McLain L, Dimmock N J
Department of Biological Sciences, University of Warwick, Coventry, U.K.
J Gen Virol. 1994 Jun;75 ( Pt 6):1457-60. doi: 10.1099/0022-1317-75-6-1457.
A quantal assay, based on syncytium formation in the human T cell leukaemia-derived C8166 cell line, was used to determine the kinetics of human immuno-deficiency virus type 1 (HIV-1) strain IIIB neutralization. Three rat monoclonal antibodies (MAbs) were used, under physiological conditions of temperature and antibody concentration. MAb ICR39.3b (IgG2b) neutralized virus with no lag period while the other two MAbs, ICR39.13g (IgG2b) and ICR41.1i (IgG2a), neutralized with lag periods of 5 min and 15 min respectively. It was calculated that the latter two MAbs mediated neutralization by about two and three molecules of IgG per virion respectively. The highest neutralization rate constant (for MAb ICR 41.1i) was over 300-fold less than that of MAbs specific for the haemagglutinin of the enveloped influenza virus type A and for poliovirus type 1.
基于人T细胞白血病衍生的C8166细胞系中的合胞体形成,采用定量分析来确定1型人类免疫缺陷病毒(HIV-1)IIIB株中和的动力学。在温度和抗体浓度的生理条件下,使用了三种大鼠单克隆抗体(MAb)。单克隆抗体ICR39.3b(IgG2b)中和病毒时无延迟期,而其他两种单克隆抗体ICR39.13g(IgG2b)和ICR41.1i(IgG2a)分别有5分钟和15分钟的延迟期。据计算,后两种单克隆抗体分别通过每病毒体约两个和三个IgG分子介导中和作用。最高的中和速率常数(针对单克隆抗体ICR41.1i)比针对甲型包膜流感病毒血凝素和1型脊髓灰质炎病毒的单克隆抗体低300多倍。