Leukocyte traffic control: a novel therapeutic strategy for inflammatory bowel disease

被引:8
作者
Fiorino, Gionata [1 ]
Correale, Carmen [1 ]
Fries, Walter [2 ]
Repici, Alessandro
Malesci, Alberto [3 ]
Danese, Silvio [1 ]
机构
[1] IRCCS Humanitas, Div Gastroenterol & Digest Endoscopy, IBD Unit, Milan, Italy
[2] Univ Messina, Messina, Italy
[3] Univ Milan, Milan, Italy
关键词
alpha; 4; beta; 7; adhesion; angiogenesis; CAM; Crohn's disease; inflammatory bowel disease; integrin; MAdCAM; molecules; natalizumab; ulcerative colitis; vedolizumab; PROGRESSIVE MULTIFOCAL LEUKOENCEPHALOPATHY; ACTIVE CROHNS-DISEASE; L-SELECTIN; P-SELECTIN; NATALIZUMAB; ANTIBODY; ADHESION; BINDING; MOLECULE; MICROVASCULATURE;
D O I
10.1586/ECI.10.40
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Inflammatory bowel bowel diseases share common pathogenetic mechanisms that are not yet completely understood. It is clear, however, that the expression and production of cytokines in response to inflammation plays a key role in mediating the migration of activated leukocytes. The process of angiogenesis and the expression of adhesion molecules on the intestinal microvasculature act as gateways, facilitating the recruitment of leukocytes into the gut mucosa. New agents specifically blocking adhesion molecules, in particular integrins, have been developed in order to limit the passage of activated leukocytes into the mucosa. Non-gut-specific anti-ntegrin agents, such as natalizumab, have been shown to be effective in the treatment of IBD, but the risk of serious adverse events has limited their further development. The development of a new specific molecule, vedolizumab, is currently under investigation in a large clinical trial. This novel specific anti-integrin drug seems to hold promise in the treatment of gut inflammation.
引用
收藏
页码:567 / 572
页数:6
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