Oral encapsulated transforming growth factor β1 reduces endogenous levels: Effect on inflammatory bowel disease.

Laura Hammer, Stacia Furtado, Edith Mathiowitz, Dominick L Auci
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引用次数: 3

Abstract

Background: TreXTAM® is a combination of the key regulatory cytokine transforming growth factor beta (TGFβ) and all trans retinoic acid (ATRA) microencapsulated for oral delivery to immune structures of the gut. It is in development as a novel treatment for inflammatory bowel disease (IBD).

Aim: To measure TGFβ levels in blood and tissue after oral administration of encapsulated TGFβ.

Methods: Animals were orally administered encapsulated TGFβ by gavage. Levels of drug substance in blood and in gut tissues at various times after administration were measured by ELISA.

Results: We made the surprising discovery that oral administration of TreXTAM dramatically (approximately 50%) and significantly (P = 0.025) reduced TGFβ levels in colon, but not small intestine or mesenteric lymph nodes. Similarly, levels in rat serum after 25 d of thrice weekly dosing with either TreXTAM, or microencapsulated TGFβ alone (denoted as TPX6001) were significantly (P < 0.01) reduced from baseline levels. When tested in the SCID mouse CD4+CD25- adoptive cell transfer (ACT) model of IBD, oral TPX6001 alone provided only a transient benefit in terms of reduced weight loss.

Conclusion: These observations suggest a negative feedback mechanism in the gut whereby local delivery of TGFβ results in reduced local and systemic levels of the active form of TGFβ. Our findings suggest potential clinical implications for use of encapsulated TGFβ, perhaps in the context of IBD and/or other instances of fibrosis and/or pathological TGFβ signaling.

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口服胶囊化转化生长因子β1降低内源性水平:对炎症性肠病的影响。
背景:TreXTAM®是一种关键调节细胞因子转化生长因子β (TGFβ)和全反式维甲酸(ATRA)微胶囊的组合,用于口服给药到肠道免疫结构。它是一种治疗炎症性肠病(IBD)的新方法。目的:测定口服tgf - β胶囊后血液和组织中tgf - β的水平。方法:采用灌胃法给药胶囊化TGFβ。用酶联免疫吸附法测定给药后不同时间血液和肠道组织中药物的含量。结果:我们令人惊讶地发现,口服TreXTAM显著(约50%)和显著(P = 0.025)降低了结肠中tgf - β水平,而不是小肠或肠系膜淋巴结。同样,每周给药三次TreXTAM或单独微胶囊TGFβ(标记为TPX6001) 25天后,大鼠血清中的水平与基线水平相比显著(P < 0.01)降低。当在SCID小鼠CD4+CD25-过继细胞转移(ACT) IBD模型中进行测试时,单独口服TPX6001仅在减轻体重方面提供了短暂的益处。结论:这些观察结果表明,肠道中存在负反馈机制,即局部递送tgf - β导致局部和全身活性形式tgf - β水平降低。我们的研究结果表明,在IBD和/或其他纤维化和/或病理性tgf - β信号传导的情况下,使用包封的tgf - β具有潜在的临床意义。
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