Figure 6
Figure 6. CDR3 spectratyping analysis of the TCR-δ chains in healthy adult donors and in patients after transplantation. Profiles of the CDR3 distribution of the Vδ1 (A), Vδ2 (B), and Vδ3 (C) subsets were generated from sorted CD4−CD8− cells from CMV+ (n = 13) and CMV− (n = 12) healthy donors. Longitudinal study of the γδ T-cell repertoire of the Vδ1, Vδ2, and Vδ3 subsets was carried out in patients during the first 12 months after SCT. (D) TCR Vγ8 chains profiles were generated from CMV+ (n = 19) and CMV− (n = 16) healthy donors. Results are presented as mean ± SD. N indicates healthy adult; Pt, patients; and 3/12, 6/12, and 12/12 indicate the 3-, 6-, and 12-month time points after transplantation, respectively. Samples were analyzed using nonparametric Mann-Whitney test, and P values were determined. P values less than .05 were considered significant.

CDR3 spectratyping analysis of the TCR-δ chains in healthy adult donors and in patients after transplantation. Profiles of the CDR3 distribution of the Vδ1 (A), Vδ2 (B), and Vδ3 (C) subsets were generated from sorted CD4CD8 cells from CMV+ (n = 13) and CMV (n = 12) healthy donors. Longitudinal study of the γδ T-cell repertoire of the Vδ1, Vδ2, and Vδ3 subsets was carried out in patients during the first 12 months after SCT. (D) TCR Vγ8 chains profiles were generated from CMV+ (n = 19) and CMV (n = 16) healthy donors. Results are presented as mean ± SD. N indicates healthy adult; Pt, patients; and 3/12, 6/12, and 12/12 indicate the 3-, 6-, and 12-month time points after transplantation, respectively. Samples were analyzed using nonparametric Mann-Whitney test, and P values were determined. P values less than .05 were considered significant.

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