van der Poel J J, Pool J, Goulmy E, Giphart M J, van Rood J J
Hum Immunol. 1986 Jul;16(3):247-58. doi: 10.1016/0198-8859(86)90052-2.
Alloimmune CTLs specifically recognizing the HLA-A2.3 subtype could be made besides the previously described HLA-A2.1 and A2.2 subtype-specific CTLs. Examination of the fine specificity of 15 different CTLs directed against distinct HLA-A2 subtypes demonstrated further complexity of antigenic epitopes present on the A2 molecule. First, epitopes could be defined which are unique for the HLA-A2.1, A2.2, A2.3, and A2.4 subtypes. Second, epitopes could be defined which are shared between the HLA-A2.1, A2.2 and A2.4 subtypes, but which are not shared by the A2.3 subtype. Analysis of the reactivity patterns of CTLs directed against the HLA-A2.2 and A2.4 subtypes indicated that the observed cytotoxic response was dependent on the HLA type of the responder cell. Biochemical analysis demonstrated the existence of isoelectric point variation in A2 heavy chains which deviated from the expected pIs for the A2 subtypes as described previously. Individuals were identified who possessed A2 heavy chains typical for the A2.3 subtype antigen although the CTL analysis demonstrated the presence of an A2.1 subtype antigen.
除了先前描述的针对HLA - A2.1和A2.2亚型的特异性CTL外,还可以制备特异性识别HLA - A2.3亚型的同种异体免疫CTL。对15种针对不同HLA - A2亚型的不同CTL的精细特异性进行检测,结果表明A2分子上存在的抗原表位具有进一步的复杂性。首先,可以确定对HLA - A2.1、A2.2、A2.3和A2.4亚型具有独特性的表位。其次,可以确定在HLA - A2.1、A2.2和A2.4亚型之间共享,但A2.3亚型不共享的表位。对针对HLA - A2.2和A2.4亚型的CTL反应模式的分析表明,观察到的细胞毒性反应取决于反应细胞的HLA类型。生化分析表明,A2重链存在等电点变化,与先前描述的A2亚型预期的pI不同。已鉴定出一些个体,尽管CTL分析显示存在A2.1亚型抗原,但他们拥有A2.3亚型抗原典型的A2重链。