Natalizumab for active Crohn's disease.
By Subrata Ghosh, E. Goldin, F. Gordon, H. Malchow, J. Rask-Madsen, P. Rutgeerts, P. Vyhnálek, Z. Zádorová, T. Palmer, S. Donoghue. New England Journal of Medicine, 2003
768 citations recorded by the source corpus.
Subfields: Epidemiology, Genetics, Immunology
View Paper: https://www.semanticscholar.org/paper/45a491b43b7318df857dd0ca0b749a7815eedcf7
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Citations in the corpus
- The neurobiology of multiple sclerosis: genes, inflammation, and neurodegeneration. (2006, neutral): “…(Yednock et al., 1992), clinical trials with Natalizumab , a humanized monoclonal antibody directed against the a4 integrin of the adhesion molecule VLA- 4, were conducted, and very encouraging results were reported in both MS (O'Connor et al., 2004) and Crohn's disease (Ghosh et al., 2003).”
- Immune cell migration in inflammation: present and future therapeutic targets (2005, background): “Furthermore, Natalizumab is very efficacious in Crohn diseas”
- The immunological and genetic basis of inflammatory bowel disease (2003, background): “In fact, treatment with antibodies specific for molecules that are involved in mucosal-specific migration, such as the integrin α4β7, has already been shown to have some therapeutic valu”
- Mechanisms of Disease: pathogenesis of Crohn's disease and ulcerative colitis (2006, background): “Monoclonal antibody to integrin-α 4 (natalizumab), which binds both intergrin-α 4 β 7 (the MAdCAM1 ligand) and integrin-α 4 β 1 (the VLA4 ligand), is effective in treating Crohn's disease”