Hulette C M, Effros R B, Dillard L C, Walford R L
Am J Pathol. 1985 Oct;121(1):10-4.
An Epstein-Barr-virus-transformed lymphoblastoid cell line (ECEBV) was derived from a multiply transfused renal dialysis patient. ECEBV was shown to secrete specific antibody in a cellular enzyme-linked immunosorbent assay (CELISA) and was hybridized with the mutagenized human fusion partner G M1500 resistant to 6-thioguanine and ouabain. Hybridomas surviving hypoxanthine-aminopterin-thymidine (HAT) and ouabain selection were cloned by limiting dilution. The hybridomas continue to secrete antibody which reacts with some human cells but not with others after 14 months in culture. None reacts with K562 (no HLA-A, -B, -C or -DR) or with Daudi (no HLA-A, -B, or -C). This is a preliminary report of the production of a human monoclonal antibody to HLA. Application of this technique could result in the large-scale production of human monoclonal antibodies for HLA typing, the production of anti-idiotype antibodies for use in transplant patients to prevent acute rejection, and for the study of the structure and function of HLA in man.
一株爱泼斯坦-巴尔病毒转化的淋巴母细胞系(ECEBV)源自一名多次输血的肾透析患者。在细胞酶联免疫吸附测定(CELISA)中,ECEBV被证明能分泌特异性抗体,并与对6-硫鸟嘌呤和哇巴因耐药的诱变人融合伙伴GM1500杂交。通过有限稀释法对在次黄嘌呤-氨基蝶呤-胸腺嘧啶核苷(HAT)和哇巴因选择中存活的杂交瘤进行克隆。这些杂交瘤在培养14个月后仍继续分泌与一些人类细胞反应但不与其他细胞反应的抗体。没有一个与K562(无HLA-A、-B、-C或-DR)或Daudi(无HLA-A、-B或-C)反应。这是关于一种抗HLA人单克隆抗体产生的初步报告。应用该技术可大规模生产用于HLA分型的人单克隆抗体、用于移植患者预防急性排斥的抗独特型抗体,以及用于研究人类HLA的结构和功能。