Studies on human blood lymphocytes with iC3b (type 3) complement receptors: III. Abnormalities in patients with active systemic lupus erythematosus.

Abstract

Lymphocytes displaying iC3b (Type 3) complement receptors (CR3) were quantified by flow cytometry in patients with systemic lupus erythematosus. The percentages and absolute numbers were compared to age and sex matched controls. Total CR3+ lymphocytes identified by the monoclonal antibodies OKM1 or Leu 15 were significantly decreased in patients with symptomatic arthritis, serositis or vasculitis and those with lupus nephritis, whereas values for CR3+ lymphocytes in patients with inactive disease were similar to normal donors. The phenotype of CR3+ lymphocytes was markedly different in patients with active SLE. In normals granular lymphocytes bearing Fc receptors for IgG (L cells) comprised two-thirds of CR3+ lymphocytes. However, in SLE this subset was reduced to 20% and there was a corresponding increase in CR3+ lymphocytes co-expressing the T3 marker. Percentages of CR3 T4+ but not CR3+ T8+ lymphocytes were significantly increased in SLE. Although patients with active disease were lymphopenic, absolute numbers of CR3+ lymphocytes co-expressing T cell markers were similar to normal controls. Since L cells are non-specific suppressors of Ig production, the reduction of this subset along with the increase in CR3 T4+ cells could contribute to unregulated antibody production characteristic of SLE.

• Authors: J D Gray, A Lash, A C Bakke, R C Kitridou, D A Horwitz
• Journal: Clinical and experimental immunology (Clin Exp Immunol) Vol. 67 Issue 3 Pg. 556-64 (Mar 1987) ISSN: 0009-9104 [Print] England
• PMID: 2955974 (Publication Type: Journal Article, Research Support, Non-U.S. Gov't, Research Support, U.S. Gov't, P.H.S.)

Chemical References

• Antigens, Surface
• Receptors, Complement
• Receptors, Complement 3b
• Receptors, Fc
• Receptors, IgG
• Prednisone

Topics

• Adult
• Antigens, Surface (analysis)
• Female
• Humans
• Lupus Erythematosus, Systemic (immunology)
• Lymphocytes (classification, drug effects, immunology)
• Male
• Prednisone (pharmacology)
• Receptors, Complement (analysis)
• Receptors, Complement 3b
• Receptors, Fc (analysis)
• Receptors, IgG
• T-Lymphocytes (classification)