Evermann J F, Burnstein T
Arch Virol. 1977;53(3):275-80. doi: 10.1007/BF01314673.
A persistent infection was established in a cell line derived from a hamster brain tumor (HBT) with the HBS strain of measles-subacute sclerosing panencephalitis (SSPE) virus. The persistently infected cells (HBT-M) were studied with regard to their growth in vitro and their transplantability in vivo. Although the growth of the HBT-M cells paralleled that of the HBT cells in vitro their transplantability was decreased in weanling hamsters. Hydrocortisone treatment of the hamsters abrogated the lowered transplantability restoring the tumor-producing capacity to levels comparable to the HBT cells. The decreased cell growth of the HBT-M cells in vivo was attributed to the acquisition of measles virus (MV) antigens and the host immune response directed against these new antigens.
用麻疹-亚急性硬化性全脑炎(SSPE)病毒的HBS株在源自仓鼠脑肿瘤(HBT)的细胞系中建立了持续性感染。对持续感染的细胞(HBT-M)进行了体外生长和体内移植能力的研究。虽然HBT-M细胞在体外的生长与HBT细胞相似,但在断奶仓鼠中其移植能力下降。用氢化可的松治疗仓鼠可消除移植能力的降低,使肿瘤产生能力恢复到与HBT细胞相当的水平。HBT-M细胞在体内生长的减少归因于麻疹病毒(MV)抗原的获得以及针对这些新抗原的宿主免疫反应。