T cell heterogeneity in asthma pathogenesis: from immunological mechanisms to biological targeted therapies.

Severe and overlapping asthma endotypes-particularly steroid-insensitive disease-remain undertreated, highlighting the need for a T-cell-centered synthesis. This review frames asthma heterogeneity through the interplay of T-cell axes, with Th2 pathways shaping T2-high disease and Th17/Treg imbalance characterizing T2-low features and much of steroid resistance. Building on this framework, we map therapies to mechanism: IL-4Rα and IL-5/IL-5R blockade chiefly mitigate Th2-dominated circuits, whereas upstream alarmin inhibition (e.g., TSLP) modulates epithelial-immune cues that influence both T2-high biology and selected T2-low processes. We then outline what is needed to translate mechanisms into decisions-integrated biomarkers to refine endotypes and mechanism-guided switching or combinations, with emphasis on T2-low populations where unmet need is greatest. By linking T-cell biology to therapeutic leverage points, the review offers a concise path from mechanism to patient stratification and more rational treatment choices.