The Journal of Rheumatology · 2009 · 40 citations · 38 references
Life SciencesImmunologyMolecular GeneticsImmunopathologyInflammationInnate ImmunityDendritic Cell BiologyGenetic Susceptibility To AutoimmunityInnate Immune Gene PolymorphismsReceptor PolymorphismsToll-like Receptor GeneticsToll-like ReceptorsImmune Gene PolymorphismImmune Response Gene Polymorphism AnalysisToll-like Receptor 4 GeneticsToll-like Receptor Functional PolymorphismsToll-like Receptor Gene PolymorphismsToll-like Receptor LigandsToll-like Receptors In AutoimmunityToll-like Receptors In Inflammation
OBJECTIVE: Dendritic cells localized at the adventitia-media border of the normal medium-sized arteries play a pivotal role in the initiation of giant cell arteritis (GCA). These cells express a singular surface receptor profile, including a series of Toll-like receptors (TLR). Ligands of TLR-4 promote activation and differentiation of adventitial dendritic cells and are directly implicated in the pathogenesis of GCA. We aimed to assess the potential implication of the TLR4-(+896 A/G) gene polymorphism in the susceptibility to GCA. METHODS: A total of 210 patients diagnosed with biopsy-proven GCA and 678 matched controls were included in our study. DNA from patients and controls was obtained from peripheral blood. Samples were genotyped for the TLR4-(+896 A/G) (rs4986790) gene polymorphism by polymerase chain reaction, using a predesigned TaqMan allele discrimination assay. RESULTS: The TLR4 +896 G allele was significantly increased in biopsy-proven GCA patients compared to controls [p = 0.01; odds ratio (OR) 1.65; 95% confidence interval (CI) 1.08-2.52]. The increase was due to a significantly increased frequency of heterozygosity for the TLR4 -896 A/G genotype in the group of patients with biopsy-proven GCA compared to controls (TLR4 -896 A/G heterozygous in patients with GCA 18.1% compared to 11.4% in controls: p = 0.01; OR 1.72; 95% CI 1.10-2.69). However, no significant differences were observed when patients with GCA were stratified according to the presence of specific clinical features of the disease. CONCLUSION: Our results show for the first time an association of TLR4-(+896 A/G) gene polymorphism with susceptibility to biopsy-proven GCA.
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TLR4 mutations are associated with endotoxin hyporesponsiveness in humans
Nancy C. Arbour, Eva Lorenz, Brian C. Schutte et al. · Nature Genetics · 2000 · 2K citations
Life Sciences, Genetics, Immunology +10
Miguel Á. González‐Gay, Sônia Barros, Maria J. Lopez‐Diaz et al. · Medicine · 2005 · 323 citations
Vessel-Specific Toll-Like Receptor Profiles in Human Medium and Large Arteries
Olga Pryshchep, Wei Ma-Krupa, Brian R. Younge et al. · Circulation · 2008 · 318 citations · Full text
Life Sciences, Immunology, Pathology +17