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Protective effect of small molecule analogues of the Acanthocheilonema viteae secreted product ES-62 on oxazolone-induced ear inflammation

机译:棘皮动物棘皮动物分泌产物ES-62的小分子类似物对恶唑酮诱导的耳部炎症的保护作用

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摘要

class="kwd-title">Keywords: ES-62, Immunomodulation, Oxazolone, Parasitic worm, Skin inflammation class="head no_bottom_margin" id="idm139620829085024title">AbstractES-62 is the major secreted protein of the rodent filarial nematode Acanthocheilonema viteae. The molecule contains covalently attached phosphorylcholine (PC) residues, which confer anti-inflammatory properties on ES-62, underpinning the idea that drugs based on this active moiety may have therapeutic potential in human diseases associated with aberrant inflammation. Here we demonstrate that two synthetic small molecule analogues (SMAs) of ES-62 termed SMA 11a and SMA 12b are protective in the oxazolone-induced acute allergic contact dermatitis mouse model of skin inflammation, as measured by a significant reduction in ear inflammation following their administration before oxazolone sensitisation and before oxazolone challenge. Furthermore, it was found that when tested, 12b was effective at reducing ear swelling even when first administered before challenge. Histological analysis of the ears showed elevated cellular infiltration and collagen deposition in oxazolone-treated mice both of which were reduced by treatment with the two SMAs. Likewise, the oxazolone-induced increase in IFNγ mRNA in the ears was reduced but no effect on other cytokines investigated was observed. Finally, no influence on the mast cell populations in the ear was observed.
机译:<!-fig ft0-> <!-fig @ position =“ anchor” mode =文章f4-> <!-fig mode =“ anchred” f5-> <!-fig / graphic | fig / alternatives / graphic mode =“ anchored” m1-> class =“ kwd-title”>关键字: ES-62,免疫调节,恶唑酮,寄生虫,皮肤炎症 class =“ head no_bottom_margin” id =“ idm139620829085024title”>摘要 ES-62是啮齿动物丝虫线虫棘突线虫的主要分泌蛋白。该分子包含共价连接的磷酸胆碱(PC)残基,赋予ES-62抗炎特性,从而巩固了基于这种活性部分的药物在与异常炎症相关的人类疾病中具有治疗潜力的想法。在这里,我们证明了ES-62的两个合成小分子类似物(SMAs),分别称为SMA 11a和SMA 12b,在恶唑酮诱导的皮肤过敏性急性过敏性接触性皮炎小鼠模型中具有保护作用,这是通过在小鼠炎症后耳部炎症的显着减少来衡量的在恶唑酮致敏之前和恶唑酮激发前给药。此外,发现在测试时,即使在挑战前首次给药,12b仍可有效减少耳肿。耳朵的组织学分析显示,在恶唑酮处理的小鼠中,细胞浸润和胶原蛋白沉积增加,而两种SMA均可降低这两种作用。同样,降低了恶唑酮诱导的耳朵中IFNγmRNA的增加,但未观察到对其他细胞因子的影响。最后,未观察到对耳朵中肥大细胞群体的影响。

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