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Metabolic abnormalities and oxidative stress in lupus
Yaima L Lightfoot1, Luz P Blanco, Mariana J Kaplan
1Systemic Autoimmunity Branch, National Institute of Arthritis and Musculoskeletal and Skin Diseases, National Institutes of Health, Bethesda, Maryland, USA.
Current Opinion in Rheumatology
|June 23, 2017
Summary
Systemic lupus erythematosus (SLE) involves immune cell metabolic dysregulation and oxidative stress. Targeting these metabolic pathways and reducing mitochondrial reactive oxygen species (ROS) shows promise for treating lupus.
Area of Science:
- Immunology
- Metabolic pathways
- Oxidative stress
Background:
- Immune cell metabolism is crucial for effective immune responses.
- Metabolic checkpoint failures in autoimmunity can cause immune cell hyperactivation and tissue damage.
- Oxidative stress exacerbates immune dysregulation and host injury in autoimmune diseases.
Purpose of the Study:
- To review immune cell metabolism signatures in systemic lupus erythematosus (SLE).
- To discuss the impact of heightened oxidative stress in SLE patients.
- To explore potential therapeutic strategies targeting metabolic imbalances and oxidative stress.
Main Methods:
- Review of recent insights into immune cell metabolism in SLE.
- Analysis of the role of oxidative stress and mitochondrial reactive oxygen species (ROS).
- Evaluation of therapeutic interventions in experimental lupus models.
Main Results:
- Inhibitors of glucose metabolism, mTOR pathway modulators, and PPAR-γ agonists show therapeutic benefits in lupus models.
- Mitochondrial ROS and oxidative stress-induced modifications are detrimental in lupus.
- Therapies targeting metabolic reconfiguration and reducing mitochondrial ROS are under investigation.
Conclusions:
- Knowledge gaps exist regarding the metabolic requirements of key SLE immune cells like myeloid and B cells.
- SLE-specific metabolic signatures have been identified.
- Targeting these signatures and mitochondrial ROS holds therapeutic potential for SLE patients.
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