| Literature DB >> 18571006 |
Ralph D Levinson1, Zeying Du, Lihui Luo, Gary N Holland, Narsing A Rao, Elaine F Reed, Raja Rajalingam.
Abstract
Vogt-Koyanagi-Harada (VKH) disease is a putative autoimmune ocular inflammatory disease and is known to be associated with HLA-DR4 and -DR1 in Mestizos. We examined the genes encoding KIR receptors and human leukocyte antigen (HLA) class I ligands in patients with VKH disease and compared to published controls. We found trends toward more group B KIR haplogroups (p=0.059), with more activating KIR genes, in patients compared to controls. All putative activating KIR-HLA combinations were more common in patients, and some inhibitory KIR-HLA combinations were more common in controls, although the differences were not statistically significant. The trends observed in this study are consistent with those reported for other autoimmune diseases.Entities:
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Year: 2008 PMID: 18571006 DOI: 10.1016/j.humimm.2008.04.005
Source DB: PubMed Journal: Hum Immunol ISSN: 0198-8859 Impact factor: 2.850