Department of Microbiology, University of Alabama, Birmingham, Alabama, USA.
J Neurosci Res. 2010 Jan;88(1):1-6. doi: 10.1002/jnr.22176.
gammadelta T cells represent a small subpopulation of T cells expressing a restricted repertoire of T-cell receptors and, unlike alphabeta T cells, function more as cells of the innate immune system. These cells are found in skin and mucosal sites as well as secondary lymphoid tissues and frequently act as first line of defense sentinels. gammadelta T cells have been implicated in the pathogenesis of demyelinating disease, although little was known regarding their trafficking and effector functions. In this Mini-Review, we highlight recent studies demonstrating that gammadelta T cells migrate rapidly to the CNS during experimental autoimmune encephalomyelitis (EAE), the animal model for multiple sclerosis. gammadelta T-cell trafficking to the CNS is independent of beta(2)-integrins and occurs well before onset of clinical signs of disease, peaking early during the acute phase of disease. gammadelta T-cell-mediated production of inflammatory cytokines, including interferon-gamma and tumor necrosis factor-alpha, appears critical for EAE development, suggesting that these cells may set the stage for activation of other subsets of infiltrating effector cells. These data suggest that gammadelta T cells or subsets of gammadelta T cells may represent a new therapeutic target in demeylinating disease.
γδ T 细胞是 T 细胞的一个小亚群,其表达有限的 T 细胞受体库,与 αβ T 细胞不同,γδ T 细胞的功能更像是先天免疫系统的细胞。这些细胞存在于皮肤和黏膜部位以及次级淋巴组织中,通常充当第一道防御哨兵。γδ T 细胞被认为与脱髓鞘疾病的发病机制有关,尽管人们对其迁移和效应功能知之甚少。在这篇 Mini-Review 中,我们强调了最近的研究表明,在实验性自身免疫性脑脊髓炎(EAE)期间,γδ T 细胞迅速迁移到中枢神经系统,EAE 是多发性硬化症的动物模型。γδ T 细胞向中枢神经系统的迁移不依赖于β2-整合素,并且发生在疾病临床症状出现之前,在疾病的急性阶段达到高峰。γδ T 细胞介导的炎症细胞因子的产生,包括干扰素-γ和肿瘤坏死因子-α,对于 EAE 的发展似乎至关重要,这表明这些细胞可能为浸润效应细胞的其他亚群的激活奠定了基础。这些数据表明,γδ T 细胞或 γδ T 细胞亚群可能是脱髓鞘疾病的新治疗靶点。