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保护SJL/J小鼠免受泰勒氏鼠脑脊髓炎病毒介导的脱髓鞘疾病影响。

Protection of SJL/J mice from demyelinating disease mediated by Theiler's murine encephalomyelitis virus.

作者信息

Kurtz C I, Sun X M, Fujinami R S

机构信息

Department of Neurology, University of Utah School of Medicine, Salt Lake City 84132, USA.

出版信息

Microb Pathog. 1995 Jan;18(1):11-27. doi: 10.1016/s0882-4010(05)80009-9.

Abstract

Intracerebral infection with the DA strain of Theiler's murine encephalomyelitis virus induces a chronic demyelinating disease in SJL/J mice. Intraperitoneal inoculation with either the wild-type DA virus or an attenuated variant virus of DA, H7A6-2, results in protection from development of chronic demyelinating disease. Protective anti-viral immune responses result in reduced viral titers and decreased inflammation in the central nervous system within the first week following intracerebral challenge with virus. Development of protective immunity requires the presence of B cells and CD4+ T cells but does not require CD8+ T cells. High titers of serum anti-viral IgG and neutralizing antibodies are induced following the intraperitoneal inoculation with the DA virus or H7A6-2 virus prior to challenge. While protection could not be transferred with immune serum from DA virus-infected mice or neutralizing monoclonal antibodies, protection was correlated with increased numbers of DA virus-specific plasma cells in the central nervous system within the first week following intracerebral challenge. Protected mice also had enhanced levels of anti-DA virus IgG and neutralizing antibodies in the cerebral spinal fluid by 1 week following intracerebral challenge with DA virus. Thus, we conclude that vaccination with live virus results in protection from chronic demyelinating disease by inducing immune responses which are manifested in the central nervous system and rapidly clear infection after intracerebral challenge with DA virus.

摘要

用泰勒氏小鼠脑脊髓炎病毒DA株进行脑内感染可在SJL/J小鼠中诱发一种慢性脱髓鞘疾病。腹腔接种野生型DA病毒或DA的减毒变异病毒H7A6 - 2可预防慢性脱髓鞘疾病的发生。在脑内接种病毒后的第一周内,保护性抗病毒免疫反应可降低病毒滴度并减轻中枢神经系统的炎症。保护性免疫的发展需要B细胞和CD4 + T细胞的存在,但不需要CD8 + T细胞。在攻击前腹腔接种DA病毒或H7A6 - 2病毒后可诱导高滴度的血清抗病毒IgG和中和抗体。虽然来自DA病毒感染小鼠的免疫血清或中和单克隆抗体不能传递保护作用,但保护作用与脑内攻击后第一周内中枢神经系统中DA病毒特异性浆细胞数量的增加相关。在用DA病毒进行脑内攻击1周后,受保护小鼠的脑脊液中抗DA病毒IgG和中和抗体水平也有所提高。因此,我们得出结论,用活病毒进行疫苗接种可通过诱导免疫反应来预防慢性脱髓鞘疾病,这些免疫反应在中枢神经系统中表现出来,并在脑内接种DA病毒后迅速清除感染。

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