接受纳他珠单抗治疗的多发性硬化症患者接种 Ad26.COV2.S 疫苗后的体液免疫反应

M. Gudesblatt, Myassar Zarif, Barbara Bumstead, M. Buhse, Olivia Kaczmarek, Hanyue Li, Zhaonan Sun, Nicole Scott, Jason P Mendoza, Robin L Avila
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引用次数: 0

摘要

多发性硬化疾病修饰疗法的免疫调节作用可能影响对严重急性呼吸综合征冠状病毒疫苗的免疫反应2。我们分析了Ad26.COV2前后的严重急性呼吸综合征冠状病毒2特异性抗体反应和淋巴细胞谱。S (Johnson & Johnson)在接受natalizumab治疗的多发性硬化患者中的疫苗接种。接种疫苗后4周,抗严重急性呼吸综合征冠状病毒2尖峰免疫球蛋白G平均水平增加72倍,6个月后增加137倍。其他免疫信号在正常范围内。接受natalizumab治疗的多发性硬化症患者对Ad26.COV2具有强大的免疫应答。S疫苗等免疫信号未受明显影响。
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Humoral immune response after Ad26.COV2.S vaccination in patients with multiple sclerosis treated with natalizumab
The immunomodulatory effects of disease-modifying therapies for multiple sclerosis might affect the immune response to vaccines for severe acute respiratory syndrome coronavirus 2. We analyzed the severe acute respiratory syndrome coronavirus 2-specific antibody response and lymphocyte profile before and after Ad26.COV2.S (Johnson & Johnson) vaccination in natalizumab-treated patients with multiple sclerosis. There was a 72-fold increase in mean anti-severe acute respiratory syndrome coronavirus 2 spike immunoglobulin G levels 4 weeks after vaccination and a 137-fold increase after 6 months. Other immune signals were within normal ranges. Natalizumab-treated patients with multiple sclerosis had a robust immune response to Ad26.COV2.S vaccine, and other immune signals were not significantly affected.
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来源期刊
CiteScore
4.70
自引率
0.00%
发文量
54
审稿时长
15 weeks
期刊最新文献
Fatigue in multiple sclerosis: A scoping review of pharmacological and nonpharmacological interventions. Early comorbidities and diagnostic challenges in people with multiple sclerosis with possible impact on disease management. Validation of the Swedish Multiple Sclerosis registry for pediatric-onset multiple sclerosis. Diagnostic challenges in SLIPPERS syndrome: Case report. Disproportional smaller fornix with altered microstructure in pediatric multiple sclerosis shown by high-resolution fluid-suppressed diffusion tractography.
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