Betton G R, Gorman N T
J Natl Cancer Inst. 1978 Oct;61(4):1085-93.
A series of 43 dogs with spontaneous melanomas, sarcomas, or mammary carcinomas were tested for peripheral blood lymphocytotoxicity against a range of allogeneic tumor cells in vitro on one or more occasions during therapy. All tumor-bearer groups contained a proportion of dogs showing a significant 51Cr release with increasing effector-to-target cell ratios. However, cytotoxicity was not restricted for target cells of the same histologic type as that of the effector cell donor. Some unrelated target cells more sensitive to nonspecific effects showed a greater cytotoxicity in some instances. Control effector cells from healthy dogs were nonspecifically cytotoxic for a range of tumor target cells in a similar proportion of instances. Short-term cultures of autochthonous tumor target cells were resistant to lysis in the 51Cr release assay. The findings did not provide evidence for the existence of specific tumor antigens operative to allogeneic 51Cr release cytotoxicity assays.
对43只患有自发性黑色素瘤、肉瘤或乳腺癌的犬进行了检测,在治疗期间的一次或多次体外试验中,检测其外周血淋巴细胞对一系列同种异体肿瘤细胞的细胞毒性。所有荷瘤犬组中都有一定比例的犬随着效应细胞与靶细胞比例的增加,出现显著的51铬释放。然而,细胞毒性并不局限于与效应细胞供体组织学类型相同的靶细胞。在某些情况下,一些对非特异性效应更敏感的无关靶细胞表现出更大的细胞毒性。来自健康犬的对照效应细胞在类似比例的情况下对一系列肿瘤靶细胞具有非特异性细胞毒性。在51铬释放试验中,自体肿瘤靶细胞的短期培养物对裂解具有抗性。这些发现没有为存在对同种异体51铬释放细胞毒性试验起作用的特异性肿瘤抗原提供证据。