Schuller-Petrovic S, Gebhart W, Lassmann H, Rumpold H, Kraft D
Nature. 1983;306(5939):179-81. doi: 10.1038/306179a0.
Considerable evidence for shared antigenic determinants between nervous elements and lymphocytes has accumulated. It has also been suggested that this cross-recognition may be involved in the pathogenesis of human neurological diseases such as myasthenia gravis and multiple sclerosis. We report here evidence that a marker for natural killer (NK) cells, anti-Leu-7 (HNK-1), specifically binds to components of human and rodent central nervous tissue as well as peripheral nervous tissue, especially to myelin sheaths. In contrast, another NK-cell marker (VEP13) did not react with nervous tissue. Since NK-cell function is impaired in a population of multiple sclerosis patients, the observed cross-reactivity indicates that autosensitization against myelin may simultaneously cause a defect of NK-cell function. Furthermore, the shared antigenic determinant may help to identify a hitherto undefined nervous tissue antigen and simultaneously increase the knowledge about the nature of NK-cell antigens.
关于神经元件与淋巴细胞之间共享抗原决定簇的大量证据已经积累起来。也有人提出,这种交叉识别可能参与了人类神经疾病如重症肌无力和多发性硬化症的发病机制。我们在此报告证据表明,自然杀伤(NK)细胞的一种标志物抗-Leu-7(HNK-1)特异性结合人和啮齿动物的中枢神经组织以及外周神经组织的成分,尤其是髓鞘。相比之下,另一种NK细胞标志物(VEP13)不与神经组织发生反应。由于在一部分多发性硬化症患者中NK细胞功能受损,观察到的交叉反应性表明,针对髓鞘的自身致敏可能同时导致NK细胞功能缺陷。此外,共享的抗原决定簇可能有助于识别一种迄今未明确的神经组织抗原,同时增加对NK细胞抗原性质的了解。