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. 2008 Nov 5;83(2):572–583. doi: 10.1128/JVI.01715-08

FIG. 3.

FIG. 3.

T-lymphocyte apoptosis in peripheral LNs of SM and RM during acute SIV infection. (A) Percentage of active caspase-3-positive CD4+ and CD8+ T lymphocytes in LNs determined by flow cytometry. Means and standard errors of the means for SIVsmE041-infected SM (n = 2), SIVsmE041-infected RM (n = 4), and SIVmac239-infected RM (n = 6) shown. Asterisks denote P values of <0.01 as determined by the two-tailed unpaired t test. (B) Representative active caspase-3 IHC on LNs of one SIVsmE041-infected SM and one SIVmac239-infected RM before and 2 weeks after SIV infection. Caspase-3-positive cells (brown 3,3′-diaminobenzidine chromogen, indicated by the arrows) in the entire paracortical zone of the LN were counted and numbers were normalized relative to the entire LN section in mm2. Plasma SIV RNA values are shown in parentheses. All sections are at a magnification of ×200 with hematoxylin counterstaining. (C) Absolute numbers of active caspase-3-positive T lymphocytes in LNs before and after SIV infection. Asterisks denotes P values of <0.05 as determined by the two-tailed paired t test.