| Literature DB >> 15630438 |
Abstract
For several decades, intravenous Ig has been used as treatment for a variety of immune-related diseases, including immune thrombocytopenic purpura (ITP), autoimmune neuropathies, systemic lupus erythematosus, myasthenia gravis, Guillain-Barré syndrome, skin blistering syndromes, and Kawasaki disease. Despite years of use, its mechanism of immunomodulation is still unclear. Recent studies using mouse models of ITP and arthritis, including one reported in this issue of the JCI, now provide some insights into this mechanism and the rationale for the development of Fcgamma receptor-targeted therapeutics.Entities:
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Year: 2005 PMID: 15630438 PMCID: PMC539209 DOI: 10.1172/JCI23994
Source DB: PubMed Journal: J Clin Invest ISSN: 0021-9738 Impact factor: 14.808