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在人源化小鼠中模拟人类白血病免疫疗法

Modeling Human Leukemia Immunotherapy in Humanized Mice.

作者信息

Xia Jinxing, Hu Zheng, Yoshihara Satoshi, Li Yuying, Jin Chun-Hui, Tan Shulian, Li Wei, Chen Qingfeng, Sykes Megan, Yang Yong-Guang

机构信息

Columbia Center for Translational Immunology, Department of Medicine, Columbia University College of Physicians and Surgeons, New York, USA; Department of Clinical Laboratory, The First Affiliated Hospital of Anhui Medical University, Hefei, China.

Columbia Center for Translational Immunology, Department of Medicine, Columbia University College of Physicians and Surgeons, New York, USA; The First Hospital and Institute of Immunology, Jilin University, Changchun, China.

出版信息

EBioMedicine. 2016 Aug;10:101-8. doi: 10.1016/j.ebiom.2016.06.028. Epub 2016 Jun 23.

Abstract

The currently available human tumor xenograft models permit modeling of human cancers in vivo, but in immunocompromised hosts. Here we report a humanized mouse (hu-mouse) model made by transplantation of human fetal thymic tissue plus hematopoietic stem cells transduced with a leukemia-associated fusion gene MLL-AF9. In addition to normal human lymphohematopoietic reconstitution as seen in non-leukemic hu-mice, these hu-mice showed spontaneous development of B-cell acute lymphoblastic leukemia (B-ALL), which was transplantable to secondary recipients with an autologous human immune system. Using this model, we show that lymphopenia markedly improves the antitumor efficacy of recipient leukocyte infusion (RLI), a GVHD-free immunotherapy that induces antitumor responses in association with rejection of donor chimerism in mixed allogeneic chimeras. Our data demonstrate the potential of this leukemic hu-mouse model in modeling leukemia immunotherapy, and suggest that RLI may offer a safe treatment option for leukemia patients with severe lymphopenia.

摘要

目前可用的人肿瘤异种移植模型允许在免疫功能低下的宿主中在体内对人类癌症进行建模。在此,我们报告一种人源化小鼠(hu-小鼠)模型,该模型通过移植人胎儿胸腺组织以及用白血病相关融合基因MLL-AF9转导的造血干细胞制成。除了在非白血病hu-小鼠中所见的正常人类淋巴细胞造血重建外,这些hu-小鼠还表现出B细胞急性淋巴细胞白血病(B-ALL)的自发发展,并且可移植到具有自体人类免疫系统的二级受体中。使用该模型,我们表明淋巴细胞减少显著提高了受体白细胞输注(RLI)的抗肿瘤功效,RLI是一种无移植物抗宿主病(GVHD)的免疫疗法,可在混合异基因嵌合体中诱导抗肿瘤反应并伴有供体嵌合体的排斥。我们的数据证明了这种白血病hu-小鼠模型在白血病免疫治疗建模中的潜力,并表明RLI可能为严重淋巴细胞减少的白血病患者提供一种安全的治疗选择。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ec9f/5006579/c18f71d41c9d/gr1.jpg

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