口服克雷伯氏菌多糖AZ-9预防DBA/1小鼠胶原诱导的关节炎

Ryosuke Sugihara , Masayasu Yoshimura , Masaharu Mori , Naoki Kanayama , Masaki Hikida , Hitoshi Ohmori
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引用次数: 18

摘要

胶原诱导关节炎(CIA)是用牛II型胶原(CII)免疫DBA/1小鼠诱导的人类类风湿关节炎(RA)的优良模型。在这里,我们报道了通过口服AZ-9有效抑制CIA的诱导,AZ-9是一种纯化的多糖,平均分子量约为200 kDa,由土壤细菌克雷伯氏菌产生。在CII免疫后连续9天口服125-250 mg/kg/天AZ-9,然后每3天给药一次,可显著降低CIA的发生率和严重程度。az -9给药小鼠血清抗cii IgG2a水平和引流淋巴结(LN)细胞中IFN-γ和IL-12的产生明显低于未给药小鼠。这些发现表明,口服AZ-9通过减弱对CII的th1型反应来抑制CIA。AZ-9可以分裂成更小的分子(3-4 kDa)而不失去其抑制活性。
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Prevention of collagen-induced arthritis in DBA/1 mice by oral administration of AZ-9, a bacterial polysaccharide from Klebsiella oxytoca

Collagen-induced arthritis (CIA) is an excellent model of rheumatoid arthritis (RA) in humans that is induced in DBA/1 mice immunized with bovine type II collagen (CII). Here, we report that the induction of CIA was effectively suppressed by oral administration of AZ-9, a purified polysaccharide with the average molecular weight of approximately 200 kDa that was produced by a soil bacterium, Klebsiella oxytoca. When AZ-9 was administered at 125–250 mg/kg/day orally for 9 consecutive days after immunization with CII followed by its administration every 3 days, resulted in a marked reduction of the incidence and the severity of CIA. The serum level of anti-CII IgG2a and the production of IFN-γ and IL-12 in the draining lymph node (LN) cells were significantly lower in AZ-9-administered mice than the untreated control. These findings suggest that orally administered AZ-9 suppressed CIA through attenuating a Th1-type response to CII. AZ-9 could be fragmented into smaller molecules (3–4 kDa) without losing its suppressive activity.

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