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Blockade of lymphocyte trafficking in inflammatory bowel diseases therapy: importance of specificity of endothelial target

期刊

EXPERT REVIEW OF CLINICAL IMMUNOLOGY
卷 10, 期 7, 页码 885-895

出版社

TAYLOR & FRANCIS LTD
DOI: 10.1586/1744666X.2014.917962

关键词

biological therapy; CAM; Crohn's disease; inflammatory bowel disease; integrins; monoclonal antibody; pathogenesis; ulcerative colitis

资金

  1. Schering-Plough
  2. Astra Zeneca
  3. Abbott Laboratories
  4. Novo Nordisk
  5. Takeda Millennium
  6. Danone
  7. Salix Pharmaceuticals
  8. Pfizer
  9. UCB Pharma
  10. UCB Pharma, Ferring
  11. Vifor
  12. Merck Sharp Dohme
  13. AbbVie
  14. MSD
  15. Takeda
  16. Janssen
  17. UCB
  18. Merck Co, Inc.

向作者/读者索取更多资源

Inflammatory bowel diseases (IBD) are chronic, relapsing to continuously active inflammatory disorders of the gastrointestinal tract, of potentially destructive nature. So far, the excessive and/or unbalanced immune response has been the target of the majority of the IBD treatments. Despite the increasing use of immunosuppressants and anti-TNF- inhibitors, about 30% of patients with Crohn's disease and about one-tenth of patients with ulcerative colitis still require major abdominal surgery at 5-10 years. As a result, new therapeutic approaches are urgently needed. The endothelium has a key role in the development of the inflammation, as it selectively governs the leukocyte trafficking and the influx of leukocytes into the intestinal mucosa. Drugs blocking such crossing, specifically at intestinal level, are going to be a new therapeutic option in IBD.

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