cladribine, and 25 with ocrelizumab. A lower anti-RBD antibody response rate was found in patients treated with ocrelizumab (40%, p < 0.0001) and fingolimod (85.7%, p = 0.0023) compared to HCWs and patients treated with cladribine or IFN-β. Anti-RBD antibody median titer was lower in patients treated with ocrelizumab (p < 0.0001), fingolimod (p < 0.0001), and cladribine (p = 0.010) compared to HCWs and IFN-β-treated patients. Serum neutralizing activity was present in all the HCWs tested and in only a minority of the fingolimod-treated patients (16.6%). T-cell-specific response was detected in the majority of patients with MS (62%), albeit with significantly lower IFN-γ levels compared to HCWs. The lowest frequency of T-cell response was found in fingolimod-treated patients (14.3%). T-cell-specific response correlated with lymphocyte count and anti-RBD antibody titer (ρ = 0.554, p < 0.0001 and ρ = 0.255, p = 0.0078 respectively). IFN-γ T-cell response was mediated by both CD4+ and CD8+ T cells.Discussion: mRNA vaccines induce both humoral and cell-mediated specific immune responses against spike peptides in all HCWs and in the majority of patients with MS. These results carry relevant implications for managing vaccinations, suggesting promoting vaccination in all treated patients with MS.Classification of evidence: This study provides Class III data that SARS-CoV-2 mRNA vaccination induces both humoral and cell-mediated specific immune responses against viral spike proteins in a majority of patients with MS.
机译:背景和目的:评估完整的严重急性后immune-specific响应呼吸系统综合症冠状病毒2 (SARS-CoV-2)疫苗接种的多发性硬化症患者(MS)治疗不同的疾病药物检测的血清学的和t细胞反应。(卫生工作者)和MS患者,已经完成了服用mRNA-based疫苗的计划SARS-CoV-2过去2 - 4周,被录取从2平行进行的前瞻性研究罗马,意大利,国立研究所传染病Spallanzani-IRCSS和圣卡米洛•Forlanini医院。被量化评估region-binding吗域(RBD)和中和抗体。一个细胞介导的反应进行了分析遗传测试量化干扰素(IFN) -γ应对高峰肽。飙升的刺激了fluorescence-activated细胞分类分析。接种疫苗的个体:78卫生工作者和108名患者女士与28例MS患者用干扰素治疗-β,35 fingolimod, 20与ocrelizumab cladribine, 25。anti-RBD抗体反应率被发现ocrelizumab患者(40%,p <0.0001)和fingolimod (85.7%, p = 0.0023)而卫生工作者和患者cladribine或干扰素-β。效价是患者低ocrelizumab (p < 0.0001), fingolimod (p <0.0001), cladribine相比(p = 0.010)卫生工作者和干扰素-β治疗病人。中和活动存在于所有的卫生工作者测试和只有少数的fingolimod-treated病人(16.6%)。T-cell-specific响应中检测出大部分患者(62%),女士虽然显著降低干扰素-γ水平相比卫生工作者。发现在fingolimod-treated病人(14.3%)。T-cell-specific反应与淋巴细胞计数和anti-RBD抗体效价(ρ=0.0001和ρ= 0.554,p < 0.255, p = 0.0078分别)。CD4 +和CD8 + T细胞。疫苗诱导体液和细胞介导具体对钉肽免疫反应在所有的卫生工作者和多数的患者这些结果女士携带相关的影响疫苗管理,建议推广疫苗接种在所有患者治疗证据MS.Classification:这项研究提供SARS-CoV-2 mRNA的第三类数据疫苗接种诱发体液免疫和细胞特异性免疫反应大多数患者的病毒峰值蛋白质女士。

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