甲基钴胺素(维生素B12)对外周血单核细胞体外细胞因子产生的影响。

M Yamashiki, A Nishimura, Y Kosaka
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引用次数: 0

摘要

最近在日本,一种维生素B12,甲基钴胺素,也被称为甲基B12,引起了医生们的注意,作为类风湿性关节炎患者的一种治疗方法。然而,其在体内的免疫作用尚不清楚。在这项研究中,我们通过添加不同的丝裂原(植物血凝素:PHA,豆豆蛋白A: ConA,或商陆丝裂原:PWM)和重组白介素-2,诱导白细胞介素-6 (IL-6)、干扰素- γ (ifn - γ)和白细胞介素-1 β (IL-1 β)等细胞因子的体外产生,并研究了甲基B12(终浓度为8-8,000 ng/ml)对外周血单核细胞产生这些细胞因子的影响。与对照组相比,在培养第4天,在培养基中添加甲基B12 (80-8,000 ng/ml)时,PHA和ConA诱导的IL-6产量平均被抑制60-70%。ifn - γ的产生与甲基B12呈剂量依赖性下降,即在rIL-2诱导下,ifn - γ的产生下降到对照的46%,在有丝分裂原诱导下,ifn - γ的产生下降到56-66%。在培养第1天,甲基B12对IL-1 β产生的影响较小。这些发现表明甲基B12主要抑制T淋巴细胞的细胞因子产生。这种体外抑制作用有望在类风湿性关节炎患者体内得到表达,尤其是在关节病变部位。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Effects of methylcobalamin (vitamin B12) on in vitro cytokine production of peripheral blood mononuclear cells.

Recently in Japan, one form of vitamin B12, methylcobalamin also known as methyl B12, has attracted the attention of physicians as a therapy for patients with rheumatoid arthritis. However, its immunological actions in vivo are still unknown. In this study, we induced the in vitro production of such cytokines as interleukin-6 (IL-6), interferon-gamma (IFN-gamma), and interleukin-1 beta (IL-1 beta) by adding various mitogens (phytohemagglutinin:PHA, concanavalin A: ConA, or pokeweed mitogen:PWM) as well as recombinant interleukin-2, and we investigated the effects of methyl B12 (final concentration, 8-8,000 ng/ml) on the production of these cytokines by peripheral mononuclear cells. As compared to the controls, IL-6 production induced by PHA and ConA on Day 4 of the culture was suppressed by an average 60-70% when methyl B12 (80-8,000 ng/ml) was added to the medium. IFN-gamma production decreased dose-dependently with methyl B12, i.e., it decreased to 46% of the control when this production was induced by rIL-2, and decreased to 56-66% when it was induced by mitogens. The effect of methyl B12 on IL-1 beta production on Day I of the culture was small. These findings indicate that methyl B12 suppresses mainly the cytokine production of T lymphocytes. Such suppressive effects as shown in the in vitro situation are expected to be expressed also in vivo in patients with rheumatoid arthritis, especially at articulation lesion sites.

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