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三名自身免疫性血细胞减少症患儿接受利妥昔单抗治疗后抗体持续耗竭。

Persistent antibody depletion after rituximab in three children with autoimmune cytopenias.

作者信息

Adeli Mehdi Mohammad G, Eichner Brian H, Thornburg Courtney, Williams Larry

机构信息

Duke University Medical Center, Durham, NC 277710, USA.

出版信息

Pediatr Hematol Oncol. 2009 Nov;26(8):566-72. doi: 10.3109/08880010903271697.

Abstract

We report 3 children who developed persistent antibody depletion and abnormal response to bacteriophage after rituximab treatment for autoimmune cytopenias. Whether these patients have developed immunodeficiency secondary to an underlying disease process, to rituximab, or both, is not understood. Rituximab is an efficacious drug for a number of pediatric conditions. However, some patients who receive the drug have prolonged suppression or absence of B-cell function. Families should be counseled of this possibility prior to therapy. Patients should have baseline measurement of quantitative immunoglobulins and specific antibody levels and should be monitored for long term changes in immune function after rituximab.

摘要

我们报告了3名儿童,他们在接受利妥昔单抗治疗自身免疫性血细胞减少症后出现了持续性抗体耗竭以及对噬菌体的异常反应。目前尚不清楚这些患者是由于潜在疾病过程、利妥昔单抗还是两者兼而有之而继发免疫缺陷。利妥昔单抗是治疗多种儿科疾病的有效药物。然而,一些接受该药物治疗的患者会出现B细胞功能长期受抑或缺失。在治疗前应告知家属这种可能性。患者应在基线时检测定量免疫球蛋白和特异性抗体水平,并在接受利妥昔单抗治疗后长期监测免疫功能的变化。

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