Smith A L, Cardellichio C B, Winograd D F, de Souza M S, Barthold S W, Holmes K V
Section of Comparative Medicine, Yale University School of Medicine, New Haven, CT 06510.
J Infect Dis. 1991 Apr;163(4):879-82. doi: 10.1093/infdis/163.4.879.
Because many strains of mouse hepatitis virus (MHV) infect laboratory mice, no effective vaccine has yet been developed. An alternative approach to control MHV disease is the use of a host cell receptor-targeted ligand. To address the potential usefulness of this approach, a monoclonal antibody directed against the host cell receptor for the coronavirus MHV-A59 was administered to infant mice that were then challenged oronasally with 10(4) intracerebral infant mouse median lethal doses of MHV-A59. Antibody treatment of virus-challenged mice resulted in lower proportions of mice with MHV-A59 in target organs and markedly reduced viral titers in these organs compared with mock-treated infected mice. Some antibody-treated infected mice survived for 7 days after viral challenge, whereas no mock-treated, infected mice survived beyond day 3 after viral inoculation. These results support a receptor-targeted approach to intervention in coronavirus disease.
由于多种小鼠肝炎病毒(MHV)毒株可感染实验小鼠,因此尚未开发出有效的疫苗。控制MHV疾病的另一种方法是使用靶向宿主细胞受体的配体。为了探究这种方法的潜在效用,将一种针对冠状病毒MHV-A59宿主细胞受体的单克隆抗体给予新生小鼠,随后这些小鼠经口鼻途径接受10⁴个脑内新生小鼠半数致死剂量的MHV-A59攻击。与模拟处理的感染小鼠相比,抗体处理病毒攻击小鼠后,靶器官中携带MHV-A59的小鼠比例降低,且这些器官中的病毒滴度显著降低。一些经抗体处理的感染小鼠在病毒攻击后存活了7天,而模拟处理的感染小鼠在病毒接种后第3天之后无一存活。这些结果支持了针对冠状病毒疾病的靶向受体干预方法。