Fujinami R S, Rosenthal A, Lampert P W, Zurbriggen A, Yamada M
Department of Pathology, School of Medicine, University of California, San Diego, La Jolla 93093.
J Virol. 1989 May;63(5):2081-7. doi: 10.1128/JVI.63.5.2081-2087.1989.
Little or no antiviral immune response is mounted in athymic nude mice infected with the Daniels strain of Theiler's murine encephalomyelitis virus. In these athymic mice, increasing levels of infectious virus could be detected in the central nervous system. Seventy-five percent (9 of 12) of the nude mice were moribund or dead by 4 weeks postinfection. In contrast, treatment of Theiler's virus-infected nude mice with a neutralizing monoclonal antibody (H7-2) against the viral protein VP-1 resulted in a dramatic reduction of infectious virus within the central nervous system. All antibody-treated nude animals survived beyond 4 weeks postinfection. Monoclonal antibody titers could be maintained by passive transfer in treated nude mice at levels comparable to those of polyclonal antibody titers found in heterozygous infected nu/+ littermates. Areas of demyelination were detected in the untreated animals as early as 7 days after infection with little or no remyelination present. In approximately one-half of the antibody-treated nude animals, no demyelinating lesions were found. However, the rest of these treated mice were found to have areas of both demyelination and remyelination. Thus, anti-Theiler's murine encephalomyelitis virus antibody against VP-1 can play a dramatic role in the survival of mice, clearance of virus, limiting viral spread, and altering the pattern of disease in the absence of a functional T-cell response.
感染泰勒氏鼠脑脊髓炎病毒丹尼尔斯株的无胸腺裸鼠几乎没有产生抗病毒免疫反应。在这些无胸腺小鼠的中枢神经系统中,可以检测到传染性病毒水平不断升高。75%(12只中的9只)的裸鼠在感染后4周时濒死或死亡。相比之下,用针对病毒蛋白VP - 1的中和单克隆抗体(H7 - 2)治疗感染泰勒氏病毒的裸鼠,可使中枢神经系统内的传染性病毒显著减少。所有接受抗体治疗的裸鼠在感染后4周以上存活。通过被动转移,治疗后的裸鼠体内单克隆抗体滴度可维持在与杂合感染的nu/+同窝仔鼠中发现的多克隆抗体滴度相当的水平。在未治疗的动物中,早在感染后7天就检测到脱髓鞘区域,且几乎没有再髓鞘形成。在大约一半接受抗体治疗的裸鼠中,未发现脱髓鞘病变。然而,其余接受治疗的小鼠被发现既有脱髓鞘区域也有再髓鞘形成区域。因此,针对VP - 1的抗泰勒氏鼠脑脊髓炎病毒抗体在小鼠存活、病毒清除、限制病毒传播以及在缺乏功能性T细胞反应的情况下改变疾病模式方面可发挥显著作用。