Grusby M J, Glimcher L H
Department of Cancer Biology, Harvard School of Public Health, Boston, Massachusetts 02115, USA.
Annu Rev Immunol. 1995;13:417-35. doi: 10.1146/annurev.iy.13.040195.002221.
Major histocompatibility complex (MHC) class II molecules are heterodimeric cell surface proteins that are critically important for the development and function of cells in the immune system. In particular, the maturation of CD4+ T cells is dependent on the expression of MHC class II molecules on thymic epithelium, while the activation of these cells requires the expression of class II molecules on specialized antigen-presenting cells in the periphery. The importance of class II molecules is especially evident in humans who are afflicted with MHC class II-deficient combined immunodeficiency, as these individuals die at an early age unless provided with a bone marrow transplant. Here we discuss the functional consequences of MHC class II deficiency in a mouse model generated by gene targeting in embryonic stem (ES) cells. These mice have proved to be valuable reagents for dissecting the mechanisms by which MHC class II molecules control the maturation and activation of lymphocytes as well as for elucidating the role of these cells in various immune responses.
主要组织相容性复合体(MHC)II类分子是异二聚体细胞表面蛋白,对免疫系统中细胞的发育和功能至关重要。特别是,CD4 + T细胞的成熟依赖于胸腺上皮细胞上MHC II类分子的表达,而这些细胞的激活则需要外周专门的抗原呈递细胞上II类分子的表达。II类分子的重要性在患有MHC II类缺陷联合免疫缺陷的人类中尤为明显,因为这些个体除非接受骨髓移植,否则会在早年死亡。在这里,我们讨论了通过胚胎干细胞(ES)细胞基因靶向产生的小鼠模型中MHC II类缺陷的功能后果。这些小鼠已被证明是剖析MHC II类分子控制淋巴细胞成熟和激活机制以及阐明这些细胞在各种免疫反应中作用的有价值试剂。