TNFα Regulates SIRT1 Cleavage during Ocular Autoimmune Disease

Elevated tumor necrosis factor (TNF) α levels are associated with chronic autoimmune diseases in which effects of TNFα on immune cells are multiple and complex. Analysis of uveitis in mice exhibiting severe autoimmune inflammation, resulting in a destructive subtotal loss of photoreceptors, revealed...

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Published inThe American journal of pathology Vol. 185; no. 5; pp. 1324 - 1333
Main Authors Gardner, Peter J, Yazid, Samia, Chu, Colin J, Copland, David A, Adamson, Peter, Dick, Andrew D, Calder, Virginia L
Format Journal Article
LanguageEnglish
Published United States Elsevier Inc 01.05.2015
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Summary:Elevated tumor necrosis factor (TNF) α levels are associated with chronic autoimmune diseases in which effects of TNFα on immune cells are multiple and complex. Analysis of uveitis in mice exhibiting severe autoimmune inflammation, resulting in a destructive subtotal loss of photoreceptors, revealed the presence of high plasma levels of TNFα and a significant population of CD4+ TNFα+ cells in the periphery and the eye at peak disease (TNFαhi ). We have shown previously by pharmacological activation that the deacetylase Sirtuin 1 (SIRT1) has an anti-inflammatory role in a less severe, TNFαlo model of uveitis. We now show that SIRT1 activation fails to clinically suppress severe TNFαhi disease, whereas glucocorticoid treatment is successful. TNFα has been reported to mediate cleavage and inactivation of SIRT1 during inflammation, and at peak disease we observed both full-length and cleaved SIRT1 in draining lymph node cells. In vivo systemic TNFα blockade suppressed severe ocular disease and restricted SIRT1 cleavage in the periphery, maintaining full-length active SIRT1 protein. When combining a suboptimal TNFα blockade with SIRT1 activation, a synergistic suppression of severe disease compared with TNFα blockade alone occurred. Our data suggest a new role for TNFα in exacerbating the severity of autoimmune disease by regulating SIRT1 cleavage in draining lymph node effector cells. SIRT1 activation may be effective as an adjunctive treatment for inflammatory conditions not fully controlled by TNFα inhibitors.
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ISSN:0002-9440
1525-2191
DOI:10.1016/j.ajpath.2015.01.017