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首页> 外文期刊>Current drug targets-The International journal for timely in-depth reviews on drug targets >Vedolizumab for the Treatment of IBD: A Selective Therapeutic Approach Targeting Pathogenic a4b7 Cells
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Vedolizumab for the Treatment of IBD: A Selective Therapeutic Approach Targeting Pathogenic a4b7 Cells

机译:维多珠单抗治疗IBD:针对致病性a4b7细胞的选择性治疗方法

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摘要

Inflammatory bowel diseases- (IBD) are characterized by a persistent recruitment of large quantities of leucocytes from the blood to the gut mucosa. Adhesion molecules, such as integrins and their ligands, are the main players in this complex process. Leucocyte traffic control using a specific integrin inhibitors, such as natalizumab, has been plagued by severe systemic effects. The alpha_4beta_7- integrin and its ligand, the MadCAM-1, have been of special interest, since they are found exclusively on the gut-homing lymphocyte subpopulations and in the intestinal mucosa respectively. It follows that inhibition of such molecules should offer gut-specific immunosuppression, without the systemic effects of aspecific in-tegrin-antagonists. We review the role of vedolizumab, a humanized antibody against the alpha_4beta_7 - integrin, in both ulcera-tive colitis (UC) and Crohn's disease (CD). Results from clinical trials show that vedolizumab is effective in the induction and maintenance of remission in active CD and UC and has a very good safety profile. These data allow to confidently prospect that vedolizumab will be an important therapeutic option in the future of IBD treatment.
机译:炎症性肠病(IBD)的特征是从血液到肠粘膜持续募集大量白细胞。粘附分子,例如整联蛋白及其配体,是这一复杂过程的主要参与者。使用特定整联蛋白抑制剂(如那他珠单抗)的白细胞交通控制受到严重的全身性影响。 alpha_4beta_7-整联蛋白及其配体MadCAM-1非常受关注,因为它们分别在肠道归巢的淋巴细胞亚群和肠粘膜中发现。因此,抑制此类分子应可提供肠道特异性免疫抑制作用,而无非特异性整联蛋白拮抗剂的全身作用。我们综述了维多珠单抗(一种针对α_4beta_7-整联蛋白的人源化抗体)在溃疡性结肠炎(UC)和克罗恩病(CD)中的作用。临床试验结果表明,维多珠单抗可有效诱导和维持活性CD和UC的缓解,并具有非常好的安全性。这些数据使人们有信心地预测,维多珠单抗将是未来IBD治疗的重要治疗选择。

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