Medicine
Volume 38, Issue 2 , Pages 69-72, February 2010

Autoantibodies in the autoimmune rheumatic diseases

Richard Watts MA DM FRCP is Consultant Rheumatologist at Ipswich Hospital NHS Trust and Clinical Senior Lecturer at the University of East Anglia, UK. Competing interests: none declared

Abstract 

The detection of autoantibodies to a variety of antigenic targets plays an important role in the diagnosis of autoimmune rheumatic disease. Rheumatoid factor, antinuclear antibodies and antineutrophil cytoplasmic antibodies have been the key in the diagnosis of rheumatoid arthritis (RA), systemic lupus erythematosus and systemic vasculitis for many years. Antibodies against cyclic citrullinated peptides have been shown to be specific for rheumatoid arthritis and may predict the development of erosive disease, and are being increasingly used in the assessment of patients with RA. There is increasing interest in the use of anti-C1q antibodies for the detection and monitoring of lupus nephritis as this assay appears to be more sensitive than anti-DNA antibodies. Antibodies against β2-glycoprotein are being used more frequently as part of the diagnosis of the antiphospholipid antibody syndrome. Enzyme-linked immunosorbent assays are now being used in place of both radioimmunoassay and immunofluorescence because they are readily automated and less dependent on the use of experienced technicians.

Keywords: ANA, ANCA, anti-CCP antibodies, autoantibodies, ELISA, rheumatoid factor

To access this article, please choose from the options below

Login to an existing account or Register a new account.

  • Purchase this article for 31.50 USD (You must login/register to purchase this article)

    Online access for 24 hours. The PDF version can be downloaded as your permanent record.

  • Subscribe to this title

    Get unlimited online access to this article and all other articles in this title 24/7 for one year.

  • Claim access now

    For current subscribers with Society Membership or Account Number.

  • Visit SciVerse ScienceDirect to see if you have access via your institution.
 

PII: S1357-3039(09)00297-7

doi:10.1016/j.mpmed.2009.10.004

Medicine
Volume 38, Issue 2 , Pages 69-72, February 2010