Ebbesen P, Olsson L
J Cancer Res Clin Oncol. 1981;100(3):329-32. doi: 10.1007/BF00410694.
A revertant cell line, KSR-4111, cloned from a sarcoma virus transformed non-virus producing murine 3T3 cell line, K-BALB-23, was found to inhibit in vivo growth in newborn syngeneic mice of the transformed cells when grafted to the same locus, but not when grafted separately from the grafted tumor cells. No inhibition of outgrowth of the transformed K-BALB-23 cells was obtained with another revertant, KSR-12121, also cloned from the transformed K-BALB-23 cell, nor with the normal 3T3 cell. Furthermore, grafting of two syngeneic mammary tumors was unaffected by the presence of the protective revertant cells. The protective revertant KSR-4111 was furthermore characterized by inducing cytoxic non-theta-antigen-bearing spleen lymphocytes in grafted syngeneic recipients.
从肉瘤病毒转化的不产生病毒的小鼠3T3细胞系K - BALB - 23克隆出的回复细胞系KSR - 4111,当移植到同一位点时,被发现可抑制新生同基因小鼠体内转化细胞的生长,但与移植的肿瘤细胞分开移植时则无此作用。从转化的K - BALB - 23细胞克隆出的另一个回复细胞系KSR - 12121以及正常的3T3细胞,均未对转化的K - BALB - 23细胞的生长产生抑制作用。此外,两种同基因乳腺肿瘤的移植不受保护性回复细胞存在的影响。保护性回复细胞KSR - 4111的另一个特点是,可在移植的同基因受体中诱导产生携带细胞毒性非θ抗原的脾淋巴细胞。