Arnold B, Burgert H G, Hamann U, Hämmerling G, Kees U, Kvist S
Cell. 1984 Aug;38(1):79-87. doi: 10.1016/0092-8674(84)90528-2.
We have genetically engineered three alleles of the K locus of the major histocompatibility complex (MHC) of the mouse. These novel hybrid H-2K genes were introduced into mouse 1T 22-6 cells (H-2q), and their products were shown to be expressed on the cell surface. The hybrid H-2 K antigens were examined for their ability to function as restricting elements for cytotoxic T lymphocytes during influenza A infection. Both the alpha 1 and alpha 2 domains of the Kd antigen were required for T cell recognition. This implies an important role for "conformational determinants" on H-2 antigens acting as restricting elements. The cytoplasmic domain of the Kb antigen is not phenotypically important for recognition by T cells.
我们通过基因工程构建了小鼠主要组织相容性复合体(MHC)K位点的三个等位基因。这些新型杂交H-2K基因被导入小鼠1T 22-6细胞(H-2q),其产物在细胞表面表达。检测了杂交H-2 K抗原在甲型流感病毒感染期间作为细胞毒性T淋巴细胞限制元件发挥作用的能力。T细胞识别需要Kd抗原的α1和α2结构域。这意味着H-2抗原上的“构象决定簇”作为限制元件起着重要作用。Kb抗原的胞质结构域在T细胞识别方面在表型上并不重要。