Department of Neurology and Institute of Experimental Neurology, Università Vita-Salute San Raffaele, Ospedale San Raffaele, Milan, Italy.
Rutgers, The State University of New Jersey, New Jersey Medical School, Department of Neurology & Neurosciences, Medical Science Building, 185 South Orange Avenue, MSB, H506, Newark, NJ 07101-1709, United States.
Mult Scler Relat Disord. 2019 Apr;29:168-174. doi: 10.1016/j.msard.2019.01.038. Epub 2019 Jan 24.
Immune reconstitution therapies (IRT) for patients with multiple sclerosis are used for short, intermittent treatment periods to induce immune resetting and allow subsequent treatment-free periods. Cladribine tablets are postulated to be an IRT that causes selective and transient reductions in CD19 B cells and T cells, followed by reconstitution of adaptive immune function.
To characterize long-term lymphocyte count changes in pooled data from the 2-year CLARITY and subsequent 2-year CLARITY Extension studies, and the PREMIERE registry (Long-term CLARITY cohort).
Data from patients randomized to placebo (n = 435) or cladribine tablets 10 mg (MAVENCLAD; 3.5 mg/kg cumulative dose over 2 years, referred to as cladribine tablets 3.5 mg/kg; n = 685) in CLARITY or CLARITY Extension, including time spent in the PREMIERE registry were pooled to provide long-term follow-up data. The study investigated absolute lymphocyte counts (ALC) up to 312 weeks and B and T cell subsets up to 240 weeks after the first dose, in patients receiving placebo or cladribine tablets 3.5 mg/kg administered as two short (4 or 5 days) weekly treatments at the start of months 1 and 2 in each treatment year, followed by no further active treatment.
Treatment with cladribine tablets 3.5 mg/kg resulted in selective reductions in B and T lymphocytes. Lymphocyte recovery began soon after treatment in each of years 1 and 2. Median ALC recovered to the normal range and CD19 B cells recovered to threshold values by week 84, approximately 30 weeks after the last dose of cladribine tablets in year 2. Median CD4 T cell counts recovered to threshold values by week 96 (approximately 43 weeks after the last dose of cladribine tablets in year 2). Median CD8 cell counts never dropped below the threshold value.
These results show the dynamics of lymphocyte count changes following treatment with cladribine tablets 3.5 mg/kg. The immune cell repopulation results provide further evidence that cladribine tablets may represent a form of IRT.
免疫重建疗法(IRT)用于多发性硬化症患者的短期间歇性治疗,以诱导免疫重置并允许随后的无治疗期。克拉屈滨片被认为是一种 IRT,可导致 CD19 B 细胞和 T 细胞选择性和短暂减少,随后适应性免疫功能重建。
从 CLARITY 研究的 2 年和随后的 CLARITY 扩展研究以及 PREMIERE 登记处(长期 CLARITY 队列)的合并数据中描述淋巴细胞计数的长期变化。
将随机分配至安慰剂(n=435)或克拉屈滨片 10mg(MAVENCLAD;2 年内累积剂量 3.5mg/kg,简称克拉屈滨片 3.5mg/kg;n=685)的患者的数据进行合并,以提供长期随访数据。该研究调查了接受安慰剂或克拉屈滨片 3.5mg/kg 治疗的患者在接受第一个剂量后长达 312 周的绝对淋巴细胞计数(ALC)以及 B 和 T 细胞亚群,克拉屈滨片 3.5mg/kg 每 2 年的第 1 和第 2 个月的第 1 周和第 2 周进行两次短期(4 或 5 天)每周治疗,随后不再进行主动治疗。
克拉屈滨片 3.5mg/kg 治疗导致 B 和 T 淋巴细胞选择性减少。在每个治疗年度的第 1 年和第 2 年的治疗后不久,淋巴细胞开始恢复。中位 ALC 在第 2 年的第 84 周(第 2 年最后一剂克拉屈滨片后约 30 周)恢复至正常范围,CD19 B 细胞恢复至阈值。中位 CD4 T 细胞计数在第 96 周(第 2 年最后一剂克拉屈滨片后约 43 周)恢复至阈值。中位 CD8 细胞计数从未低于阈值。
这些结果显示了克拉屈滨片 3.5mg/kg 治疗后淋巴细胞计数变化的动态。免疫细胞再增殖结果进一步证明,克拉屈滨片可能代表一种 IRT。