Kouskoff V, Lacaud G, Nemazee D
Department of Pediatrics, Department of Medicine, National Jewish Medical and Research Center, 1400 Jackson Street, Denver, CO 80206, USA.
Science. 2000 Mar 31;287(5462):2501-3. doi: 10.1126/science.287.5462.2501.
Autoimmunity arises when immune tolerance to specific self-antigens is broken. The mechanisms leading to such a failure remain poorly understood. One hypothesis proposes that infectious agents or antigens can break B or T lymphocyte self-tolerance by expressing epitopes that mimic self. Using a transgenic immunoglobulin model, we show that challenge with self-mimicking foreign antigen rescues B cells from peripheral tolerance independent of T cell help, resulting in the accumulation of self-reactive cells in the lymph nodes and secretion of immunoglobulins that bind to a liver-expressed self-antigen. Therefore, our studies reveal a potentially important mechanism by which B lymphocytes can escape self-tolerance.
当对特定自身抗原的免疫耐受被打破时,自身免疫就会出现。导致这种失败的机制仍知之甚少。一种假说是,感染因子或抗原可以通过表达模拟自身的表位来打破B或T淋巴细胞的自身耐受。使用转基因免疫球蛋白模型,我们发现用模拟自身的外来抗原进行攻击可使B细胞从外周耐受中解脱出来,而无需T细胞的帮助,从而导致淋巴结中自身反应性细胞的积累以及与肝脏表达的自身抗原结合的免疫球蛋白的分泌。因此,我们的研究揭示了B淋巴细胞逃避自身耐受的一种潜在重要机制。