T helper cell dysfunction in systemic lupus erythematosus (SLE) : relation to disease activity

• Published in: Journal of clinical immunology 1994-05, Vol.14 (3), p.169-177
• Main Authors: BERMAS, B. L, PETRI, M, GOLDMAN, D, MITTLEMAN, B, MILLER, M. W, STOCKS, N. I, VIA, C. S, SHEARER, G. M
• Format: Article
• Language: English
• Subjects: Adult; AIDS/HIV; Antigens, Viral - immunology; Biological and medical sciences; CD4-CD8 Ratio; Female; Humans; Influenza A virus - immunology; Interleukin-2 - biosynthesis; Isoantigens - immunology; Lupus Erythematosus, Systemic - immunology; Lupus Erythematosus, Systemic - pathology; Lymphocyte Activation - immunology; Male; Medical sciences; Phytohemagglutinins - immunology; Sarcoidosis. Granulomatous diseases of unproved etiology. Connective tissue diseases. Elastic tissue diseases. Vasculitis; T-Lymphocytes, Helper-Inducer - immunology; T-Lymphocytes, Helper-Inducer - pathology; Tetanus Toxoid - immunology
• ISSN: 0271-9142; 1573-2592
• DOI: 10.1007/BF01533366

Patients with systemic lupus erythematosus (SLE) are known to have defects in both humoral and cellular immunity. The significance of defective T cell-mediated immunity and its relationship to disease activity have not been clearly established. We studied in vitro T helper cell (Th) function in 150 SLE outpatients and correlated Th function with validated measures of disease activity. Interleukin 2 (IL-2) production by peripheral blood mononuclear cells (PBMC) was measured after stimulation with the recall antigens influenza A virus (FLU) and tetanus toxoid (TET), irradiated allogeneic peripheral blood mononuclear cells (ALLO), and phytohemagglutinin (PHA). We observed three patterns of Th response: (1) 76 of 150 (50%) of patients responded to the recall antigens FLU and/or TET, ALLO, and PHA; (2) 62 of 150 (42%) of patients did not respond to recall antigens but responded to ALLO and PHA; and (3) 12 of 150 (8%) of patients did not respond to either recall antigens or ALLO antigens. This diminished T cell function was correlated with higher disease activity as measured by four scales of clinical activity, such that individuals who exhibited more in vitro immune dysfunction presented with significant increases in their clinical activity indices. The alterations in T cell function could not be accounted for by medication doses alone. Thus, SLE patients have multiple distinct defects at the level of the Th cell which are associated with clinical measures of disease activity.