新的抗炎化合物FR167653下调人单核细胞和骨髓CD34+细胞向树突状细胞的分化和成熟

Naoki Nishimura, Yasuhiko Nishioka, Tsutomu Shinohara, Kenji Tani, Saburo Sone
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引用次数: 3

摘要

FR167653(1-[7-(4-氟苯基)-1,2,3,4-四氢-8(4-吡啶基)pyrazoro [5-1-c] [1], [2], [4] triazin-2-yl]-2-苯乙基硫酸二氢)是一种吡啶基咪唑类免疫抑制剂,是一种抑制促炎细胞因子产生的免疫抑制剂。我们研究了FR167653对人骨髓来源的树突状细胞(BM-DC)和血液单核细胞来源的DC (Mo-DC)分化和成熟阶段的影响。在FR167653存在的情况下,BM-DC或Mo-DC祖细胞诱导的DC均表达较低的CD1a、CD83和CD86 (B7.2)。FR167653还显著抑制了Mo-DC在LPS刺激下产生TNF-α和IL-1β的能力。FR167653对BM-DC的抑制作用要小得多,但FR167653对Mo-DC的混合淋巴细胞反应(MLR)刺激明显低于对照组。这些结果表明FR167653具有新的免疫抑制特性,可能通过下调DC分化和成熟来控制慢性免疫和/或炎症性疾病。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Down-regulation by a new anti-inflammatory compound, FR167653, of differentiation and maturation of human monocytes and bone marrow CD34+ cells to dendritic cells

FR167653 (1-[7-(4-fluorophenyl)-1,2,3,4-tetrahydro-8 (4-pyridyl) pyrazoro [5-1-c] [1], [2], [4] triazin-2-yl]-2-phenylethanedion sulfate monohydrate), one of the pyridinyl imidazoles, is an immunosuppressive agent which was developed to inhibit proinflammatory cytokine production. We examined the effect of FR167653 on the differentiation and maturation phases of both human bone marrow-derived dendritic cells (BM-DC) and blood monocyte-derived DC (Mo-DC). DC induced from either BM-DC or Mo-DC progenitors in the presence of FR167653 had lower expression of CD1a, CD83 and CD86 (B7.2). FR167653 also significantly suppressed the ability of Mo-DC to produce both TNF-α and IL-1β in response to LPS stimulation. Mixed lymphocyte reaction (MLR) stimulation was significantly lower in FR167653-treated Mo-DC than in control Mo-DC, although the suppressive effect of FR167653 was much less on BM-DC. These results indicate novel immunosuppressive properties of FR167653, which may be therapeutically useful in controlling chronic immune and/or inflammatory diseases through down-regulation of DC differentiation and maturation.

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