Increased Fas and Bcl-2 expression on peripheral mononuclear cells from patients with active juvenile-onset systemic lupus erythematosus

J Rheumatol. 2007 Jul;34(7):1580-4. Epub 2007 May 15.

Abstract

Objective: To determine expressions of Fas and Bcl-2 on peripheral blood T and B lymphocytes from patients with juvenile-onset systemic lupus erythematosus (JSLE).

Methods: Thirty-eight patients with JSLE and 21 healthy controls were studied. Eleven JSLE patients with SLEDAI score >or= 8 were categorized as active. Freshly isolated peripheral blood mononuclear cells were stained for lymphocyte markers CD3, CD4, CD8, and CD19 and for Fas and Bcl-2 molecules. Cell protein expression was measured by 3-color flow cytometry.

Results: Percentages of lymphocytes positively stained for Fas antigen and cytoplasmic expression of Bcl-2 measured by mean fluorescence intensity from patients were significantly increased compared to controls on CD3+, CD4+, and CD8+ T cells. Patients with active disease had higher percentages of CD19+ B cells positive for Fas antigen compared to patients with inactive lupus. A direct statistical correlation was observed between Fas and Bcl-2 expression on CD19+ B cells and SLE Disease Activity Index score.

Conclusion: Patients with juvenile-onset SLE show upregulation of apoptosis-related proteins. Patients with active and inactive disease have a different profile of Fas and Bcl-2 expression.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adolescent
  • Adult
  • Age of Onset
  • Antigens, CD / metabolism
  • B-Lymphocytes / metabolism
  • B-Lymphocytes / pathology
  • Biomarkers / metabolism*
  • Cell Separation
  • Child
  • Disability Evaluation
  • Female
  • Flow Cytometry
  • Health Status
  • Humans
  • Leukocytes, Mononuclear / metabolism*
  • Leukocytes, Mononuclear / pathology
  • Lupus Erythematosus, Systemic / metabolism*
  • Lupus Erythematosus, Systemic / physiopathology
  • Male
  • Proto-Oncogene Proteins c-bcl-2 / metabolism*
  • Severity of Illness Index
  • T-Lymphocyte Subsets / metabolism
  • T-Lymphocyte Subsets / pathology
  • fas Receptor / metabolism*

Substances

  • Antigens, CD
  • Biomarkers
  • Proto-Oncogene Proteins c-bcl-2
  • fas Receptor