Yamamura Takashi
Department of Immunology, National Institute of Neuroscience, NCNP.
Nihon Rinsho. 2003 Aug;61(8):1329-34.
We have previously demonstrated that NK cells and CD1d-restricted NKT cells regulate clinical and pathological manifestations of experimental autoimmune encephalomyelitis(EAE), an animal model for multiple sclerosis(MS). It is important to address whether NK and NKT cells are also involved in the pathogenesis of human MS. Our laboratory has recently showed that NK cells as well as CD4+ NKT cells are biased for secreting type 2 cytokines in the remission phase of MS. However, CD4- CD8- NKT cells, that mainly secrete TNF-alpha and IFN-gamma, are reduced in number and attenuated in cytokine secretion. These results support our postulate that NK and NKT cells are involved in the regulation of MS.
我们之前已经证明,自然杀伤(NK)细胞和CD1d限制性自然杀伤T(NKT)细胞可调节实验性自身免疫性脑脊髓炎(EAE,一种多发性硬化症(MS)的动物模型)的临床和病理表现。探讨NK细胞和NKT细胞是否也参与人类MS的发病机制很重要。我们实验室最近发现,在MS缓解期,NK细胞以及CD4+ NKT细胞倾向于分泌2型细胞因子。然而,主要分泌肿瘤坏死因子-α(TNF-α)和干扰素-γ(IFN-γ)的CD4-CD8-NKT细胞数量减少,细胞因子分泌减弱。这些结果支持了我们关于NK细胞和NKT细胞参与MS调节的假设。