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Figure 1.

Typical flow cytometric data for lymphocyte, CD4+ memory, and CD4+ naive cell populations.

At least 30,000 lymphocytes were evaluated and were gated based on their forward (FCS; X-axis) and side (SCS; Y-axis) scatter (Panels A&B). Memory and naive cell subpopulations were gated by positive surface staining for CD4 (Y-axis, panels C–F); memory cells were gated by positive surface staining for CD45RO (X-axis, panels C&D); naive cells were gated by positive surface staining for CD45RA (X-axis, panels E&F). Typical data from respective isotype controls (Panels A, C, and E) and fluorescently labeled samples (Panels B, D, and F) are shown.

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Figure 1 Expand

Table 1.

Characteristics of the MESA sample population being studied.

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Table 2.

Pearson correlation coefficients for CD4+ naive and memory cell subpopulations with biomarkers of inflammation, CVD risk, and infection.

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Table 2 Expand

Table 3.

Regression models for CD4+ naive and memory cell subpopulations.

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Table 3 Expand

Table 4.

Final regression model for coronary artery calcification.

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Table 5.

Final regression models for common carotid intimal media thickness in European-Americans.

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