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. 2015 Jul 16;4(7):e001932. doi: 10.1161/JAHA.115.001932

Table 2.

Numbers of Macrophages and T Lymphocytes in Natalizumab-Treated Animals and Controls

Immune Markers Early Late
Untreated (n=3) NZ (n=6) P Value Fold Decrease Untreated (n=6) NZ (n=4) P Value Fold Decrease
CD163 158.84 (±55.78) 47.36 (±18.77) * 3.35 282.45 (±36.97) 80.06 (±10.95) ** 3.53
CD68 84.34 (±16.67) 22.54 (±5.09) * 3.74 63.01 (±4.71) 52.87 (±10.83) * 1.19
MAC387 9.33 (±1.17) 7.43 (±3.19) ns 18.25 (±2.11) 15.91 (±7.46) ns
CD3 8.05 (±2.13) 5.13 (±3.02) ns 15.55 (±3.60) 12.27 (±5.42) ns
BrdU 9.31 (±1.57) 4.39 (±0.64) ns 21.19 (±5.85) 16.42 (±3.19) ns

Numbers represent the mean number of positive cells (cells/mm2)±SEM, in parentheses. All animals were SIV-infected and CD8-lymphocyte depleted, with 10 of the animals receiving natalizumab. Twenty random, nonoverlapping, ×200 fields of view were counted for each animal and the average number of positive cells/mm2 calculated. P values were calculated by comparing the mean number of positive cells for the indicated groups using the nonparametric Mann–Whitney t test

*

P<0.05

**

P<0.01). Fold change was calculated for the numbers of cells where there was a significant difference between the indicated groups. Early natalizumab-treated animals began treatment at the time of infection, 0 days postinfection (dpi). Late natalizumab-treated animals began treatment 28 dpi. All treated animals were treated weekly for 3 weeks with a dose of 30 mg/kg of α-VLA-4. BrdU indicates bromodeoxyuridine; ns, no significance; NZ, natalizumab treated.