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作 者:刘先桃[1]
出 处:《内蒙古医学杂志》2014年第10期1189-1191,共3页Inner Mongolia Medical Journal
摘 要:目的 探讨小剂量利妥昔单抗治疗复发难治性免疫性血小板减少症(ITP)的疗效、安全性及治疗前后B细胞、血小板膜糖蛋白特异性自身抗体的变化.方法 利妥昔单抗100mg静脉滴注,每周1次,连用4周,治疗23例复发难治性ITP患者,无使用免疫抑制剂、化疗药、抗凝药及激素冲击疗法.监测治疗前后的血常规,血清免疫球蛋白(IgG、IgM、IgA),血小板膜糖蛋白抗体及CD3+、CD4+、CD8+、CD19+、CD20+细胞数.结果 9例完全有效,5例有效,9例无效.中位疗效持续时间8(5~23)个月,有效患者有中3例复发,其余均维持较好.有效患者治疗后血小板自身抗体均转阴.治疗前后外周血血红蛋白、白细胞计数无明显变化,血清IgG、IgM、IgA无明显变化,CD3+、CD4+、CD8+细胞数无明显变化.治疗后CDI9+/CD20+细胞明显下降.多数患者耐受好.结论 小剂量利妥昔单抗治疗复发难治性ITP疗效肯定,不良反应可以耐受.Objective To evaluate the efficacy and safety of rituximab on B- lymphocytes and anti - platelet glycoprotein- specific antibodies in patients with refractory primary immune thrombocytopenic(ITP). Methods 23 ITP patients with a median age of 36 years(range 1 6 - 56years)received solely intravenous rituximab at the dose of 100mg once weekly for consecutive 4 weeks. Lab studies included complete blood count, serum concentrations of IgG, IgM and IgA. CD3 +, CD4 +, CD8 +, CD19 + and CD20 + cell numbers were assayed by flow cytometry and anti- platelet glycoprotein- specific antibodies(GPⅡb/m a, GP Ⅰb/Ⅸ)were assayed by monolonal antibody- specific immobilisation of platelet antigens(MAIPA)prior to and following ritux- imab therapy. The response was evaluated according to the response criteria of international working group of ITP. Results Complete responses were achieved in 9 cases. Response in 5 cases, and no response in 9 cases. Responses were sustained 5 to 23 months(median 8 months)with 3 cases relapsed. After 4 weeks of rituximab therapy, GPU b/Ⅲ a and GP Ⅰb/Ⅺ disappeared in responded patients, and CD 19 +/CD20 + cells were almost depleted in all patients. As expected, the serum concentrations of IgG, IgM, IgA, and the T cell counts were not changedAfter therapy. Three patients developed infusion - related reaction. Conclusion Rituximab is effective and safe, and the adverse reaction is tolerable.
分 类 号:R554.6[医药卫生—血液循环系统疾病]
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