Lupus · 2006 · 33 citations · 7 references
Life SciencesImmunologyPharmacotherapyAutoimmunityImmunoregulationSignal TransductionAutoimmune DiseasesCorticosteroid TherapyCytokine BiologyImmune SignalingImmune-mediated Inflammatory DiseasesSystemic Lupus ErythematosusCell-mediated Immune DysfunctionCytokine Signaling In AutoimmunityDisease Activity MeasurementInflammatory T Cell ResponsesInterleukin RegulationRegulation Of T-cell ActivationSystemic Lupus Erythematosus AssociationsT Cell-mediated Inflammation
T cells from patients with systemic lupus erythematosus (SLE) have high levels of cAMP response element modulator (CREM)-alpha which bind to the interleukin (IL-2) promoter and limit IL-2 production. In this case-controlled study, we show that CREM-alpha mRNA levels were higher in T cells from patients with SLE than controls while CREB mRNA levels did not differ between the two groups. CREM-alpha mRNA levels did not correlate with clinical characteristics, disease activity or treatment. Nevertheless, there was a trend for patients on high doses of corticosteroids to have low levels of CREM-alpha mRNA. The discovery of specific non-toxic medications that block the expression of CREM-alpha may prove useful in reversing the aberrant T cell function in SLE.
7
Derivation of the sledai. A disease activity index for lupus patients
Claire Bombardier, Dafna D. Gladman, Murray B. Urowitz et al. · Arthritis & Rheumatism · 1992 · 4.6K citations
Alessandra Vacca, María Pía Felli, Antonietta R. Farina et al. · The Journal of Experimental Medicine · 1992 · 246 citations · Full text