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Issue 1110 coverAutoimmunity, Part B Novel Applications of Basic Research Volume 1110 published September 2007
Ann. N.Y. Acad. Sci. 1110: 382–388 (2007). doi: 10.1196/annals.1423.040
Copyright © 2007 by the New York Academy of Sciences
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Part II. Treatment

Targeting Vascular Adhesion Protein-1 to Treat Autoimmune and Inflammatory Diseases

DAVID J. SMITHa AND PETRI J. VAINIOa

a Biotie Therapies Corp., Turku, Finland

Key Words: vascular adhesion protein-1 (VAP-1) • copper-containing amine oxidase • semicarbazide-sensitive amine oxidase (SSAO) • adhesion molecule • leukocyte trafficking • inflammation • autoimmune disease

Address for correspondence: David Smith, Biotie Therapies Corp., Tykistökatu 6, Turku, FIN-20520, Finland. Voice: +358-22748922; fax: +358-22748910.  david.smith{at}biotie.com

The development of new, safe, and effective anti-inflammatory drugs represents a major challenge for the pharmaceutical industry, as well as a significant opportunity. The increasing prevalence of chronic inflammatory and autoimmune diseases associated with an aging population has led to an intense effort to discover new anti-inflammatory drug targets and drugs acting against them. This review highlights the recent progress made in developing therapies directed against an endothelial cell adhesion molecule called vascular adhesion protein (VAP)-1 for the treatment of chronic inflammatory disease as well as highlighting other therapeutic opportunities offered by this vascular target.






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