Endoplasmic reticulum aminopeptidases in the pathogenesis of ankylosing spondylitis


Autoria(s): Kenna, Tony J.; Robinson, Philip C.; Haroon, Nigil
Data(s)

01/09/2015

Resumo

There has been significant progress in our understanding of the pathogenesis of AS. The advent of genome-wide association studies has increased the known loci associated with AS to more than 40. The endoplasmic reticulum resident aminopeptidases (ERAP) 1 and 2 were identified in this manner and are of particular interest. There appears to be a genetic as well as a functional interaction of ERAP1 and 2 with HLA-B27 based on the known functions of these molecules. Recent studies on the structure, immunological effects and the peptide-trimming properties of ERAP 1 and 2 have helped to provide insight into their pathogenic potential in AS. In this review, we explore the role of ERAP 1 and 2 in the pathogenesis of AS. © The Author 2015.

Identificador

http://eprints.qut.edu.au/94064/

Publicador

Oxford University Press

Relação

DOI:10.1093/rheumatology/kev218

Kenna, Tony J., Robinson, Philip C., & Haroon, Nigil (2015) Endoplasmic reticulum aminopeptidases in the pathogenesis of ankylosing spondylitis. Rheumatology, 54(9), pp. 1549-1556.

Direitos

Copyright 2015 The Authors

Fonte

Faculty of Health; Institute of Health and Biomedical Innovation

Palavras-Chave #Aminopeptidase #Endoplasmic reticulum #Endoplasmic reticulum resident aminopeptidase 1 #Endoplasmic reticulum resident aminopeptidase 2 #Misfolding #NK cell #Peptide #T cell response #Unfolded protein response #endoplasmic reticulum aminopeptidase 1 #endoplasmic reticulum aminopeptidase 2 #HLA B27 antigen #unclassified drug #ankylosing spondylitis #balancing selection #cell surface #dendritic cell #disease association #gene frequency #gene interaction #genetic association #haplotype #human #major histocompatibility complex #priority journal #Review #single nucleotide polymorphism
Tipo

Journal Article