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首页> 外文期刊>Annals of the New York Academy of Sciences >Molecular function of macrophage migration inhibitory factor and a novel therapy for inflammatory bowel disease
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Molecular function of macrophage migration inhibitory factor and a novel therapy for inflammatory bowel disease

机译:巨噬细胞迁移抑制因子的分子功能和炎性肠病的新疗法

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Macrophage migration inhibitory factor (MIF) is a unique protein that participates in inflammation, immune responses, and cell growth. An array of in vitro and in vivo experiments has demonstrated that MIF is profoundly involved in the pathogenesis of acute and chronic inflammatory disorders, such as inflammatory bowel disease (IBD). Blockade of MIF bioactivities by either neutralizing anti-MIF antibodies or antagonists prevents inflammatory cytokine cascade, which strongly suggests that an anti-MIF therapeutic strategy is feasible for treatment of IBD. Recently, we developed a new therapeutic approach for IBD by administration of antisense MIF oligonucleotides in conjugation with schizophyllan (SPG), a member of the glucan family. SPG specifically binds Dectin-1 expressed in antigen-presenting cells (APCs), and the antisense MIF/SPG complex is incorporated into the cells. In in vivo experiments of colitis models in mice, we found that intraperitoneal administration of the complex ameliorated the clinical signs of colitis and improved the histological scores. This novel therapy designed to knock down the MIF production in APCs is expected to be clinically applicable for the treatment of IBD.
机译:巨噬细胞迁移抑制因子(MIF)是参与炎症,免疫反应和细胞生长的独特蛋白质。一系列的体外和体内实验表明,MIF与急性和慢性炎症性疾病(如炎症性肠病(IBD))的发病机理密切相关。通过中和抗MIF抗体或拮抗剂来阻止MIF生物活性,可防止炎症性细胞因子级联反应,这强烈表明,抗MIF治疗策略对于治疗IBD是可行的。最近,我们通过将反义MIF寡核苷酸与葡聚糖家族成员裂果聚糖(SPG)结合使用,开发了一种新的IBD治疗方法。 SPG特异性结合在抗原呈递细胞(APC)中表达的Dectin-1,并且反义MIF / SPG复合物被掺入到细胞中。在小鼠结肠炎模型的体内实验中,我们发现腹膜内给药该复合物可改善结肠炎的临床体征并改善组织学评分。这种新颖的旨在降低APC中MIF产生的疗法有望在临床上用于IBD的治疗。

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