Diabetes Division, University of Massachusetts Medical School, Worcester, Massachusetts, USA.
Curr Opin Endocrinol Diabetes Obes. 2010 Apr;17(2):120-5. doi: 10.1097/MED.0b013e328337282f.
Update on humanized mouse models and their use in biomedical research.
The recent description of immunodeficient mice bearing a mutated IL-2 receptor gamma chain (IL2rgamma) facilitated greatly the engraftment and function of human hematolymphoid cells and other cells and tissues. These mice permit the development of human immune systems, including functional T and B cells, following engraftment of hematopoietic stem cells (HSCs). The engrafted functional human immune systems are capable of T and B cell-dependent immune responses, antibody production, antiviral responses, and allograft rejection. Immunodeficient IL2rgamma(null) mice also support heightened engraftment of primary human cancers and malignant progenitor cells, permitting in-vivo investigation of pathogenesis and function. In addition, human-specific infectious agents for which animal models were previously unavailable can now be studied in vivo using these new-generation humanized mice.
Immunodeficient mice bearing an IL2rgamma(null) mutated gene can be engrafted with functional human cells and tissues, including human immune systems, following engraftment with human hematolymphoid cells. These mice are now used as in-vivo models to study human hematopoiesis, immunity, regeneration, stem cell function, cancer, and human-specific infectious agents without putting patients at risk.
更新人源化小鼠模型及其在生物医学研究中的应用。
最近描述的携带突变白细胞介素 2 受体 γ 链(IL-2rgamma)的免疫缺陷小鼠极大地促进了人造血细胞和其他细胞和组织的植入和功能。这些小鼠允许在植入造血干细胞(HSCs)后发展人类免疫系统,包括功能性 T 和 B 细胞。植入的功能性人类免疫系统能够进行 T 和 B 细胞依赖性免疫反应、抗体产生、抗病毒反应和同种异体移植物排斥反应。免疫缺陷的 IL2rgamma(null) 小鼠还支持原发性人类癌症和恶性祖细胞的高植入,允许在体内研究发病机制和功能。此外,现在可以使用这些新一代人源化小鼠在体内研究以前没有动物模型的人类特异性传染性病原体。
携带 IL-2rgamma(null)突变基因的免疫缺陷小鼠可以在植入人造血细胞和组织后,包括人类免疫系统,进行功能性人细胞和组织的植入。这些小鼠现在被用作体内模型,用于研究人类造血、免疫、再生、干细胞功能、癌症和人类特异性传染性病原体,而不会使患者面临风险。