Antinuclear antibodies in rheumatic disease: a proposal for a function-based classification.

Journal Article (Journal Article;Review)

Antinuclear antibodies (ANAs) are a diverse group of autoantibodies that bind macromolecular components of the cell nucleus. While some ANAs occur in normal individuals, others are expressed almost exclusively in patients with rheumatic disease and serve as markers for diagnosis and prognosis. Despite the clinical associations of ANAs, the relationship of these antibodies to specific disease manifestations is often unknown because the target antigens are intracellular molecules that are ubiquitously expressed. In systemic lupus erythematosus, the role of ANAs in disease manifestations is better understood, especially for antibodies to DNA and related nucleosomal antigens. These antibodies can promote nephritis by the formation of immune complexes that are deposited in the kidney. In addition, anti-DNA, along with antibodies to RNA-binding proteins such as anti-Sm, can induce non-specific immune abnormalities based on the induction of type interferon 1 by plasmacytoid dendritic cells. Despite ANA expression in rheumatic disease, studies in animal models of inflammation and tissue injury indicate that antibodies to certain nuclear molecules such as HMGB1 have protective effects. Together, these considerations suggest a function-based classification of ANAs based on their expression in normal and autoimmune individuals as well as their capacity to induce or attenuate immunological disturbances. This classification provides a framework to elucidate the serological features of rheumatic disease and the often uncertain relationship between ANA expression and disease manifestations.

Full Text

Duke Authors

Cited Authors

  • Pisetsky, DS

Published Date

  • September 2012

Published In

Volume / Issue

  • 76 / 3

Start / End Page

  • 223 - 228

PubMed ID

  • 22670594

Electronic International Standard Serial Number (EISSN)

  • 1365-3083

Digital Object Identifier (DOI)

  • 10.1111/j.1365-3083.2012.02728.x


  • eng

Conference Location

  • England