Targeting Adhesion Molecules as a Potential Mechanism of Action for Intravenous Immunoglobulin
Author(s) -
Varinder Gill,
Christopher J. Doig,
Derrice Knight,
Emma J Love,
Paul Kubes
Publication year - 2005
Publication title -
circulation
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 7.795
H-Index - 607
eISSN - 1524-4539
pISSN - 0009-7322
DOI - 10.1161/circulationaha.105.546150
Subject(s) - medicine , intravital microscopy , in vivo , selectin , immunology , integrin , antibody , immune system , cell adhesion molecule , endothelium , in vitro , pharmacology , inflammation , biology , receptor , microcirculation , biochemistry , microbiology and biotechnology
Intravenous immunoglobulin (IVIg) therapy has been shown to have therapeutic benefit in more than 50 inflammatory and immune-related diseases; however, the potential benefit of IVIg in cardiovascular disease is more limited, in part because our understanding of the mechanisms underlying the effects of IVIg in innate immunity is incomplete.
Accelerating Research
Robert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom
Address
John Eccles HouseRobert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom