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Permanent URL to this publication: http://dx.doi.org/10.5167/uzh-18972

Huber, L C; Jüngel, A; Gay, S (2009). Targeting the epigenetic modifications of synovial cells. In: Tak, P P. New Therapeutic Targets in Rheumatoid Arthritis. Basel, Switzerland, 193-206. ISBN 978-3-7643-8237-7.

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Abstract

Rheumatoid arthritis (RA) is a systemic inflammatory disease that mainly affects the synovial tissues of joints. Like in other autoimmune-related disorders, both the etiology as well as the pathogenesis of RA has not yet been completely unravelled. It is generally accepted, though, that autoimmune disorders develop through a combination of the individual genetic susceptibility, environmental factors, and dysregulated immune responses.
Genetic predisposition has been described in RA, in particular as “shared epitope”, a distinct sequence of amino acids within the antigen presenting peptide groove of the major histocompatibility complex (MHC). Imbalanced immunity is reflected by the production of autoantibodies and the accumulation of reactive helper T cells within the rheumatoid synovium. In addition, environmental factors have been postulated as disease modulating agents, including smoking, nutrition and infectious agents. So far, these factors have been studied almost exclusively as separate agents.
However, the way genes are transcribed can be affected by environment, nutrition, and ageing – without changes in the nucleotide sequence of the underlying DNA. These patterns of alterations in the gene expression profiles are called epigenetics. The term epigenetics is used to refer to molecular processes that regulate gene expression patterns, however without changing the DNA nucleotide sequence. These epigenetic changes comprise the postsynthetical methylation of DNA and posttranscriptional modifications of histones, including methylation, phosphorylation, ubiquitination, sumoylation, biotinlyation and, most importantly, deacetylation and acetylation. With respect to the complex pathogenesis of rheumatic diseases, the epigenome is an emerging concept that integrates different etiologies and, thus, offers the opportunity for novel therapeutic strategies. Based on the fact that current therapies have not resulted in an ACR 70 above 60% and have never been targeting the activated synovial fibroblast, novel therapeutic strategies should target the epigenetic pathways of synovial activation in RA.

Item Type:Book Section, refereed, further contribution
Communities & Collections:04 Faculty of Medicine > Center for Integrative Human Physiology
04 Faculty of Medicine > University Hospital Zurich > Rheumatology Clinic and Institute of Physical Medicine
DDC:570 Life sciences; biology
610 Medicine & health
Language:English
Date:2009
Deposited On:03 Jun 2009 15:14
Last Modified:09 Jul 2012 05:48
Publisher:Birkhauser / Springer
Series Name:Progress in Inflammation Research
ISBN:978-3-7643-8237-7
Related URLs:http://www.springer.com/birkhauser/biosciences/book/978-3-7643-8237-7 (Publisher)
Citations:Google Scholar™

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