Key result
The Su autoantigen complex, targeted by autoantibodies in systemic rheumatic diseases, contains key components of the RNA interference machinery, including Argonaute and Dicer proteins.
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The identification of RNA interference machinery components as targets of anti-Su autoantibodies provides new insights into the pathogenesis of systemic autoimmune diseases and potential links to viral infections.
Many intracellular macromolecular complexes that are involved in the production or degradation of RNAs are targeted by autoantibodies in systemic autoimmune diseases. RNA interference (RNAi) is a recently characterized gene silencing pathway by which specific mRNAs are either degraded or translationally suppressed. In a recent issue of Arthritis Research and Therapy, Andrew Jakymiw and colleagues reported that the enigmatic Su autoantigen complex contains key components of the RNAi machinery. Anti-Su autoantibodies from both human patients with rheumatic diseases and a mouse model of autoimmunity recognize the endonucleolytic Argonaute and Dicer proteins, both crucial enzymes of the RNAi pathway. These data raise the question of how the anti-Su response is triggered. So far, it is unknown whether molecular modifications may be involved, as has been proposed for other intracellular autoantigens. The implication of RNAi in anti-viral defence may suggest a role for virus infection in this process.
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Ger J.M. Pruijn (2006) conducted an editorial in Systemic autoimmune diseases. RNA interference pathway components (Su autoantigen) was evaluated. The Su autoantigen complex, targeted by autoantibodies in systemic rheumatic diseases, contains key components of the RNA interference machinery, including Argonaute and Dicer proteins.
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