Mulé J J, Stanton T H, Hellström I, Hellström K E
Int J Cancer. 1981 Sep 15;28(3):353-9. doi: 10.1002/ijc.2910280315.
Spleen cells from mice bearing large methylcholanthrene (MCA)-induced sarcomas were injected intravenously into mice challenged in the hind footpads with heavily-irradiated cells from the same or a different sarcoma. As measured by [3H]-thymidine incorporation on day 5 or 6, cellular proliferation in the draining popliteal lymph nodes of these mice was significantly depressed as compared to control animals receiving normal spleen cells or medium intravenously. The suppression was found to be mediated by a Qa-1-positive, Thy-1 positive cell. It was relatively resistant to cyclophosphamide treatment (100 mg/kg). Furthermore, it had both antigen-specific and non-specific components. The findings are discussed in relation to a suppressor activator cell-suppressor acceptor cell pathway in the immunoregulation of tumor immunity.
将携带大剂量甲基胆蒽(MCA)诱导肉瘤的小鼠的脾细胞静脉注射到后足垫接受来自相同或不同肉瘤的重度照射细胞攻击的小鼠体内。通过在第5天或第6天掺入[3H] - 胸腺嘧啶核苷来测量,与静脉注射正常脾细胞或培养基的对照动物相比,这些小鼠引流的腘窝淋巴结中的细胞增殖明显受到抑制。发现这种抑制是由Qa - 1阳性、Thy - 1阳性细胞介导的。它对环磷酰胺治疗(100mg / kg)相对耐药。此外,它具有抗原特异性和非特异性成分。结合肿瘤免疫调节中的抑制激活细胞 - 抑制受体细胞途径对这些发现进行了讨论。