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Serum Gelatinases Levels in Multiple Sclerosis Patients during 21 Months of Natalizumab Therapy

机译:纳他珠单抗治疗21个月期间多发性硬化症患者的血清明胶酶水平

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摘要

Background. Natalizumab is a highly effective treatment approved for multiple sclerosis (MS). The opening of the blood-brain barrier mediated by matrix metalloproteinases (MMPs) is considered a crucial step in MS pathogenesis. Our goal was to verify the utility of serum levels of active MMP-2 and MMP-9 as biomarkers in twenty MS patients treated with Natalizumab. Methods. Serum levels of active MMP-2 and MMP-9 and of specific tissue inhibitors TIMP-1 and TIMP-2 were determined before treatment and for 21 months of therapy. Results. Serum levels of active MMP-2 and MMP-9 and of TIMP-1 and TIMP-2 did not differ during the treatment. The ratio between MMP-9 and MMP-2 was increased at the 15th month compared with the 3rd, 6th, and 9th months, greater at the 18th month than at the 3rd and 6th months, and higher at the 21st than at the 3rd and 6th months. Discussion. Our data indicate that an imbalance between active MMP-9 and active MMP-2 can occur in MS patients after 15 months of Natalizumab therapy; however, they do not support the use of serum active MMP-2 and active MMP-9 and TIMP-1 and TIMP-2 levels as biomarkers for monitoring therapeutic response to Natalizumab.
机译:背景。纳他珠单抗是一种批准用于多发性硬化症(MS)的高效治疗方法。基质金属蛋白酶(MMPs)介导的血脑屏障的开放被认为是MS发病机理中的关键步骤。我们的目标是验证活性NMP-2和MMP-9的血清水平在纳他珠单抗治疗的20名MS患者中作为生物标志物的作用。方法。在治疗前和治疗21个月时测定了活性MMP-2和MMP-9以及特定组织抑制剂TIMP-1和TIMP-2的血清水平。结果。在治疗期间,血清中活性MMP-2和MMP-9以及TIMP-1和TIMP-2的水平没有差异。与第3、6和9个月相比,第15个月MMP-9和MMP-2之间的比率有所增加,第18个月的MMP-9和MMP-2的比率大于第3和第6个月,而第21个月的MMP-9和MMP-2的比率高于第3和第6个月。第六个月讨论。我们的数据表明,那他珠单抗治疗15个月后,MS患者中可能发生活跃MMP-9和活跃MMP-2之间的失衡。但是,他们不支持使用血清活性MMP-2和活性MMP-9和TIMP-1和TIMP-2水平作为生物标记物来监测对那他珠单抗的治疗反应。

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