Yefenof E, Meidav A, Kedar E
J Exp Med. 1980 Dec 1;152(6):1473-83. doi: 10.1084/jem.152.6.1473.
Adult C57BL/6 mice exposed to fractionated irradiation or inoculated with the radiation leukemia virus (RadLV), develop high incidence (80-100%) of lymphatic leukemias within 3-6 mo. RadLV-induced lymphomas can elicit cytotoxic responses in vitro in lymphocytes of preimmunized syngeneic mice, a reaction that is dependent on the expression of membrane-associated viral antigenicity. As soon as 5 d after RadLV inoculation, and during the entire leukemogenic process, suppressor T cells are detectable in the spleen that are capable of specifically abrogating generation of syngeneic anti-tumor cytotoxic cells in vitro. Mice exposed to fractionated x irradiation do not develop suppressor cells and their splenocytes may be stimulated in vitro to generate cytotoxicity toward RadLV-induced leukemias. These findings suggest that although RadLV has been isolated from radiation-induced leukemias, x-ray- and RadLV-induced leukemogenesis do not seem to involve a common viral etiology, and that induction of suppressor cells during RadLV leukemogenesis may be essential for tumor progression.
成年C57BL/6小鼠接受分次照射或接种辐射白血病病毒(RadLV)后,在3至6个月内会出现高发病率(80 - 100%)的淋巴细胞白血病。RadLV诱导的淋巴瘤可在预先免疫的同基因小鼠的淋巴细胞中引发体外细胞毒性反应,这种反应依赖于膜相关病毒抗原性的表达。在接种RadLV后5天以及整个白血病发生过程中,脾脏中可检测到抑制性T细胞,它们能够在体外特异性地消除同基因抗肿瘤细胞毒性细胞的产生。接受分次X射线照射的小鼠不会产生抑制性细胞,其脾细胞在体外可被刺激产生针对RadLV诱导的白血病的细胞毒性。这些发现表明,尽管RadLV已从辐射诱导的白血病中分离出来,但X射线和RadLV诱导的白血病发生似乎不涉及共同的病毒病因,并且RadLV白血病发生过程中抑制性细胞的诱导可能对肿瘤进展至关重要。