| Literature DB >> 23031829 |
Chris Cotsapas1, David A Hafler.
Abstract
Recent genetic studies in multiple autoimmune and inflammatory diseases have identified hundreds of genomic loci harboring risk variants. These variants are shared between diseases at unexpectedly high rates, providing a molecular basis for the shared pathogenesis of immune-mediated disease. If properly used, these results could allow us to identify specific pathways underlying disease; explain disease heterogeneity by grouping patients by molecular causes rather than overall symptomatology; and develop more rational approaches to diagnosis and therapy targeting these molecular defects. Here we review the current state of play in the genetics of immune-mediated disease, evidence for this sharing and how this new knowledge can lead to medically actionable discoveries of pathobiology.Entities:
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Year: 2012 PMID: 23031829 DOI: 10.1016/j.it.2012.09.001
Source DB: PubMed Journal: Trends Immunol ISSN: 1471-4906 Impact factor: 16.687