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建立人源化小鼠模型,使用外周血单个核细胞或脐带血 CD34+造血干细胞,用于免疫肿瘤学研究评估新型治疗药物。

Establishment of Humanized Mice from Peripheral Blood Mononuclear Cells or Cord Blood CD34+ Hematopoietic Stem Cells for Immune-Oncology Studies Evaluating New Therapeutic Agents.

机构信息

Champions Oncology, Rockville, Maryland.

出版信息

Curr Protoc Pharmacol. 2020 Jun;89(1):e77. doi: 10.1002/cpph.77.

Abstract

The clinical success of immune checkpoint modulators and the development of next-generation immune-oncology (IO) agents underscore the need for robust preclinical models to evaluate novel IO therapeutics. Human immune system (HIS) mouse models enable in vivo studies in the context of the HIS via a human tumor. The immunodeficient mouse strains NOG (Prkdc Il2rg ) and triple-transgenic NOG-EXL [Prkdc Il2rg Tg (SV40/HTLV-IL3, CSF2)], which expresses human IL-3 and GM-CSF, allow for human CD34+ hematopoietic stem cell (huCD34+ HSC) engraftment and multilineage immune cell development by 12 to 16 weeks post-transplant and facilitate studies of immunomodulatory agents. A more rapid model of human immune engraftment utilizes peripheral blood mononuclear cells (PBMCs) transplanted into immunodeficient murine hosts, permitting T-cell engraftment within 2 to 3 weeks without outgrowth of other human immune cells. The PBMC-HIS model can be limited due to onset of xenogeneic graft-versus-host disease (xGVHD) within 3 to 5 weeks post-implantation. Host deficiency in MHC class I, as occurs in beta-2 microglobulin knockout in either NOG or NSG mice, results in resistance to xGVHD, which permits a longer therapeutic window. In this article, detailed processes for generating humanized mice by transplantation of HSCs from cord blood-derived huCD34+ HSCs or PBMCs into immunodeficient mouse strains to respectively generate HSC-HIS and PBMC-HIS mouse models are provided. In addition, the co-engraftment and growth kinetics of patient-derived and cell line-derived xenograft tumors in humanized mice and recovery of tumor-infiltrating lymphocytes from growing tumors to evaluate immune cell subsets by flow cytometry are described. © 2020 The Authors. Basic Protocol 1: Establishment of patient-derived xenograft tumors in CD34+ hematopoietic stem cell-humanized mice Basic Protocol 2: Establishment of patient-derived xenograft tumors in peripheral blood mononuclear cell-humanized mice Support Protocol 1: Flow cytometry assessment of humanization in mice Support Protocol 2: Flow cytometry assessment of tumor-infiltrating lymphocytes in tumor-bearing humanized mouse models.

摘要

免疫检查点调节剂的临床成功和下一代免疫肿瘤学(IO)药物的发展突显了需要强大的临床前模型来评估新型 IO 治疗药物。人类免疫系统(HIS)小鼠模型通过人类肿瘤在 HIS 背景下进行体内研究。免疫缺陷小鼠品系 NOG(Prkdc Il2rg)和三重转基因 NOG-EXL[Prkdc Il2rg Tg(SV40/HTLV-IL3,CSF2)],表达人 IL-3 和 GM-CSF,允许人 CD34+造血干细胞(huCD34+HSC)在移植后 12 至 16 周内植入和多种免疫细胞的发育,并促进免疫调节剂的研究。一种更快速的人类免疫植入模型利用外周血单核细胞(PBMC)移植到免疫缺陷的鼠宿主中,在 2 至 3 周内允许 T 细胞植入,而不会有其他人类免疫细胞的过度生长。PBMC-HIS 模型可能会受到限制,因为在植入后 3 至 5 周内会发生异种移植物抗宿主病(xGVHD)。在 NOG 或 NSG 小鼠中存在 MHC 类 I 基因缺失的宿主缺陷会导致对 xGVHD 的抗性,从而延长治疗窗口。在本文中,提供了详细的过程,用于通过将脐带血来源的 huCD34+HSC 或 PBMC 移植到免疫缺陷小鼠品系中来生成人源化小鼠,以分别生成 HSC-HIS 和 PBMC-HIS 小鼠模型。此外,描述了患者来源和细胞系来源的异种移植物肿瘤在人源化小鼠中的共同植入和生长动力学以及从生长肿瘤中回收肿瘤浸润淋巴细胞以通过流式细胞术评估免疫细胞亚群。

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