Rajcáni J, Hulíková Z, Mucha V
Acta Virol. 1979 Sep;23(5):403-11.
The binding of immune and preimmune rabbit sera to fixed VERO cells infected with herpes simplex virus type 1 (HSV 1) was measured by quantitative immunofluorescence. False positive binding of the preimmune serum (PS) occurred from 8 hr post infection (p.i.), while the immune serum (IS) revealed positive fluorescence starting with 4 hr p.i. The false binding of PS decreased significantly (P = 0.01) if the cells were cultured in the presence of 2-deoxy-D-glucose (DOG). Statistical analysis of data on the binding of IS to infected cells kept in the presence or absence of DOG showed that the mean values of immunofluorescence were not significantly different (P less than 0.1). Cells cultured for 8 hr p.i. in the presence of 6 mM DOG seem to be a suitable antigen for detection of the actual level of specific antibodies by indirect immunofluorescence.
通过定量免疫荧光法测定免疫兔血清和免疫前兔血清与感染1型单纯疱疹病毒(HSV 1)的固定VERO细胞的结合情况。免疫前血清(PS)在感染后8小时(p.i.)出现假阳性结合,而免疫血清(IS)在感染后4小时开始显示阳性荧光。如果细胞在2-脱氧-D-葡萄糖(DOG)存在的情况下培养,PS的假结合显著降低(P = 0.01)。对在有或无DOG存在的情况下保存的感染细胞上IS结合数据的统计分析表明,免疫荧光的平均值没有显著差异(P小于0.1)。在感染后8小时于6 mM DOG存在的情况下培养的细胞似乎是通过间接免疫荧光检测特异性抗体实际水平的合适抗原。