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The CXCR4 antagonist plerixafor enhances the effect of rituximab in diffuse large B-cell lymphoma cell lines

机译:CXCR4拮抗剂plerixafor增强利妥昔单抗在弥漫性大B细胞淋巴瘤细胞系中的作用

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摘要

BackgroundDiffuse large B-cell lymphoma (DLBCL) is an aggressive disease with variable clinical outcome, accounting for at least 25-30 % of adult non-Hodgkin lymphomas. Approximately one third of DLBCL patients are not cured by the currently used treatment regimen, R-CHOP. Hence, new treatment strategies are needed. Antagonizing the CXCR4 receptor might be promising since the CXCR4-CXCL12 axis is implicated in several aspects of tumor pathogenesis as well as in protection from chemotherapeutic response. In Burkitt lymphoma, the CXCR4 antagonist plerixafor has already been shown to enhance the therapeutic effect of rituximab, the immunotherapeutic agent of R-CHOP; but this is yet to be confirmed for DLBCL. We, therefore, investigated the effect of plerixafor on DLBCL cellular response to rituximab.
机译:背景弥漫性大B细胞淋巴瘤(DLBCL)是一种侵袭性疾病,临床结果可变,至少占成人非霍奇金淋巴瘤的25-30%。当前使用的治疗方案R-CHOP无法治愈约三分之一的DLBCL患者。因此,需要新的治疗策略。与CXCR4受体拮抗可能是有希望的,因为CXCR4-CXCL12轴涉及肿瘤发病机理的几个方面以及对化学疗法的反应的保护。在伯基特淋巴瘤中,已经证明CXCR4拮抗剂plerixafor可以增强R-CHOP的免疫治疗药物利妥昔单抗的治疗效果。但这对于DLBCL尚待确认。因此,我们研究了plerixafor对DLBCL细胞对利妥昔单抗的反应的作用。

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