肠道归巢分子调控炎症性肠病的发病机制及治疗。

Heather L Evans-Marin, Yingzi Cong
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引用次数: 1

摘要

炎症性肠病是一种慢性、使人衰弱的免疫系统疾病,目前几乎没有有效的治疗方法。针对肠道归巢分子的新疗法,如CCR9和α4β7,目前正在开发中,其中一些已经进入临床试验阶段。肠道营养分子及其受体对肠道耐受和炎症免疫反应的发展至关重要。然而,我们对归巢分子在IBD中的作用知之甚少。数据表明肠道归巢分子在IBD的发展和维持中具有病理和保护作用。此外,最近的研究发现,趋化因子可以影响T细胞的分化和功能。鉴于目前的临床相关性,有必要更好地了解肠道归巢分子在IBD调节中的作用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Gut Homing Molecule Regulation of the Pathogenesis and Treatment of Inflammatory Bowel Diseases.

Inflammatory bowel disease is a chronic, debilitating immunological disorder for which there are few effective treatments. New therapies targeting gut homing molecules, such as CCR9 and α4β7, are currently in development, with some of these reaching clinical trials. Gut-trophic molecules and their receptors are critical to the development of both tolerant and inflammatory immune responses in the gut. However, we know little regarding the function of homing molecules as it relates to IBD. Data have suggested both pathological and protective roles for gut homing molecules in IBD development and maintenance. In addition, recent research findings have suggested that chemokines can influence T cell differentiation and function. Given the current clinical relevance, it is essential to obtain a better understanding of the role of gut homing molecules in the regulation of IBD.

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