Hanna R, Ong G L, Mattes M J
Garden State Cancer Center, Center for Molecular Medicine and Immunology, Newark, New Jersey 07103, USA.
Cancer Res. 1996 Jul 1;56(13):3062-8.
In an attempt to recognize general patterns in the processing of Abs (antibodies) bound to the surface of tumor cells, eight monoclonal antibodies were tested on 10 hematological malignancies of various histological types. The results were compared with previous findings obtained with carcinomas, melanomas, and gliomas, using some of the same antibodies. The data demonstrated that some B-cell lymphomas appear to be unusual in that Abs were unable to bind to them irreversibly; except for those Abs that were rapidly internalized, none of the Abs tested was able to bind irreversibly to the B-cell lymphomas Raji or RL. In contrast, most Abs bound irreversibly to the tumors of other histological types, including other hematological tumors. Irreversible Ab binding to B-cell lymphomas was achieved by cross-linking the Abs on the cell surface. Such differences between cell lines may be due to differences in the supramolecular structure of the surface membrane, which affect the frequency or stability of bivalent Ab binding. The Ab binding interaction could not be described in terms of "functional affinity." These results may lead to improvements in the use of Abs for tumor immunotherapy and for other purposes.
为了识别与肿瘤细胞表面结合的抗体(Abs)处理过程中的一般模式,对8种单克隆抗体在10种不同组织学类型的血液系统恶性肿瘤上进行了测试。使用其中一些相同的抗体,将结果与先前在癌、黑色素瘤和胶质瘤上获得的结果进行了比较。数据表明,一些B细胞淋巴瘤似乎不寻常,因为抗体无法不可逆地结合到它们上面;除了那些被快速内化的抗体外,所测试的抗体中没有一种能够不可逆地结合到B细胞淋巴瘤Raji或RL上。相比之下,大多数抗体不可逆地结合到其他组织学类型的肿瘤上,包括其他血液系统肿瘤。通过交联细胞表面的抗体实现了抗体与B细胞淋巴瘤的不可逆结合。细胞系之间的这种差异可能是由于表面膜超分子结构的差异,这影响了二价抗体结合的频率或稳定性。抗体结合相互作用不能用“功能亲和力”来描述。这些结果可能会改进抗体在肿瘤免疫治疗和其他用途中的应用。