Forman J, Vitetta E S, Hart D A
J Immunol. 1977 Mar;118(3):803-8.
Spleen cells were modified with varying concentrations of trinitrobenzene sulfonic acid and then assayed for both their ability to stimulate syngeneic spleen cells into displaying a cytotoxic effect against TNP-modified target cells and for the extent of TNP derivatization of H-2 antigens. It was found that there was a direct correlation between the extent of derivatization of H-2 antigens and the ability of such derivatized cells to act as stimulator cells in the TNP-CML assay. Thus, these data lend support to the altered self or interaction antigen hypothesis as the explanation for the H-2 gene restriction of syngeneic CML. Target cells were also modified with TNBS at varying concentrations to determine the optimal concentration required to permit lysis in the CML assay. The results of these experiments indicate that similar concentration ranges of TNBS are required to create antigenic determinants on the target cells as well as immunogenic determinants on the stimulator cells that can be recognized by cytotoxic T cells.
用不同浓度的三硝基苯磺酸修饰脾细胞,然后检测其刺激同基因脾细胞对三硝基苯(TNP)修饰的靶细胞产生细胞毒性作用的能力,以及H-2抗原的TNP衍生化程度。结果发现,H-2抗原的衍生化程度与这种衍生化细胞在TNP-慢性粒细胞白血病(CML)检测中作为刺激细胞的能力之间存在直接相关性。因此,这些数据支持了改变的自身或相互作用抗原假说,以此来解释同基因CML的H-2基因限制。还用不同浓度的TNBS修饰靶细胞,以确定在CML检测中允许细胞裂解所需的最佳浓度。这些实验结果表明,在靶细胞上产生抗原决定簇以及在刺激细胞上产生可被细胞毒性T细胞识别的免疫原性决定簇,需要相似浓度范围的TNBS。