NF-xB and STAT3 activation in CD4 T cells in pediatric MOG antibody-associated disease
JOURNAL OF NEUROIMMUNOLOGY(2023)
Abstract
In this study, we examined CD4 T cell activation using various stimuli in pediatric MOGAD patients (n = 4, untreated remission samples) and healthy controls (n = 5), to understand how both antigen-specific and bystander mechanisms contribute to CD4 T cell activation in MOGAD. TNF alpha, IL6, and MOG peptide pool were found to activate NF-xB or STAT3 pathways by measuring the expression of regulators (A20, IxB alpha) and phos-phorylated subunits (phospho-p65 and phospho-STAT3) using immunolabeling. Prednisolone reversed activation of both NF-xB and STAT3 and increased the expression of A20 and IxB alpha. TNFR blocking partially reversed NF-xB activation in certain CD4 T cell subsets, but did not effect STAT3 activation. We observed that activation of NF-xB and STAT3 in response to various stimuli behaves mostly same in MOGAD (remission) and HC. IL6 stimulation resulted in higher STAT3 phosphorylation in MOGAD patients at 75 min, specifically in central and effector memory CD4 T cells (with unadjusted p-values). These findings suggest the potential therapeutic targeting of NF-xB and STAT3 pathways in MOGAD. Further investigation is needed to validate the significance of extended STAT3 phosphorylation and its correlation with IL6 receptor blocker treatment response.
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Key words
MOGAD,STAT3,NF-xB,CD4,IL6,TNF alpha,A20,TNFR
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