European Journal of Internal Medicine
Volume 20, Issue 8 , Pages 749-755, December 2009

Peptidylarginine deiminases and the pathogenesis of rheumatoid arthritis:

A reflection of the involvement of transglutaminase in coeliac disease

  • Pål Stenberg

      Affiliations

    • Lund University, Department of Clinical Sciences, Malmö, Clinical Coagulation Research Unit, Malmö University Hospital, S-205 02 Malmö, Sweden
    • Corresponding Author InformationCorresponding author. Tel.: +46 40 26 52 94; fax: +46 40 33 62 55.
  • ,
  • Bodil Roth

      Affiliations

    • Lund University, Department of Clinical Sciences, Malmö, Clinical Coagulation Research Unit, Malmö University Hospital, S-205 02 Malmö, Sweden
  • ,
  • Frank A. Wollheim

      Affiliations

    • Department of Rheumatology, Lund University Hospital, S-221 85 Lund, Sweden

Received 26 June 2009; received in revised form 17 August 2009; accepted 20 August 2009. published online 22 September 2009.

Abstract 

Post-translational modifications are associated with certain autoimmune diseases. For example, in the initial steps of coeliac disease (CD), transglutaminase type 2 (TG2) catalyzes a post-translational deamidation of specific glutamine residues in dietary gluten, resulting in antibodies against both modified gliadin and against TG2. Anti-TG2 has become a specific biomarker for CD. In rheumatoid arthritis (RA), the presence of antibodies against citrullinated peptides (ACPA) characterizes a distinct subset of this inflammatory disorder. Moreover, antibodies against the enzyme that catalyzes the citrullination (peptidylarginine deiminase; PAD) are found in RA. Their relation to disease severity indicates a possible pathogenetic role. Thus, in two major autoimmune diseases (CD and RA), antibodies are present against a post-translationally modified substrate and against the calcium-dependent thiol-enzyme (TG2 and PAD, respectively) responsible for the modification.

This review highlights the similarities between the TGs and the PADs and their putative pathogenetic roles in autoimmune diseases. Possible mechanisms of the effects of cigarette smoking and alcohol consumption on RA are discussed. By reflecting the progress in CD, the pathogenesis of ACPA-positive RA can be hypothesized where expression and regulation of PADs play significant roles. Indeed, autoimmune diseases should be studied collectively as well as individually. The new insight may lead towards innovative pharmacotherapeutic principles.

Abbreviations: ACPA, anti-citrullinated peptide antibody, CD, coeliac disease, DTT, dithiothreitol, EDTA, ethylenediaminetetraacetic acid, EMA, endomysial antibodies, FXIII, factor XIII, GAD, glutamic acid decarboxylase, MTX, methotrexate, PAD, peptidylarginine deiminase, pSS, primary Sjögren's syndrome, RA, rheumatoid arthritis, RF, rheumatoid factor, SE, shared epitopes, SLE, systemic lupus erythematosus

Keywords: Alcohol, Coeliac disease, Peptidylarginine deiminase, Rheumatoid arthritis, Smoking, Transglutaminase

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PII: S0953-6205(09)00165-4

doi:10.1016/j.ejim.2009.08.007

European Journal of Internal Medicine
Volume 20, Issue 8 , Pages 749-755, December 2009