Department of Neurology, Tianjin Neurological Institute, Tianjin Medical University General Hospital, China.
Neurology. 2013 Aug 20;81(8):710-3. doi: 10.1212/WNL.0b013e3182a1aac7. Epub 2013 Jul 24.
To determine the effect of a lower dose of rituximab in depleting B lymphocytes, maintaining low B-cell counts, and relapse in patients with neuromyelitis optica (NMO) and NMO spectrum disorders.
We treated 5 Chinese patients with deteriorating NMO and NMO spectrum disorders with a 100-mg IV infusion of rituximab once a week for 3 consecutive weeks, followed by additional infusion of the same dosage depending on circulating B-cell repopulation.
This reduced dosage of rituximab was sufficient to deplete B cells and maintain low B-cell counts. None of the treated patients experienced relapse, and all patients exhibited stabilized or improved neurologic function during the 1-year follow-up period. MRI revealed the absence of new lesions, no enhancement in spinal cord and brain, a significant shrinkage of spinal cord segments, and a reduction/disappearance of previous brain lesions.
A lower dosage of rituximab may be sufficient in depleting B cells, maintaining low B-cell counts, and preventing disease progression in Chinese patients with NMO.
确定较低剂量利妥昔单抗在耗尽 B 淋巴细胞、维持低 B 细胞计数和复发性视神经脊髓炎(NMO)和 NMO 谱系障碍患者中的作用。
我们用每周一次的 100mg 静脉输注利妥昔单抗治疗 5 例中国恶化的 NMO 和 NMO 谱系障碍患者,连续 3 周,然后根据循环 B 细胞再增殖情况输注相同剂量。
这种降低剂量的利妥昔单抗足以耗尽 B 细胞并维持低 B 细胞计数。接受治疗的患者均未出现复发,所有患者在 1 年随访期间神经系统功能稳定或改善。MRI 显示无新病灶,脊髓和脑部无强化,脊髓节段明显缩小,既往脑病灶减少/消失。
在中国 NMO 患者中,较低剂量的利妥昔单抗可能足以耗尽 B 细胞、维持低 B 细胞计数并预防疾病进展。