Cantor H, Boyse E A
J Exp Med. 1975 Jun 1;141(6):1390-9. doi: 10.1084/jem.141.6.1390.
Lymphocytes from BALB/c or C57B6/6 mice that develop killer activity to alloantigens belong to the numerically small Ly-23 subclass of peripheral T cells, distinguished by selective expression of Ly-23 determinants on their surfaces. The maturation of these cells to killer cells can be amplified by Ly-1+ cells, which do not themselves contribute to the killer cell pool. This amplification was abolished by escluding Ia("Beta")+ cells from the stimulator population during mixed lymphocyte culture (MCL), suggesting that amplification is due to selective recognition of I region antigens by L-1+ cells, a conclusion already drawn from our previous evidence that Ia differences activate Ly-1+ cells but not Ly-23+ cells. These and other experiments indicate that amplification of killer cell production in vitro by Ly-1+ cells is not due to their conversion to Ly-23+ cells during MLC, but to their ability to recognize major histocompatibility complex determinants not recognized by Ly-23+ cells.
对同种抗原产生杀伤活性的BALB/c或C57B6/6小鼠的淋巴细胞属于外周T细胞中数量较少的Ly-23亚类,其特征是在细胞表面选择性表达Ly-23决定簇。这些细胞向杀伤细胞的成熟过程可被Ly-1+细胞增强,而Ly-1+细胞本身并不参与杀伤细胞库的形成。在混合淋巴细胞培养(MCL)过程中,通过从刺激细胞群体中排除Ia(“β”)+细胞,这种增强作用被消除,这表明增强作用是由于Ly-1+细胞对I区抗原的选择性识别,这一结论已从我们之前的证据中得出,即Ia差异激活Ly-1+细胞而非Ly-23+细胞。这些以及其他实验表明,Ly-1+细胞在体外对杀伤细胞产生的增强作用并非由于它们在MLC过程中转化为Ly-23+细胞,而是由于它们识别Ly-23+细胞无法识别的主要组织相容性复合体决定簇的能力。