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增强人骨髓纤维化干/祖细胞在 MISTRG 小鼠中的植入。

Enhanced engraftment of human myelofibrosis stem and progenitor cells in MISTRG mice.

机构信息

Department of Medical Oncology and Hematology, University of Zurich and University Hospital Zurich, Zurich, Switzerland.

Institute of Pathology and Molecular Pathology, University Hospital Zurich, Zurich, Switzerland.

出版信息

Blood Adv. 2020 Jun 9;4(11):2477-2488. doi: 10.1182/bloodadvances.2019001364.

Abstract

The engraftment potential of myeloproliferative neoplasms in immunodeficient mice is low. We hypothesized that the physiological expression of human cytokines (macrophage colony-stimulating factor, interleukin-3, granulocyte-macrophage colony-stimulating factor, and thrombopoietin) combined with human signal regulatory protein α expression in Rag2-/-Il2rγ-/- (MISTRG) mice might provide a supportive microenvironment for the development and maintenance of hematopoietic stem and progenitor cells (HSPC) from patients with primary, post-polycythemia or post-essential thrombocythemia myelofibrosis (MF). We show that MISTRG mice, in contrast to standard immunodeficient NOD.Cg-PrkdcscidIl2rgtm1Wjl/SzJ and Rag2-/-Il2rγ-/- mice, supported engraftment of all patient samples investigated independent of MF disease stage or risk category. Moreover, MISTRG mice exhibited significantly higher human MF engraftment levels in the bone marrow, peripheral blood, and spleen and supported secondary repopulation. Bone marrow fibrosis development was limited to 3 of 14 patient samples investigated in MISTRG mice. Disease-driving mutations were identified in all xenografts, and targeted sequencing revealed maintenance of the primary patient sample clonal composition in 7 of 8 cases. Treatment of engrafted mice with the current standard-of-care Janus kinase inhibitor ruxolitinib led to a reduction in human chimerism. In conclusion, the established MF patient-derived xenograft model supports robust engraftment of MF HSPCs and maintains the genetic complexity observed in patients. The model is suited for further testing of novel therapeutic agents to expedite their transition into clinical trials.

摘要

髓系增殖性肿瘤在免疫缺陷小鼠中的植入潜力较低。我们假设,人细胞因子(巨噬细胞集落刺激因子、白细胞介素-3、粒细胞-巨噬细胞集落刺激因子和血小板生成素)的生理表达与人信号调节蛋白α在 Rag2-/-Il2rγ-/-(MISTRG)小鼠中的表达相结合,可能为原发性、真性红细胞增多症后或特发性血小板增多症后骨髓纤维化(MF)患者的造血干细胞和祖细胞(HSPC)的发育和维持提供支持性微环境。我们表明,与标准免疫缺陷 NOD.Cg-PrkdcscidIl2rgtm1Wjl/SzJ 和 Rag2-/-Il2rγ-/-小鼠相比,MISTRG 小鼠支持所有研究患者样本的植入,而与 MF 疾病阶段或风险类别无关。此外,MISTRG 小鼠在骨髓、外周血和脾脏中表现出明显更高的人 MF 植入水平,并支持二次再植入。在 MISTRG 小鼠中,仅 3 个研究的患者样本中观察到骨髓纤维化的发展。在所有异种移植物中均鉴定出疾病驱动突变,靶向测序显示在 8 例中有 7 例维持了原发性患者样本的克隆组成。用当前标准治疗 Janus 激酶抑制剂芦可替尼治疗植入的小鼠导致人嵌合体减少。总之,已建立的 MF 患者来源异种移植模型支持 MF HSPC 的强大植入,并维持了在患者中观察到的遗传复杂性。该模型适合进一步测试新型治疗剂,以加速它们进入临床试验。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3af1/7284099/22e700f29d09/advancesADV2019001364absf1.jpg

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