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Blood, Vol. 111, Issue 10, 5047-5053, May 15, 2008
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High frequency of CD4+FoxP3+ cells in HTLV-1 infection: inverse correlation with HTLV-1–specific CTL response
Blood Toulza et al. 111: 5047

Supplemental materials for: Toulza et al

Files in this Data Supplement:

  • Figure S1. Representation of the quantification of the rate of lysis for two HAM/TSP patients (JPG, 58.8 KB) -
    (A) The value in each quadrant represents the percentage of cells positive for the respective protein (Tax or FoxP3), gated on the CD4+ population, in the presence of an increasing frequency of CD8+ cells, after 18hr incubation. The quadrant marked “normal” represents the physiological point, with that patient’s normal percentage of CD8+ cells. The rate of lysis value () corresponding to the rate of Tax cell kill by CD8 by day. (B) Percentage of CD4 cells expressing Tax in 23 ACs and 22 HAM/TSP patients. Tax expression was assayed at the physiological ratio of CD4+:CD8+ cells (“normal”) after 18h incubation. (C) Density plot showing Tax and CD25 expression in PBMCs, gated on the CD4+ population, from a representative HAM/TSP patient (TAC) after 18h incubation.





  • Figure S2. Representation of the expression of CD4 and FoxP3 expression in the Tax population and FoxP3 expression in the Tax+ population (JPG, 16.8 KB) -
    The P value was calculated by an unpaired t-test (two-tailed). Each rate was calculated by the formula indicated.





  • Figure S3. Cytokine secretion detected by fluorescent microbead assay of PBMC supernatant (JPG, 57.9 KB) -
    (A) Data represent spontaneous cytokine production (pg/ml) in unstimulated peripheral blood mononuclear cells (PBMCs), incubated for 18h in vitro. Samples were taken from 5 uninfected controls, 12 asymptomatic HTLV-1 carriers, and 15 patients with HAM/TSP. P values were calculated using an unpaired t-test (two-tailed). Only significant differences are shown: * P< 0·05, ** P<0·005, *** P< 0·001. (B) Representation of two typical lysis assays (two HAM/TSP patients) with a high efficiency of lysis. In these two experiments we compared the rate of lysis in the presence or absence of 2 µg/ml of IL-10.





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