Dalianis T, Ramqvist T, Klein G
Int J Cancer. 1984 Sep 15;34(3):403-6. doi: 10.1002/ijc.2910340318.
Mice and rats could be immunized against the polyoma-virus-induced tumor-specific transplantation antigen (TSTA) by repeated inoculation of frozen or irradiated cells of an MT-cDNA-transformed rat cell line (2.8) that contains only the polyoma middle T-antigen, or by cells that carried a host range mutant and expressed a full-length large T-antigen, but only non-functional N-terminal fragments of small and middle T. This shows that neither large T nor an intact middle T is necessary to elicit a polyoma tumor-specific graft rejection response. Either one of them is sufficient by itself.
通过反复接种仅含有多瘤病毒中间T抗原的MT - cDNA转化大鼠细胞系(2.8)的冷冻或辐照细胞,或接种携带宿主范围突变体并表达全长大T抗原但仅小T和中间T的无功能N端片段的细胞,可使小鼠和大鼠针对多瘤病毒诱导的肿瘤特异性移植抗原(TSTA)产生免疫。这表明引发多瘤肿瘤特异性移植排斥反应既不需要大T抗原也不需要完整的中间T抗原。它们中的任何一个本身就足够了。