首页> 外文期刊>The Tohoku Journal of Experimental Medicine >Increased production of inflammatory cytokines in cultured CD4+ cells from patients with HTLV-I-associated myelopathy.
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Increased production of inflammatory cytokines in cultured CD4+ cells from patients with HTLV-I-associated myelopathy.

机译:HTLV-I相关性脊髓病患者培养的CD4 +细胞中炎性细胞因子的产生增加。

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摘要

We investigated the production of inflammatory cytokines derived from cultured T cells of peripheral blood lymphocytes (PBL) in 14 patients with HTLV-I-associated myelopathy (HAM). The production of inflammatory cytokines, such as tumor necrosis factor-alpha, interferon-gamma, and granulocyte-macrophage colony stimulating factor, was significantly increased in patients with HAM, compared to HTLV-I seronegative controls. On the contrary, interleukin-4 production in cultured T cells was detected in only two patients with HAM, and not detected in HTLV-I seronegative controls. These results suggest that the production of inflammatory cytokines derived from TH1 cell population was simultaneously exaggerated in HAM patients. Interestingly, accelerated production of these cytokines was derived from CD4+ cells, which are main target cells in HTLV-I infection. These findings suggest that an inflammatory state in the central nervous system might be related to the pathogenesis of HAM.
机译:我们调查了14例HTLV-I相关性脊髓病(HAM)患者的外周血淋巴细胞(PBL)培养的T细胞衍生的炎性细胞因子的产生。与HTLV-1血清阴性对照相比,HAM患者的炎症细胞因子(如肿瘤坏死因子-α,干扰素-γ和粒细胞-巨噬细胞集落刺激因子)的产生显着增加。相反,仅在两名HAM患者中检测到培养的T细胞中IL-4的产生,而在HTLV-1血清阴性对照中未检测到。这些结果表明,在HAM患者中,来自TH1细胞群的炎性细胞因子的产生同时被夸大了。有趣的是,这些细胞因子的加速产生源自CD4 +细胞,它们是HTLV-1感染的主要靶细胞。这些发现表明中枢神经系统的炎症状态可能与HAM的发病机制有关。

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