Imaoka K, Yoshikawa Y, Kanai Y, Yamanouchi K
Laboratory Animal Research Center, University of Tokyo, Japan.
Arch Virol. 1988;102(1-2):111-8. doi: 10.1007/BF01315567.
Rabbits infected with the L strain of rinderpest virus (RV) produced high titres of antinuclear antibodies (ANA) which reached a maximum two weeks after inoculation but rapidly disappeared by 6-8 weeks. These ANAs reacted with HeLa cells by indirect immunofluorescence test resulting in a homogeneous nuclear fluorescence. In order to investigate the target antigens of ANAs, the effects on the nuclear fluorescence pattern of pretreating HeLa cells were examined: DNase 1 treatment resulted in a decrease in the fluorescence whereas no changes were evident after RNase A treatment. Some group of sera showed decreased fluorescence in the cells from which histones were acid extracted, but other groups did not change in fluorescence. Sera which had failed to react with acid extracted cells gave positive fluorescence following histone reconstitution. The results indicate that DNA and nucleohistone are the major target antigens for ANAs. In addition, antibodies against nucleoli and extractable nuclear antigens were induced in some rabbits.
感染牛瘟病毒(RV)L株的兔子产生了高滴度的抗核抗体(ANA),接种后两周达到峰值,但在6 - 8周时迅速消失。这些ANA通过间接免疫荧光试验与HeLa细胞反应,产生均匀的核荧光。为了研究ANA的靶抗原,检测了预处理HeLa细胞对核荧光模式的影响:DNA酶1处理导致荧光减弱,而RNA酶A处理后无明显变化。部分血清组在酸提取组蛋白的细胞中荧光减弱,但其他组荧光无变化。未与酸提取细胞反应的血清在组蛋白重构后产生阳性荧光。结果表明,DNA和核组蛋白是ANA的主要靶抗原。此外,部分兔子诱导产生了针对核仁及可提取核抗原的抗体。