Andrew M. and Jane M. Bursky Center for Human Immunology and Immunotherapy Programs, Washington University School of Medicine, Saint Louis, MO, USA.
Division of Infectious Diseases, Department of Medicine, Washington University School of Medicine, Saint Louis, MO, USA.
Methods Mol Biol. 2022;2463:53-66. doi: 10.1007/978-1-0716-2160-8_5.
Humanized mice, which we define as immunodeficient mice that have been reconstituted with a human immune system, represent promising preclinical models for translational research and precision medicine as they allow modeling and therapy of human diseases in vivo. The first generation of humanized mice showed insufficient development, diversity and function of human immune cells, in particular human natural killer (NK) cells and type 1 innate lymphoid cells (ILC1). This limited the applicability of humanized mice for studying ILC1 and NK cells in the context of human cancers and immunotherapeutic manipulation. However, since 2014, several next-generation humanized mouse models have been developed that express human IL-15 either as a transgene or knock-in (NOG-IL15, NSG-IL15, NSG-IL7-IL15, SRG-15) or show improved development of human myeloid cells, which express human IL-15 and thereby promote human NK cell development (NSG-SGM3, MISTRG, BRGSF). Here we compare the various next-generation humanized mouse models and describe the methodological procedures for creating mice with a functioning human immune system and how they can be used to study and manipulate human NK cells in health and disease.
人源化小鼠,我们将其定义为经过重建以具有人类免疫系统的免疫缺陷小鼠,代表了有前途的临床前模型,可用于转化研究和精准医学,因为它们允许在体内模拟和治疗人类疾病。第一代人源化小鼠显示出人类免疫细胞,特别是人类自然杀伤 (NK) 细胞和 1 型先天淋巴细胞 (ILC1) 的发育、多样性和功能不足。这限制了人源化小鼠在研究人类癌症和免疫治疗操作背景下的 ILC1 和 NK 细胞的适用性。然而,自 2014 年以来,已经开发了几种下一代人源化小鼠模型,这些模型要么作为转基因表达人白细胞介素 15 (NOG-IL15、NSG-IL15、NSG-IL7-IL15、SRG-15),要么显示出人类髓样细胞的发育得到改善,这些细胞表达人白细胞介素 15,从而促进人类 NK 细胞的发育 (NSG-SGM3、MISTRG、BRGSF)。在这里,我们比较了各种下一代人源化小鼠模型,并描述了创建具有功能人类免疫系统的小鼠的方法学程序,以及如何将其用于研究和操纵健康和疾病中的人类 NK 细胞。