Eloit M, Fargeaud D, L'Haridon R, Toma B
Ministère de l'Agriculture, E.N.V., Maisons-Alfort, France.
Arch Virol. 1988;99(1-2):45-56. doi: 10.1007/BF01311022.
A total of 108 monoclonal antibodies specific for pseudorabies virus (PRV) were isolated in a cellular fusion, using spleen cells from mice which had been immunized with a live strain (Kojnok strain). Twelve of them neutralized the Kojnok strain in vitro in the absence of complement, as well as 28 virulent strains of various geographical origin and isolated from various animal species. All of the 12 clones were specific for glycoprotein gp50. Eighteen other clones with no neutralizing activity were studied: 11 reacted with glycoprotein GIII, 3 with glycoprotein GII, 3 with the glycoprotein gp63 and 1 with the glycoprotein GI. Transfer to mice of ascitic fluids corresponding to clones reacting with gp50 and GIII showed that some of them provided the mice with the ability of resisting to virulent challenge. Thus it appears that glycoproteins gp50 and GIII are major immunogens of the virion.
利用经活毒株(科伊诺克毒株)免疫的小鼠脾细胞进行细胞融合,共分离出108种针对伪狂犬病病毒(PRV)的单克隆抗体。其中12种在无补体的情况下能在体外中和科伊诺克毒株,以及28种来自不同地理区域、从不同动物物种分离出的强毒株。所有这12个克隆都对糖蛋白gp50具有特异性。另外研究了18个无中和活性的克隆:11个与糖蛋白GIII反应,3个与糖蛋白GII反应,3个与糖蛋白gp63反应,1个与糖蛋白GI反应。将与gp50和GIII反应的克隆对应的腹水转移到小鼠体内,结果显示其中一些使小鼠具备了抵抗强毒株攻击的能力。因此,糖蛋白gp50和GIII似乎是病毒粒子的主要免疫原。