Cytomegalovirus (CMV) reactivation is a frequent complication after allogeneic hematopoietic stem cell transplantation (aHSCT) and critically shapes immune reconstitution. However, the clonal and functional dynamics of T cell responses to CMV remain insufficiently defined. In this study, we combined longitudinal single-cell RNA sequencing with paired T cell receptor sequencing to track γδ and αβ T cell clones at clonal resolution across five post-transplant time points in patients with and without CMV reactivation. This integrative approach revealed marked, patient-specific expansion of non-Vγ9Vδ2 γδ T cell clones, particularly within Vδ1⁺ and Vδ3⁺ subsets, which was associated with differentiation toward cytotoxic and antiviral effector states characterized by IFN-γ and TNF-α expression. Conventional CD8⁺ αβ T cells showed comparatively modest clonal dynamics during CMV reactivation in this cohort. Longitudinal tracking of individual clonotypes demonstrated heterogeneous but recurrent trajectories, with expanding γδ T cell clones frequently acquiring antiviral and cytotoxic phenotypes following CMV reactivation. These findings highlight the adaptive-like behavior and functional plasticity of non-Vγ9Vδ2 γδ T cells and provide a high-resolution framework for studying antiviral immune responses during immune reconstitution. KEY MESSAGES: Single-cell sequencing enables clonal tracking of T cells during CMV reactivation. γδ T cells show patient-specific clonal expansion after CMV reactivation. Expanding γδ T cell clones acquire antiviral and cytotoxic phenotypes. Vγ9Vδ2 γδ T cells remain stable with limited clonal expansion. αβ T cells display limited clonal responses during CMV reactivation.
Keywords: Cytomegalovirus reactivation; TCR sequencing; non-Vγ9Vδ2 γδ T cells; scRNA-seq; γδ T cells.
© 2026. The Author(s).