Srinivasa Rao V, Bonavida B
Cancer Res. 1977 Sep;37(9):3385-9.
Circulating soluble tumor antigens were detected in the serum of tumor-bearing rats. Sublethally irradiated W/Fu rats inoculated with syngeneic C58(NT)D Gross virus-induced lymphoma served as the source of tumor antigens. Soluble antigens were assessed by specific inhibition of the complement-mediated cytotoxicity of isogenic W/Fu anti-C58(NT)D antibodies against 51Cr tumor target cells. With a s.c. inoculum of 5 X 10(7) tumor cells, circulating tumor antigens were first detected at Day 8, and a maximum concentration was reached by Day 13 to 14, which coincided with the peak of tumor growth and was followed by the sudden death of the animals. Pooled serum from tumor-bearing rats was fractioned on Sephadex G-150 and resulted in one peak that contained all of the antigenic activity. The molecular weight of this fraction was estimated to be 50,000 to 60,000 daltons. Presensitization of normal rats with soluble tumor antigens resulted in a specific acceleration of tumor growth and delay in tumor rejection. Specificity was shown by lack of C58(NT)D tumor enhancement in rats presensitized with serum containing tumor antigens from a syngeneic but antigenically unrelated WR-6 lymphoma. The biological significance of circulating soluble tumor antigen mediating specific immunosuppression against an immunogenic tumor is discussed.
在荷瘤大鼠血清中检测到循环可溶性肿瘤抗原。用同基因C58(NT)D Gross病毒诱导的淋巴瘤接种经亚致死剂量照射的W/Fu大鼠,作为肿瘤抗原的来源。通过特异性抑制同基因W/Fu抗C58(NT)D抗体对51Cr肿瘤靶细胞的补体介导的细胞毒性来评估可溶性抗原。皮下接种5×10(7)个肿瘤细胞后,在第8天首次检测到循环肿瘤抗原,到第13至14天达到最高浓度,这与肿瘤生长的峰值一致,随后动物突然死亡。将荷瘤大鼠的混合血清在Sephadex G - 150上进行分级分离,得到一个包含所有抗原活性的峰。该级分的分子量估计为50,000至60,000道尔顿。用可溶性肿瘤抗原对正常大鼠进行预致敏导致肿瘤生长的特异性加速和肿瘤排斥延迟。用含有来自同基因但抗原无关的WR - 6淋巴瘤的肿瘤抗原的血清预致敏的大鼠中缺乏C58(NT)D肿瘤增强,表明了特异性。讨论了循环可溶性肿瘤抗原介导针对免疫原性肿瘤的特异性免疫抑制的生物学意义。