Vaccine and Gene Therapy Institute, Oregon Health and Science University, Portland, OR, USA.
Methods Mol Biol. 2021;2244:343-363. doi: 10.1007/978-1-0716-1111-1_17.
Immunodeficient mice engrafted with human tissues provide a robust model for the in vivo investigation of human-restricted viruses such as human cytomegalovirus (HCMV). Several humanized mouse models have been developed and improved over the last 30 years. Here, we describe a protocol for the transplant of human hematopoietic stem cells with autologous fetal liver and thymic tissues into NOD.Cg-PrkdcIL2rγ mice to create a humanized bone marrow-liver-thymus model (huBLT) that can be infected with HCMV. The presence of human thymus allows the development of a functional human immune system, including HLA-restricted human T-cells and B-cells. Indeed, following infection, huBLT mice generate virus-specific CD4+ and CD8+ T-cell responses. Additionally, both HCMV-specific IgM and IgG B-cell responses can be detected. This huBLT model provides the first animal model to explore the adaptive human immune response to HCMV infection.
免疫缺陷小鼠移植人组织可提供用于研究人类受限病毒(如人类巨细胞病毒,HCMV)的体内模型。在过去的 30 多年中,已经开发并改进了几种人源化小鼠模型。在这里,我们描述了一种将人造血干细胞与自体胎肝和胸腺组织移植到 NOD.Cg-PrkdcIL2rγ小鼠中以创建可感染 HCMV 的人骨髓-肝脏-胸腺模型(huBLT)的方案。人胸腺的存在可使人免疫系统发挥功能,包括 HLA 受限的人类 T 细胞和 B 细胞。实际上,在感染后,huBLT 小鼠会产生针对病毒的 CD4+和 CD8+T 细胞应答。此外,还可以检测到 HCMV 特异性 IgM 和 IgG B 细胞应答。该 huBLT 模型提供了首个探索适应性人类对 HCMV 感染的免疫反应的动物模型。