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TV-5010在炎症性肠病小鼠模型——葡聚糖诱导的结肠炎中的治疗效果。

The therapeutic effect of TV-5010 in a murine model of inflammatory bowel disease -- Dextran induced colitis.

作者信息

Aharoni Rina, Brenner Ori, Cohen Adva, Arnon Ruth

机构信息

Department of Immunology, The Weizmann Institute of Science, Rehovot 76100, Israel.

出版信息

Int Immunopharmacol. 2008 Nov;8(11):1578-88. doi: 10.1016/j.intimp.2008.06.014. Epub 2008 Jul 26.

Abstract

TV-5010 is a higher molecular weight version of glatiramer acetate (GA), the active ingredient of Copaxone - an approved drug for the treatment of multiple sclerosis (MS). GA has been shown to ameliorate colitis in several experimental models when administered by daily injection. The present study aimed to explore the effect of TV-5010 in a murine model of inflammatory bowel disease (IBD) and the possibility for its administration in tapered frequency. As demonstrated here, TV-5010 ameliorated the various pathological manifestations of Dextran (DSS)-induced colitis, i.e. weight loss, intestinal bleeding and diarrhea, resulting in substantial reduction of disease activity, colonic damage and mortality. In contrast to GA, which was more effective when administered daily by injection of 2.0 mg/mouse, TV-5010 was most effective when administered once a week, at dose of 0.2-1.0 mg/mouse. TV-5010 treatment abrogated the characteristic inflammation in the diseased organ as demonstrated by reduction in the colonic mRNA expression of TNF-alpha, IFN-gamma and the Th1 transcription factor T-bet, as well as by augmentation of the regulatory cytokine TGF-beta. Injection of naive mice with TV-5010 generated lymphocyte population of the Th2/3 subtype that effectively reduced disease manifestations upon adoptive transfer to mice with DSS-colitis. Moreover, TV-5010-specific T-cells, either exogenously labeled or genetically marked, adoptively transferred to colitis-induced mice, localized in the inner layers of the injured colon and expressed TGF-beta in situ. Thus, TV-5010 is effective in the suppression of experimental colitis similarly to GA, with the advantage of less frequent administration, possibly via immunomodulation at the site of pathological damage.

摘要

TV-5010是醋酸格拉替雷(GA)的高分子量版本,醋酸格拉替雷是考帕松(Copaxone)的活性成分,考帕松是一种已获批准用于治疗多发性硬化症(MS)的药物。在多个实验模型中,每日注射GA已显示可改善结肠炎。本研究旨在探讨TV-5010在炎性肠病(IBD)小鼠模型中的作用及其采用递减给药频率给药的可能性。如本文所示,TV-5010改善了右旋糖酐(DSS)诱导的结肠炎的各种病理表现,即体重减轻、肠道出血和腹泻,从而大幅降低了疾病活动度、结肠损伤和死亡率。与每日注射2.0 mg/只小鼠时效果更佳的GA不同,TV-5010每周注射一次,剂量为0.2 - 1.0 mg/只小鼠时效果最佳。TV-5010治疗消除了患病器官中的特征性炎症,这表现为结肠中肿瘤坏死因子-α(TNF-α)、干扰素-γ(IFN-γ)和Th1转录因子T-bet的mRNA表达降低,以及调节性细胞因子转化生长因子-β(TGF-β)的增加。给未感染的小鼠注射TV-5010可产生Th2/3亚型的淋巴细胞群,将其过继转移到患有DSS结肠炎的小鼠体内时可有效减轻疾病表现。此外,外源性标记或基因标记的TV-5010特异性T细胞过继转移到结肠炎诱导的小鼠体内后,定位于受损结肠的内层并原位表达TGF-β。因此,TV-5010与GA一样,在抑制实验性结肠炎方面有效,且具有给药频率较低的优势,可能是通过在病理损伤部位进行免疫调节实现的。

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