Progress in the genetics of ankylosing spondylitis
Data(s) |
2011
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Resumo |
Ankylosing spondylitis (AS) is a common, highly heritable, inflammatory arthropathy. In addition to being strongly associated with HLA-B27, a further 13 genes have been robustly associated with the disease. These genes highlight the involvement of the IL-23 pathway in disease pathogenesis, and indicate overlaps between the pathogenesis of AS, and of inflammatory bowel disease. Genetic associations in B27-positive and -negative disease are similar, with the main exception of association with ERAP1, which is restricted in association to B27-positive cases. This restriction, and the known function of ERAP1 in peptide trimming prior to HLA Class I presentation, indicates that HLA-B27 is likely to operate in AS by a mechanism involving aberrant peptide handling. These advances point to several potential novel therapeutic approaches in AS. |
Identificador | |
Publicador |
Oxford University Press |
Relação |
DOI:10.1093/bfgp/elr023 Brown, Matthew A. (2011) Progress in the genetics of ankylosing spondylitis. Briefings in Functional Genomics, 10(5), pp. 249-257. |
Fonte |
School of Biomedical Sciences; Faculty of Health; Institute of Health and Biomedical Innovation |
Palavras-Chave | #Ankylosing spondylitis #Genome-wide association study #Heritable #SNP #Spondyloarthritis #HLA antigen class 1 #HLA B27 antigen #interleukin 23 receptor #transcription factor RUNX3 #tumor necrosis factor #article #DNA microarray #gene #genetic association #genetic linkage #genetic variability #genotype #human #pathogenesis #single nucleotide polymorphism #Humans #Major Histocompatibility Complex #Oligonucleotide Array Sequence Analysis #Spondylitis #Ankylosing |
Tipo |
Journal Article |