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Use of CXCR4-antagonist for haematopoietic stem cell mobilization in HIV-infected patients with haematological malignancies

机译:CXCR4拮抗剂在HIV感染的血液系统恶性肿瘤患者中用于造血干细胞动员的应用

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摘要

The introduction of highly active antiretroviral therapy has profoundly modified the management of HIV-associated haematologic malignancies, making aggressive therapy, including autologous or allogeneic stem cell transplantation, a fascinating tool for treating patients [1]. However, HIV infection has been described as a risk factor for poor mobilization [2]. Plerixafor acts by selective and reversible antagonism of CXCR4 on CD34~+ haematopoietic stem cells. This results in disruption of its interaction with CXCL12 (formally SDF1) on bone marrow (BM) stromal cells, that causes a rapid release of stem and progenitor cells from BM into peripheral blood, facilitating their collection through apheresis methods [3,4].
机译:高活性抗逆转录病毒疗法的引入极大地改变了与HIV相关的血液系统恶性肿瘤的治疗方法,使包括自体或异体干细胞移植在内的积极疗法成为治疗患者的诱人工具[1]。然而,艾滋病毒感染已被描述为动员不力的危险因素[2]。 Plerixafor通过CXCR4对CD34〜+造血干细胞的选择性和可逆拮抗作用。这导致其与骨髓(BM)基质细胞上的CXCL12(前身为SDF1)的相互作用破坏,从而导致干细胞和祖细胞从BM快速释放到外周血中,从而通过采血方法促进了它们的收集[3,4]。

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