Key result
Corticosteroid therapy in SLE links to normalized expression across most protein kinase C isoenzymes.
Observational
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We have studied the expressions of various protein kinase C (PKC) isoenzymes in T cells and monocytes from patients with systemic lupus erythematosus (SLE), in comparison to those of healthy controls and patients with other immunological disorders. As measured by Western blotting, the levels of PKCbeta, delta, eta, epsilon, theta and zeta (but not of PKCalpha) significantly decreased in T cells of SLE patients. In monocytes, however, we observed marked suppressions only in the expressions of PKCdelta, epsilon and zeta but not in the expressions of other PKC isoforms. In vivo corticosteroid application, as well as in vitro steroid treatment of monocytes, elevated the expressions of most isoforms close to normal values; however, the decreased levels of PKCtheta and zeta were not affected by steroid application. These alterations were characteristic to SLE because we could not detect any changes in the PKC levels in mononuclear cells of primary Sjögren's syndrome and mixed connective tissue disease patients. These results suggest that impaired PKC isoenzyme pattern may exist in the T cells and monocytes of SLE patients. Furthermore, the clinically efficient glucocorticoid application in SLE can increase the expression of some members of PKC system.
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Bı́ró et al. (2004) conducted an observational in Systemic lupus erythematosus (SLE). Corticosteroid application vs. Healthy controls and patients with primary Sjögren's syndrome and mixed connective tissue disease was evaluated on Expressions of protein kinase C (PKC) isoenzymes in T cells and monocytes. Corticosteroid application in SLE patients elevated decreased T-cell and monocyte expressions of most protein kinase C isoenzymes close to normal values, except PKCtheta and zeta.
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