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补体调节蛋白的表达:CD46、CD55 和 CD59 以及对 CD20+非霍奇金淋巴瘤患者利妥昔单抗的反应。

Expression of complement regulatory proteins: CD46, CD55, and CD59 and response to rituximab in patients with CD20+ non-Hodgkin's lymphoma.

机构信息

Department of Haematology, Blood Neoplasms and Bone Marrow Transplantation, Wroclaw Medical University, Pasteura 4 Street, Wroclaw, 50-367, Poland.

出版信息

Med Oncol. 2010 Sep;27(3):743-6. doi: 10.1007/s12032-009-9278-9. Epub 2009 Aug 7.

Abstract

Rituximab is an anti-CD20 humanized monoclonal antibody widely used in the treatment of B-cell non-Hodgkin's lymphomas (NHLs). Its mechanism of action is related with complement function-complement mediated cytotoxicity. CD46, CD55, and CD59 are complement regulatory proteins. The aim of this study was to analyze expression of complement inhibitors CD46, CD55, and CD59 in patients with CD20(+) NHLs treated with rituximab combined with chemotherapy. A total of 27 patients with CD20(+) NHLs were evaluated (13 females and 14 males). The median age of patients was 56 years. All patients were examined before treatment with rituximab. Expression of CD46, CD55, and CD59 was determined by two-color flow cytometry. A total of 15 patients achieved complete response (CR), 5 patients achieved partial response, and 7 patients had no or minimal response (NR) after rituximab therapy. We observed that expression of CD46 and CD59 were higher in patients with CR than in group with NR. Expression of CD55 and CD59 were higher in patients with bulky disease. In conclusion level of expression of CD46, CD55, and CD59 could be clinically helpful to predict the response to rituximab therapy.

摘要

利妥昔单抗是一种抗 CD20 的人源化单克隆抗体,广泛用于治疗 B 细胞非霍奇金淋巴瘤(NHL)。其作用机制与补体功能有关-补体介导的细胞毒性。CD46、CD55 和 CD59 是补体调节蛋白。本研究旨在分析接受利妥昔单抗联合化疗治疗的 CD20(+)NHL 患者中补体抑制剂 CD46、CD55 和 CD59 的表达。共评估了 27 例 CD20(+)NHL 患者(13 名女性和 14 名男性)。患者的中位年龄为 56 岁。所有患者在接受利妥昔单抗治疗前均接受检查。通过双色流式细胞术测定 CD46、CD55 和 CD59 的表达。利妥昔单抗治疗后,15 例患者达到完全缓解(CR),5 例患者达到部分缓解,7 例患者无缓解或最小缓解(NR)。我们观察到 CR 患者的 CD46 和 CD59 表达高于 NR 组。大肿块疾病患者的 CD55 和 CD59 表达较高。总之,CD46、CD55 和 CD59 的表达水平可能有助于临床预测对利妥昔单抗治疗的反应。

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