4.6 Article

Metabolic Profiling of Rheumatoid Arthritis Neutrophils Reveals Altered Energy Metabolism That Is Not Affected by JAK Inhibition

期刊

METABOLITES
卷 12, 期 7, 页码 -

出版社

MDPI
DOI: 10.3390/metabo12070650

关键词

JAK inhibitors; metabolomics; NMR; rheumatoid arthritis; host defence; neutrophils; NETs

资金

  1. Pfizer Aspire IIR award [WI213850]
  2. Versus Arthritis and Masonic Charitable Fund PhD scholarship [22193]
  3. Wellcome Trust [200605/Z/16/Z]
  4. Versus Arthritis Career Development Fellowship [21430]
  5. University of Liverpool School of Life Sciences
  6. Wellcome Trust [200605/Z/16/Z] Funding Source: Wellcome Trust

向作者/读者索取更多资源

This study investigates the role of altered energy metabolism in neutrophils in rheumatoid arthritis and the effects of different JAK inhibitors on neutrophil metabolism. JAK inhibitors effectively inhibit ROS production and decrease NET production in neutrophils without impairing bacterial killing.
Neutrophils play a key role in the pathophysiology of rheumatoid arthritis (RA) where release of ROS and proteases directly causes damage to joints and tissues. Neutrophil function can be modulated by Janus Kinase (JAK) inhibitor drugs, including tofacitinib and baricitinib, which are clinically effective treatments for RA. However, clinical trials have reported increased infection rates and transient neutropenia during therapy. The subtle differences in the mode of action, efficacy and safety of JAK inhibitors have been the primary research topic of many clinical trials and systematic reviews, to provide a more precise and targeted treatment to patients. The aim of this study was to determine both the differences in the metabolome of neutrophils from healthy controls and people with RA, and the effect of different JAK inhibitors on the metabolome of healthy and RA neutrophils. Isolated neutrophils from healthy controls (HC) (n = 6) and people with RA (n = 7) were incubated with baricitinib, tofacitinib or a pan-JAK inhibitor (all 200 ng/mL) for 2 h. Metabolites were extracted, and H-1 nuclear magnetic resonance (NMR) was applied to study the metabolic changes. Multivariate analyses and machine learning models showed a divergent metabolic pattern in RA neutrophils compared to HC at 0 h (F1 score = 86.7%) driven by energy metabolites (ATP, ADP, GTP and glucose). No difference was observed in the neutrophil metabolome when treated with JAK inhibitors. However, JAK inhibitors significantly inhibited ROS production and baricitinib decreased NET production (p < 0.05). Bacterial killing was not impaired by JAK inhibitors, indicating that the effect of JAK inhibitors on neutrophils can inhibit joint damage in RA without impairing host defence. This study highlights altered energy metabolism in RA neutrophils which may explain the cause of their dysregulation in inflammatory disease.

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