Taya M, Haimovich J
Department of Human Microbiology, Sackler School of Medicine, Tel-Aviv University, Israel.
Cancer Immunol Immunother. 1991;34(1):43-8. doi: 10.1007/BF01741323.
Immunotherapy of a murine B-cell lymphoma by antibodies to idiotypic determinants of its IgM, resulted in surviving tumour-free mice. Several of these mice, however, did develop tumours a long time after the initial inoculation of the tumour cells, or upon rechallenge of the survivors with B-lymphoma cells. The presence of tumour cells during this long latent period may have been due to the development in the host of an anti-idiotype immune response. These late-developing tumours were detected by a radioimmunoassay and characterized by immunofluorescent staining and sodium dodecyl sulphate/polyacrylamide gel electrophoresis. Cells of some late-developing tumours lost the idiotype recognized by the antibodies used for the immunotherapy. Several of these tumours expressed IgM on the cell surface, while others did not, because of the absence of light chains. They were identical in the structure of their rearranged mu chain genes proving their derivation from the original inoculation. Cell lines obtained from the late-developing tumours differed in their tumorigenicity. The appearance of idiotype-negative tumour cells as a result of anti-idiotype immunotherapy has a great impact in our efforts to cure lymphoma by this modality.
用针对小鼠B细胞淋巴瘤IgM独特型决定簇的抗体进行免疫治疗,可使小鼠存活且无肿瘤。然而,其中几只小鼠在最初接种肿瘤细胞很长时间后,或在用B淋巴瘤细胞再次攻击存活小鼠时,确实发生了肿瘤。在这个漫长的潜伏期内肿瘤细胞的存在可能是由于宿主中抗独特型免疫反应的发展。这些后期发生的肿瘤通过放射免疫测定法检测,并通过免疫荧光染色和十二烷基硫酸钠/聚丙烯酰胺凝胶电泳进行表征。一些后期发生的肿瘤细胞失去了用于免疫治疗的抗体所识别的独特型。这些肿瘤中有几个在细胞表面表达IgM,而其他的则由于缺乏轻链而不表达。它们重排的μ链基因结构相同,证明它们源自最初的接种。从后期发生的肿瘤中获得的细胞系在致瘤性方面有所不同。抗独特型免疫治疗导致独特型阴性肿瘤细胞的出现,对我们用这种方式治愈淋巴瘤的努力有很大影响。