Figure 4
Unidirectional generation from HTLV-1–infected TSCM cells to TCM and TEM cells with rapid proliferation capacity. Data from culture of sorted TSCM, TCM, and TEM cells with 25 ng/mL recombinant human IL-7 and CFSE dilution for 2 weeks are presented. (A) FACS analyses of sorted samples in each case before in vitro culture. (B) FACS plots show sorted populations from a HI, HTLV-1 carriers, and ATL patients alter their phenotype. (C) The proportions of resulting phenotypic TSCM, TCM, and TEM cells shown in (B) are summarized. (D) The correlations of phenotypic alterations based on CD45RA level with proliferation ability are presented. The proliferation ability of each sorted population is assessed by the intensity of CFSE.

Unidirectional generation from HTLV-1–infected TSCM cells to TCM and TEM cells with rapid proliferation capacity. Data from culture of sorted TSCM, TCM, and TEM cells with 25 ng/mL recombinant human IL-7 and CFSE dilution for 2 weeks are presented. (A) FACS analyses of sorted samples in each case before in vitro culture. (B) FACS plots show sorted populations from a HI, HTLV-1 carriers, and ATL patients alter their phenotype. (C) The proportions of resulting phenotypic TSCM, TCM, and TEM cells shown in (B) are summarized. (D) The correlations of phenotypic alterations based on CD45RA level with proliferation ability are presented. The proliferation ability of each sorted population is assessed by the intensity of CFSE.

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