Published in Immunotherapy Weekly, May 26th, 2004
"Autoimmune T-helper cells drive pathogenic autoantibody production in systemic lupus erythematosus (SLE), but the mechanisms maintaining those T cells are unknown," scientists in Chicago explained. "Autoreactive T cells are normally eliminated by functional inactivation (anergy) and activation-induced cell death (AICD) or apoptosis through death receptor (Fas) signaling. However, mutations in the genes encoding Fas and its ligand (FasL) are rare in classical SLE4.
"By gene microarray profiling, validated by functional and biochemical studies," L.T. Xu and colleagues at Northwestern University...
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Source: Immunotherapy Weekly (2004-05-26)
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