α2,6 sialylation distinguishes a novel active state in CD4+ and CD8+ cells during acute Toxoplasma gondii infection

Toxoplasmosis is a worldwide parasitosis that is usually asymptomatic; cell-mediated immunity, particularly T cells, is a crucial mediator of the immune response against this parasite. Membrane protein expression has been studied for a long time in T lymphocytes, providing vital information to determine functional checkpoints. However, less is known about the role of post-translational modifications in T cell function. Glycosylation plays essential roles during maturation and function; particularly, sialic acid modulation is determinant for accurate T cell regulation of processes like adhesion, cell-cell communication, and apoptosis induction. Despite its importance, the role of T cell sialylation during infection remains unclear. Herein, we aimed to evaluate whether different membrane sialylation motifs are modified in T cells during acute <i>Toxoplasma gondii</i> infection using different lectins. To this end, BALB/c Foxp3^EGFP mice were infected with <i>T. gondii</i>, and on days 3, 7, and 10 post-infection, splenocytes were obtained to analyze conventional (Foxp3^-) CD4⁺ and CD8⁺ populations by flow cytometry. Among the different lectins used for analysis, only <i>Sambucus nigra</i> lectin, which detects sialic acid α2,6 linkages, revealed two distinctive populations (SN^Bright and SN^-/Dim) after infection. Further characterization of CD4⁺ and CD8⁺ SN^-/Dim lymphocytes showed that these are highly activated cells, with a TEf/EM or TCM phenotype that produce high IFN-γ levels, a previously undescribed cell state. This work demonstrates that glycan membrane analysis in T cells reveals previously overlooked functional states by evaluating only protein expression.