Progress in the genetics of ankylosing spondylitis


Autoria(s): Brown, Matthew A.
Data(s)

2011

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

http://eprints.qut.edu.au/87879/

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