<p>T helper 17 (Th17) cells are a heterogeneous subset of CD4⁺ T cells that mediate host defense and drive autoimmune pathology. While phosphorylation of STAT3 at tyrosine 705 (Y705) is essential for Th17 differentiation, the functional role of serine 727 (S727) phosphorylation remains unresolved. Here, we show that STAT3 S727 phosphorylation is selectively required for the differentiation and effector function of pathogenic Th17 (pTh17) cells. Mechanistically, S727 phosphorylation facilitates STAT3 interactions with transcriptional co-regulators and chromatin remodeling complexes, establishing a transcriptional and epigenetic landscape that reinforces pTh17 identity. A STAT3 S727A point mutation disrupts these interactions, resulting in aberrant STAT1 activation, elevated IFN-γ production, impaired glycolytic metabolism, and destabilization of the pTh17 program. Metabolomic and extracellular flux analyses revealed a marked reduction in glycolytic capacity and spare respiratory reserve in STAT3^S727A Th17 cells, indicating that S727 phosphorylation is required for optimal bioenergetic fitness and effector programming. In vivo, CD4⁺ T cells expressing STAT3^S727A have reduced pathological capacity in the experimental autoimmune encephalomyelitis (EAE), conferring protection in a murine model of multiple sclerosis. These findings uncover a noncanonical STAT3 signaling axis that integrates transcriptional and metabolic control of Th17-mediated neuroinflammation and suggest that selective targeting of S727 phosphorylation may offer therapeutic benefit in MS by disrupting both effector function and glycolytic support. One sentence summary. STAT3 S727 phosphorylation is essential for assembling transcriptional and metabolic programs that drive pathogenic Th17 differentiation and autoimmune neuroinflammation.</p>