Geisbert Thomas W, Hensley Lisa E, Geisbert Joan B, Jahrling Peter B
Pathology Division, U.S. Army Medical Research Institute of Infectious Diseases, Fort Detrick, Maryland 21702-5011, USA.
Virology. 2002 Feb 1;293(1):15-9. doi: 10.1006/viro.2001.1279.
The neutralizing and enhancing activities of Ebola virus (EBOV)-specific antibodies were tested among four murine antibodies specific to the surface glycoprotein (GP), a recombinant human monoclonal antibody specific to GP, a polyclonal equine IgG, and serum obtained from a convalescent monkey. All but one of these antibodies neutralized EBOV infectivity of primary human monocytes/macrophages or Vero cells. None of the antibodies enhanced EBOV infectivity in these cells. Taken together with in vivo observations that early deaths were not observed in animals immunized with various viral vectors expressing EBOV GP, it is unlikely that any EBOV-enhancing antibodies profoundly affected EBOV pathogenesis.
在四种针对埃博拉病毒(EBOV)表面糖蛋白(GP)的鼠源抗体、一种针对GP的重组人单克隆抗体、一种多克隆马IgG以及一只康复猴的血清中,检测了EBOV特异性抗体的中和及增强活性。除一种抗体外,其他所有抗体均能中和原代人单核细胞/巨噬细胞或Vero细胞的EBOV感染性。这些抗体均未增强这些细胞中的EBOV感染性。结合体内观察结果,即用表达EBOV GP的各种病毒载体免疫的动物未观察到早期死亡,因此,任何EBOV增强抗体深刻影响EBOV发病机制的可能性不大。