Harvey J J, East J, Katz F E
Int J Cancer. 1979 Feb;23(2):217-23. doi: 10.1002/ijc.2910230213.
NZB mice injected intramuscularly throughout a 6-month period with the immunosuppressant azathioprine (Imuran) developed lymphocytic lymphomas 6--7 months after treatment was initiated. These malignancies were quite distinct from the reticulum-cell neoplasia which occurs spontaneously in the strain, and were readily transplantable to NZB or histocompatible BALB/c recipients. Xenotropic, but not ecotropic murine leukaemia virus (MuLV) was detected in leukaemic tissues of some donor and recipient NZBs when tested in vitro by co-cultivation with permissive cell lines, genome rescue, XC and viral polymerase assays. Virus filtrates prepared from donor leukaemic tissues were non-pathogenic when injected into newborn C3H mice. These results are evidence against a mandatory ecotropic MuLV genome in lymphocytic neoplasia.
在6个月的时间里,给NZB小鼠肌肉注射免疫抑制剂硫唑嘌呤(依木兰),在开始治疗6至7个月后,这些小鼠患上了淋巴细胞性淋巴瘤。这些恶性肿瘤与该品系自发发生的网状细胞肿瘤明显不同,并且很容易移植到NZB或组织相容性的BALB/c受体小鼠体内。当通过与允许性细胞系共培养、基因组拯救、XC和病毒聚合酶检测进行体外测试时,在一些供体和受体NZB的白血病组织中检测到了嗜异性而非亲嗜性小鼠白血病病毒(MuLV)。从供体白血病组织制备的病毒滤液注射到新生C3H小鼠体内时无致病性。这些结果证明淋巴细胞性肿瘤中不存在强制性的亲嗜性MuLV基因组。