Case report: distinctive immune abnormalities in a patient with procainamide-induced lupus and serositis

Am J Med Sci. 1992 Feb;303(2):99-104. doi: 10.1097/00000441-199202000-00007.

Abstract

To gain insight into the immunopathogenesis of drug-induced autoimmune disorders, lymphocyte and immunoglobulin distributions and cytokine levels were monitored in the peripheral blood and pleural fluid of a patient with procainamide-induced lupus and pleural effusion. Approximately 80% of the B cells in both compartments were CD5+ compared to 10% to 25% in normal adults. CD4/CD8 ratio and percentage CD4 were normal in peripheral blood. Serum levels of IgG (particularly IgG2), IL-6, and soluble IL-2R were slightly elevated, and those of IgA were significantly elevated compared to normal controls. Analysis of the pleural effusion revealed an increased CD4/CD8 ratio because of an increased percentage of CD4+CD29+ helper memory T cells, lack of expression of the resting B-cell marker CD21, immune complex deposition and complement consumption, increased relative levels of ANA, abnormally high levels of IL-6 and soluble IL-2R, and detectable levels of IL-1b, IFN-g and TNF-a. These observations provide evidence for the involvement of CD5+ B cells and differential helper T-cell activity in procainamide-induced lupus and for an association between local lymphocyte activation and organ pathology.

Publication types

  • Case Reports
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Aged
  • Antigens, CD / analysis
  • Autoimmune Diseases / chemically induced
  • Autoimmune Diseases / immunology
  • B-Lymphocytes / immunology
  • CD4 Antigens / analysis
  • CD5 Antigens
  • Cytokines / analysis*
  • Humans
  • Integrin beta1
  • Lupus Vulgaris / chemically induced*
  • Lupus Vulgaris / immunology
  • Lymphocytes / immunology*
  • Male
  • Procainamide / adverse effects*
  • Receptors, Interleukin-2 / analysis
  • Serositis / chemically induced*
  • Serositis / immunology

Substances

  • Antigens, CD
  • CD4 Antigens
  • CD5 Antigens
  • Cytokines
  • Integrin beta1
  • Receptors, Interleukin-2
  • Procainamide