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Ribosomal P antibodies and CNS lupus.

Abstract
Within two years of the recognition of autoantibodies to ribosomal P proteins in patients with systemic lupus erythematosus (SLE) an association with anti-P autoantibodies with psychosis was noted. While there has been some controversy about this association, ample evidence suggests a meaningful relationship between anti-P antibodies and central nervous system (CNS) disease. This evidence consists of 1) seven independent studies showing a strong relationship between anti-P antibodies and CNS disease; 2) longitudinal studies showing fluctuations of anti-P antibodies with episodes of psychosis; 3) correlation of anti-P antibodies with general disease activity; and 4) acid eluates form lupus renal tissue were found to contain anti-P antibodies enriched 30-fold with respect to their specific activity in serum heralding a direct role of anti-P antibodies in disease expression. Finally, there is evidence that the P protein resides on normal cells in an immunologically accessible way and evidence exists that anti-P antibodies are able to bind and penerate cells in culture, and once inside cells can affect a profound inhibition of protein synthesis in living cells. Taken together, these observations provide evidence linking anti-P antibodies to various forms of CNS disease. While this is true, there are other autoantibodies in SLE patients such as anti-dsDNA and antiglial fibrillary protein which may also play a role in the CNS disease of SLE patients. Continued study will inform us of the relative contribution of these autoantibodies to CNS disease in SLE patients.
AuthorsM Reichlin
JournalLupus (Lupus) Vol. 12 Issue 12 Pg. 916-8 ( 2003) ISSN: 0961-2033 [Print] England
PMID14714911 (Publication Type: Comparative Study, Journal Article, Review)
Chemical References
  • Biomarkers
  • L12E protein, Trypanosoma cruzi
  • Protozoan Proteins
  • Ribosomal Proteins
Topics
  • Biomarkers (analysis)
  • Female
  • Humans
  • Lupus Vasculitis, Central Nervous System (cerebrospinal fluid, immunology, physiopathology)
  • Male
  • Prognosis
  • Protozoan Proteins
  • Ribosomal Proteins (analysis, immunology)
  • Risk Assessment
  • Sensitivity and Specificity
  • Severity of Illness Index

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