Figure 1.
Figure 1. Polychromatic profiling of the Vδ2 T-cell subsets. (A) 5-color flow cytometry discriminates between different subsets of naive and memory Vδ2 T cells from human PBMCs. Sequential gating using morphology and TCR expression defines noneffector and effector Vδ2+ cell subsets according to CD27 and CD62L expression, which are respectively subdivided according to expression of CD45RA and CD16. (B) After 6 hours of culture of PBMCs with phosphoantigen, intracellular staining for perforin and IFN-γ followed by 7-color flow cytometry as described in “Materials and methods” defines 2 functionally distinct subsets of effector memory Vδ2 T cells by showing that Vδ2TEMh are IFN-γ–producing lymphocytes with the TCRVδ2+CD27– CD62L–CD45RA– CD16– phenotype, whereas Vδ2TEMRA are perforin-producing lymphocytes with the TCRVδ2+CD27– CD62L–CD45RA+CD16+ phenotype. (C) Frequency of Vδ2TEMh and Vδ2TEMRA cells in PBMCs from 4 representative healthy donors and 2 cultured cell lines.

Polychromatic profiling of the Vδ2 T-cell subsets. (A) 5-color flow cytometry discriminates between different subsets of naive and memory Vδ2 T cells from human PBMCs. Sequential gating using morphology and TCR expression defines noneffector and effector Vδ2+ cell subsets according to CD27 and CD62L expression, which are respectively subdivided according to expression of CD45RA and CD16. (B) After 6 hours of culture of PBMCs with phosphoantigen, intracellular staining for perforin and IFN-γ followed by 7-color flow cytometry as described in “Materials and methods” defines 2 functionally distinct subsets of effector memory Vδ2 T cells by showing that Vδ2TEMh are IFN-γ–producing lymphocytes with the TCRVδ2+CD27 CD62LCD45RA CD16 phenotype, whereas Vδ2TEMRA are perforin-producing lymphocytes with the TCRVδ2+CD27 CD62LCD45RA+CD16+ phenotype. (C) Frequency of Vδ2TEMh and Vδ2TEMRA cells in PBMCs from 4 representative healthy donors and 2 cultured cell lines.

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