Griffith I P, Crook N E, White D O
Br J Cancer. 1975 Jun;31(6):603-13. doi: 10.1038/bjc.1975.106.
The life span of C57/Bl mice inoculated with Lewis lung carcinoma cells was prolonged if the mice were pre-immunized with membranes from these cells infected in vitro with influenza virus. Likewise, BALB/c mice were protected against the malignant tumour WEHI-11 by prior immunization with extracts of cultured WEHI-11 cells which had been infected with influenza virus or Semiliki Forest virus (SFV). Partially purified SFV grown in WEHI-11 cells also protected mice from cancer grafts but neither highly purified SFV nor the glycoprotein from the envelope of this virus protected the mice. It is concluded that SFV-induced immunopotentiation against cancer is not due to covalent linkage of tumour specific transplantation antigen (TSTA) to viral envelope protein but more probably is due to the apposition of viral glycoprotein and cellular TSTA in the plasma membrane of the cancer cell.
如果用体外感染流感病毒的Lewis肺癌细胞膜对C57/Bl小鼠进行预先免疫接种,那么接种Lewis肺癌细胞的C57/Bl小鼠的寿命会延长。同样,通过预先用感染了流感病毒或Semiliki森林病毒(SFV)的培养的WEHI-11细胞提取物进行免疫接种,BALB/c小鼠对恶性肿瘤WEHI-11具有抵抗力。在WEHI-11细胞中生长的部分纯化的SFV也能保护小鼠免受癌移植,但高度纯化的SFV或该病毒包膜的糖蛋白均不能保护小鼠。得出的结论是,SFV诱导的抗癌免疫增强作用不是由于肿瘤特异性移植抗原(TSTA)与病毒包膜蛋白的共价连接,而更可能是由于病毒糖蛋白与癌细胞质膜中的细胞TSTA并列存在。