Figure 3
Existence of HTLV-1–infected cells and ATL clones not only in TCM and TEM populations but also in the TSCM population. (A) Representative data of postsorting samples. Values indicate the purity of each sorted population. (B) The mean value of PVL in each population from HTLV-1 carriers and ATL patients are presented. Error bars indicate 1 standard deviation (SD) in triplicate. (C) Data described in (B) are summarized with box and whisker plots. The boxes represent the 25% to 75% percentiles, whiskers represent the range, and lines in the box represent the median values of the distribution. (D) Data of ATL clone–specific PCR using genomic DNA from 1 × 103 cells of each population are shown. Data from PBMCs of each patient or a HI are presented as positive controls or negative controls. The left lane shows the size marker.

Existence of HTLV-1–infected cells and ATL clones not only in TCM and TEM populations but also in the TSCM population. (A) Representative data of postsorting samples. Values indicate the purity of each sorted population. (B) The mean value of PVL in each population from HTLV-1 carriers and ATL patients are presented. Error bars indicate 1 standard deviation (SD) in triplicate. (C) Data described in (B) are summarized with box and whisker plots. The boxes represent the 25% to 75% percentiles, whiskers represent the range, and lines in the box represent the median values of the distribution. (D) Data of ATL clone–specific PCR using genomic DNA from 1 × 103 cells of each population are shown. Data from PBMCs of each patient or a HI are presented as positive controls or negative controls. The left lane shows the size marker.

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