Svoboda I, Măzuran R, Rabatić S
Int J Cancer. 1977 Mar 15;19(3):371-7. doi: 10.1002/ijc.2910190314.
Soluble preparations of antigens from a methylcholanthrene-induced fibrosarcoma of C57BI mice were prepared by homogenization of tumor tissue and high-speed centrifugation of the homogenate. These preparations were able to sensitize syngeneic mice to tumor-associated antigens (TAA) of the fibrosarcoma, and to provoke a delayed hypersensitivity reaction when injected into the footpad of sensitized mice. Furthermore, the same soluble preparations could inhibit in vitro the spreading of peritoneal macrophages from mice sensitized to TAA. A similar inhibition of macrophage spreading was obtained when peritoneal cells from C57BI mice, bearing transplants of the fibrosarcoma, were incubated with the preparations. We conclude that the macrophage spreading inhibition test, like other in vitro assays, can detect cell-mediated immunity to tumor-associated antigens.
通过将C57BI小鼠甲基胆蒽诱导的纤维肉瘤的肿瘤组织匀浆并对匀浆进行高速离心,制备了该纤维肉瘤抗原的可溶性制剂。这些制剂能够使同基因小鼠对纤维肉瘤的肿瘤相关抗原(TAA)致敏,并在注射到致敏小鼠的足垫时引发迟发型超敏反应。此外,相同的可溶性制剂可在体外抑制对TAA致敏的小鼠腹膜巨噬细胞的铺展。当将携带纤维肉瘤移植瘤的C57BI小鼠的腹膜细胞与这些制剂一起孵育时,也获得了类似的巨噬细胞铺展抑制效果。我们得出结论,巨噬细胞铺展抑制试验与其他体外试验一样,能够检测对肿瘤相关抗原的细胞介导免疫。