Horwitz M S, Fine C, Ilic A, Sarvetnick N
Department of Immunology, The Scripps Research Institute, 10550 N. Torrey Pines Road, La Jolla, CA 92037, USA.
J Autoimmun. 2001 May;16(3):211-7. doi: 10.1006/jaut.2000.0486.
The induction of autoimmunity by viruses has been attributed to numerous mechanisms. Coxsackievirus B4 (CB4) induces insulin-dependent diabetes mellitus (IDDM) in mice resembling the final step of disease progression in humans. Following viral infection, autoreactive lymphocytes are activated through exposure to damaged islets consequently precipitating IDDM. However, the viral and host requirements leading up to this final step have yet to be elucidated. We provide evidence that disease induction requires a pre-existing accumulation of beta-cell specific autoreactive T cells within the pancreas, as well as the infection of islet beta-cells. Therefore, the primary role of CB4 in the development of IDDM is to infect tissue, resulting in the presentation of sequestered islet antigen, the stimulation of preexisting autoreactive T cells, and the initiation of disease.
病毒诱导自身免疫归因于多种机制。柯萨奇病毒B4(CB4)可在小鼠中诱发胰岛素依赖型糖尿病(IDDM),类似于人类疾病进展的最后阶段。病毒感染后,自身反应性淋巴细胞通过接触受损胰岛而被激活,从而引发IDDM。然而,导致这一最后阶段的病毒和宿主条件尚未阐明。我们提供的证据表明,疾病诱导需要胰腺内预先存在的β细胞特异性自身反应性T细胞的积累,以及胰岛β细胞的感染。因此,CB4在IDDM发展中的主要作用是感染组织,导致隔离的胰岛抗原呈递,刺激预先存在的自身反应性T细胞,并引发疾病。