Publication | Open Access
Mitochondrial functionality and metabolism in T cells from progressive multiple sclerosis patients
56
Citations
35
References
2019
Year
Clinical ImmunologyAdaptive Immune SystemT-regulatory CellImmunologyImmune RegulationImmune SystemT CellsImmune DysregulationMitochondrial FunctionalityNeurologyMetabolic SignalingNeuroimmunologyRegulatory T Cell BiologyAutoimmune DiseaseImmune SurveillanceAutoimmunityT Cell ImmunityImmune FunctionPrimary ProgressiveCell BiologyMitochondrial FunctionImmune Cell DevelopmentPhysiologyMitochondrial MedicineMultiple SclerosisCellular Immune ResponseMedicineCell Development
Abstract Patients with primary progressive (PP) and secondary progressive (SP) forms of multiple sclerosis (MS) exhibit a sustained increase in the number of Th1, T cytotoxic type‐1 and Th17 cells in peripheral blood, suggesting that the progressive phase is characterized by a permanent peripheral immune activation. As T cell functionality and activation are strictly connected to their metabolic profile, we investigated the mitochondrial functionality and metabolic changes of T cell subpopulations in a cohort of progressive MS patients. T cells from progressive patients were characterized by low proliferation and increase of terminally differentiated/exhausted cells. T cells from PP patients showed lower Oxygen Consumption Rate and Extracellular Acidification Rate, lower mitochondrial mass, membrane potential and respiration than those of SP patients, a downregulation of transcription factors supporting respiration and higher tendency to shift towards glycolysis upon stimulation. Furthermore, PP effector memory T cells were characterized by higher Glucose transporter ‐1 levels and a higher expression of glycolytic‐supporting genes if compared to SP patients. Overall, our data suggest that profound differences exist in the phenotypic and metabolic features of T cells from PP and SP patients, even though the two clinical phenotypes are considered part of the same disease spectrum.
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