Kitagawa M, Suzuki H, Adachi Y, Nakamura H, Yoshino S, Sumida T
Department of Internal Medicine, Institute of Clinical Medicine, University of Tsukuba, Ibaraki, Japan.
J Rheumatol. 2001 Aug;28(8):1764-71.
To determine the role of interferon-gamma (IFN-gamma) in CD40-CD154 dependent production of interleukin 12 (IL-12) by synovial cells of patients with rheumatoid arthritis (RA).
We examined the effects of IFN-gamma, tumor necrosis factor-alpha (TNF-alpha), and granulocyte-macrophage colony stimulating factor (GM-CSF) on CD40 expression on CD68+ synovial macrophage-lineage cells (SMC). The effects of IFN-gamma and soluble CD154 (sCD154) on IL-12 production by RA synovial cells were determined by ELISA.
CD68+ SMC expressed substantial levels of CD40. IFN-gamma, but not TNF-alpha or GM-CSF, markedly upregulated CD40 expression on CD68+ SMC. IFN-gamma also dose dependently increased IL-12 production by synovial cells. The effects of IFN-gamma on CD40 expression (EC50 = 127.4 U/ml) were observed at a concentration 19 times lower than the effects on IL-12 production (EC50 = 6.8 U/ml). Treatment with IFN-gamma at a concentration low enough to augment CD40 expression but not IL-12 production enhanced spontaneous IL-12 production synergy with sCD 154. The synergistic enhancement of spontaneous IL-12 production was abrogated by CD40-Fc. In contrast, IL-12 production induced by high concentration of IFN-gamma was not neutralized by CD40-Fc.
IFN-gamma enhanced IL-12 production via both CD40-CD154 dependent and independent pathways in RA synovium. IFN-gamma may play a crucial role in the development of RA synovitis through regulation of IL-12 production.
确定γ干扰素(IFN-γ)在类风湿关节炎(RA)患者滑膜细胞依赖CD40-CD154产生白细胞介素12(IL-12)过程中的作用。
我们研究了IFN-γ、肿瘤坏死因子-α(TNF-α)和粒细胞-巨噬细胞集落刺激因子(GM-CSF)对CD68+滑膜巨噬细胞系细胞(SMC)上CD40表达的影响。通过酶联免疫吸附测定法(ELISA)确定IFN-γ和可溶性CD154(sCD154)对RA滑膜细胞产生IL-12的影响。
CD68+ SMC表达大量水平的CD40。IFN-γ而非TNF-α或GM-CSF显著上调CD68+ SMC上的CD40表达。IFN-γ还剂量依赖性地增加滑膜细胞产生IL-12。IFN-γ对CD40表达的影响(半数有效浓度[EC50]=127.4 U/ml)在比其对IL-12产生影响(EC50 = 6.8 U/ml)低19倍的浓度下即可观察到。用浓度低到足以增强CD40表达但不增加IL-12产生的IFN-γ处理可增强与sCD154协同的自发性IL-12产生。CD40-Fc消除了自发性IL-12产生的协同增强作用。相反,高浓度IFN-γ诱导的IL-12产生未被CD40-Fc中和。
IFN-γ通过CD40-CD154依赖和非依赖途径增强RA滑膜中IL-12的产生。IFN-γ可能通过调节IL-12产生在RA滑膜炎的发展中起关键作用。