Shining a light on intestinal traffic.

Shining a light on intestinal traffic.
复制标题

DOI:
10.1155/2012/808157
复制
发表时间:
2012
影响因子:
--
通讯作者:
Melgar S
Melgar S
中科院分区:
其他
文献类型:
--
作者:
Murphy CT;Nally K;Shanahan F;Melgar S

文献摘要

参考文献

被引文献

相似文献

炎症性肠病(IBD),包括克罗恩病和溃疡性结肠炎,与肠道白细胞浸润增强有关,这与这些疾病的临床方面直接相关。因此,白细胞运输是IBD治疗的主要靶标。过去和新兴的技术,研究白细胞运输在体外和体内扩大了我们的知识,白细胞迁移过程和抑制剂的作用。已经采用了各种策略来靶向多步粘附级联和白细胞迁移中的S1 P/S1 PR 1轴内的趋化因子-和整合素-配体相互作用。虽然有大量的临床前数据证明白细胞运输抑制剂的疗效,但许多尚未在临床研究中得到证实。对IBD治疗的这一复杂和新兴领域需要警惕毒性和进一步研究。
Inflammatory bowel disease (IBD), encompassing Crohn's disease and ulcerative colitis, is associated with enhanced leukocyte infiltration to the gut, which is directly linked to the clinical aspects of these disorders. Thus, leukocyte trafficking is a major target for IBD therapy. Past and emerging techniques to study leukocyte trafficking both in vitro and in vivo have expanded our knowledge of the leukocyte migration process and the role of inhibitors. Various strategies have been employed to target chemokine- and integrin-ligand interactions within the multistep adhesion cascade and the S1P/S1PR1 axis in leukocyte migration. Though there is an abundance of preclinical data demonstrating efficacy of leukocyte trafficking inhibitors, many have yet to be confirmed in clinical studies. Vigilance for toxicity and further research is required into this complex and emerging area of IBD therapy.
DOI: 10.1034/j.1600-6143.2003.00130.x
发表时间: 2003-07-01
影响因子: 8.8
作者:
Budde, K;Schmouder, RL;Neumayer, HH
通讯作者: Neumayer, HH
DOI: 10.1084/jem.187.1.129
发表时间: 1998-01-05
影响因子: 15.3
作者:
Bonecchi, R;Bianchi, G;Bordignon, P P;D'Ambrosio, D;Lang, R;Borsatti, A;Sozzani, S;Allavena, P;Gray, P A;Mantovani, A;Sinigaglia, F
通讯作者: Sinigaglia, F
DOI: 10.1152/ajprenal.00311.2005
发表时间: 2006-06-01
影响因子: 4.2
作者:
Awad, AS;Ye, H;Okusa, MD
通讯作者: Okusa, MD
DOI: 10.1002/path.1245
发表时间: 2003-01-01
影响因子: 7.3
作者:
Banks, C;Bateman, A;Sheron, N
通讯作者: Sheron, N
DOI: 10.1046/j.1440-1827.2002.01365.x
发表时间: 2002-05-01
影响因子: 2.2
作者:
Arihiro, S;Ohtani, H;Nagura, H
通讯作者: Nagura, H