Hansen J A, Martin P J, Kamoun M, Nisperos B, Thomas E D
Hum Immunol. 1981 Mar;2(2):103-11. doi: 10.1016/0198-8859(81)90057-4.
The hybridoma technique was used to produce a monoclonal antibody specific for a polymorphic determinant on human la antigens. BALB/c mice were immunized with a B-lymphoblastoid cell line derived from an HLA-DR3/DR4 positive donor. Hybridoma culture supernates were screened in two stages by means of the microcytotoxicity assay. Supernates were first tested against the la-positive immunizing cell line and against la-negative cells. Cultures identified as producing antibody cytoxic for the immunizing cell line but not for la-negative cells were subcultured and the supernates then tested against a selected panel of HLA-D homozygous cell lines (HCL). In this manner, it was possible to identify a microwell of hybrid cells producing an antibody that reacted with a polymorphic HLA-DR determinant. Cells from this culture, designated 17.15, were cloned twice by limiting dilution. Specificity was evaluated with a panel of 39 HCL and B cells from 70 normal donors. Antibody 17.15 recognized a supertypic DR "4 + 5" specificity, which was also present on DRw9 and some DR7 positive cells. These findings suggest that the cross-reactivity groups DR "4 + 5" (MB-3) and DR "4 + 7" (MT-3) defined by alloantisera may share a common supertypic specificity that is recognized by monoclonal antibody 17.15.
采用杂交瘤技术制备针对人白细胞抗原(la)多态性决定簇的单克隆抗体。用源自一名HLA - DR3/DR4阳性供体的B淋巴母细胞系免疫BALB/c小鼠。通过微量细胞毒性试验分两个阶段筛选杂交瘤培养上清液。首先针对la阳性的免疫细胞系和la阴性细胞检测上清液。鉴定为产生针对免疫细胞系具有细胞毒性但对la阴性细胞无细胞毒性抗体的培养物进行传代培养,然后针对一组选定的HLA - D纯合细胞系(HCL)检测上清液。通过这种方式,能够鉴定出产生与多态性HLA - DR决定簇反应的抗体的杂交细胞微孔。来自该培养物的细胞,命名为17.15,通过有限稀释法克隆了两次。用一组39个HCL和来自70名正常供体的B细胞评估特异性。抗体17.15识别一种超型DR“4 + 5”特异性,其也存在于DRw9和一些DR7阳性细胞上。这些发现表明,由同种抗血清定义的交叉反应组DR“4 + 5”(MB - 3)和DR“4 + 7”(MT - 3)可能共享一种被单克隆抗体17.15识别的共同超型特异性。