Wiels J, Balaña A, Tursz T
IARC Sci Publ. 1985(60):457-64.
We have previously described a monoclonal antibody, referred to as 38.13, reacting with most Burkitt's lymphoma (BL) derived lines, both with and without Epstein-Barr virus (EBV), but not reacting with EBV-positive lymphoblastoid cell lines (Wiels et al., 1981, 1982). The antibody reacted with 41 BL lines out of 57 tested. The target antigen, BLA, was shown to be a neutral glycolipid, identified as globotriaosylceramide (Gal alpha 1----4Gal beta 1----4 Glc beta 1----1 ceramide) (Nudelman et al., 1983). This substance is known as the blood group antigen Pk, a normal intermediate in the P-substance synthesis. The 38.13 antibody was covalently linked to either ricin-A chain or gelonin toxin, and its anti-BL specificity remained unaffected. Both immunotoxins were highly cytotoxic for cultured BL cells. The kinetics of the toxic effects of the immunotoxins on these cells appeared to be strikingly fast, since 50% protein synthesis inhibition was achieved after two hours' incubation. These kinetics are similar to those obtained with entire ricin, and clearly different from those observed when using immunotoxins directed against protein antigens (16-30 h). When longer incubation times are used, killing of apparently irrelevant targets was reproducibly observed. These data suggest the presence of a low number of antigenic sites on non-Burkitt cells. The detection of a low number of antigenic sites by immunotoxins directed towards such glycolipid antigens might not be a disadvantage, but might rather permit efficient and rapid killing of a wide variety of tumour cells.
我们之前描述过一种单克隆抗体,称为38.13,它能与大多数源自伯基特淋巴瘤(BL)的细胞系发生反应,无论这些细胞系是否携带爱泼斯坦-巴尔病毒(EBV),但不与EBV阳性的淋巴母细胞系发生反应(维尔斯等人,1981年、1982年)。在57个测试的BL细胞系中,该抗体与41个细胞系发生了反应。靶抗原BLA被证明是一种中性糖脂,鉴定为球三糖神经酰胺(半乳糖α1→4半乳糖β1→4葡萄糖β1→1神经酰胺)(努德尔曼等人,1983年)。这种物质就是血型抗原Pk,是P物质合成过程中的一种正常中间体。38.13抗体与蓖麻毒素A链或去甲氧基蓖麻毒素共价连接,其抗BL特异性不受影响。两种免疫毒素对培养的BL细胞都具有高度细胞毒性。免疫毒素对这些细胞的毒性作用动力学似乎非常快,因为孵育两小时后就能实现50%的蛋白质合成抑制。这些动力学与使用完整蓖麻毒素时得到的结果相似,与针对蛋白质抗原的免疫毒素观察到的结果(16 - 30小时)明显不同。当使用更长的孵育时间时,可重复性地观察到对明显无关靶标的杀伤作用。这些数据表明非伯基特细胞上存在少量抗原位点。针对此类糖脂抗原的免疫毒素检测到少量抗原位点可能并非劣势,反而可能允许高效快速地杀伤多种肿瘤细胞。