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氟达拉滨作为一种具有成本效益的辅助药物,可增强免疫缺陷小鼠中人类正常和恶性造血的植入。

Fludarabine as a cost-effective adjuvant to enhance engraftment of human normal and malignant hematopoiesis in immunodeficient mice.

机构信息

M. Tettamanti Research Center, Department of Pediatrics, University of Milano-Bicocca, Monza, 20900, Italy.

Department of Haemato-Oncology, Rayne Institute, King's College London, London, SE59NU, UK.

出版信息

Sci Rep. 2018 Jun 14;8(1):9125. doi: 10.1038/s41598-018-27425-x.

Abstract

There is still an unmet need for xenotransplantation models that efficiently recapitulate normal and malignant human hematopoiesis. Indeed, there are a number of strategies to generate humanized mice and specific protocols, including techniques to optimize the cytokine environment of recipient mice and drug alternatives or complementary to the standard conditioning regimens, that can be significantly modulated. Unfortunately, the high costs related to the use of sophisticated mouse models may limit the application of these models to studies that require an extensive experimental design. Here, using an affordable and convenient method, we demonstrate that the administration of fludarabine (Fludara) promotes the extensive and rapid engraftment of human normal hematopoiesis in immunodeficient mice. Quantification of human CD45 cells in bone marrow revealed approximately a 10-fold increase in mice conditioned with irradiation plus fludarabine. Engrafted cells in the bone marrow included hematopoietic stem cells, as well as myeloid and lymphoid cells. Moreover, this model proved to be sufficient for robust reconstitution of malignant myeloid hematopoiesis, permitting primary acute myeloid leukemia cells to engraft as early as 8 weeks after the transplant. Overall, these results present a novel and affordable model for engraftment of human normal and malignant hematopoiesis in immunodeficient mice.

摘要

目前仍然需要能够高效重现正常和恶性人类造血的异种移植模型。事实上,有许多生成人源化小鼠的策略和具体方案,包括优化受体小鼠细胞因子环境的技术,以及可显著调节的标准条件方案的替代药物或补充药物。不幸的是,使用复杂的小鼠模型相关的高成本可能会限制这些模型在需要广泛实验设计的研究中的应用。在这里,我们使用一种经济实惠且方便的方法证明,氟达拉滨(Fludara)的给药可促进免疫缺陷小鼠中人类正常造血的广泛和快速植入。通过对骨髓中人类 CD45 细胞的定量分析,发现辐照加氟达拉滨处理的小鼠中细胞数量增加了约 10 倍。骨髓中植入的细胞包括造血干细胞以及髓系和淋巴系细胞。此外,该模型足以有效地重建恶性髓系造血,允许原发性急性髓系白血病细胞在移植后 8 周内即可植入。总的来说,这些结果为免疫缺陷小鼠中人类正常和恶性造血的植入提供了一种新颖且经济实惠的模型。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0990/6002385/fd6023526780/41598_2018_27425_Fig1_HTML.jpg

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