Neumann Harald, Medana Isabelle M, Bauer Jan, Lassmann Hans
Neuroimmunology Unit, European Neuroscience Institute Göttingen, Waldweg 33, 37073 Göttingen, Germany.
Trends Neurosci. 2002 Jun;25(6):313-9. doi: 10.1016/s0166-2236(02)02154-9.
Cytotoxic T lymphocytes (CTLs) with a CD8(+) phenotype have the potential to recognize and attack major histocompatibility complex (MHC) class I-expressing brain cells. Most brain cells, including neurons, can be stimulated to present peptides to CD8(+) CTLs by MHC class I molecules, and are susceptible to CTL-mediated cytotoxicity in culture. In disease-affected brain parenchyma, CD8(+) CTLs outnumber other T-cell subtypes. They show clonal expansion in several inflammatory and degenerative CNS diseases, such as multiple sclerosis (MS), virus-induced inflammatory brain diseases and paraneoplastic neurological disorders. In MS, damage of axons is closely linked to the CD8(+) CTLs, and protection against CTL-mediated damage should be considered as a new therapeutic approach in MS and other neuroinflammatory diseases.
具有CD8(+)表型的细胞毒性T淋巴细胞(CTL)有识别并攻击表达主要组织相容性复合体(MHC)I类分子的脑细胞的潜力。大多数脑细胞,包括神经元,可被刺激通过MHC I类分子向CD8(+) CTL呈递肽段,并且在培养中易受CTL介导的细胞毒性作用影响。在疾病累及的脑实质中,CD8(+) CTL的数量超过其他T细胞亚型。它们在多种炎症性和退行性中枢神经系统疾病中呈现克隆性扩增,如多发性硬化症(MS)、病毒诱导的炎症性脑病和副肿瘤性神经系统疾病。在MS中,轴突损伤与CD8(+) CTL密切相关,针对CTL介导损伤的防护应被视为MS及其他神经炎症性疾病的一种新治疗方法。