Figure 1.
Figure 1. Accumulation of CD8+ T lymphocytes in the brain during HIVE. Increased number of CD8+ lymphocytes within the neuropil in HIVE brains (A) as compared with the seropositive patients without evidence of encephalitis (insert). Infiltrating CD8+ lymphocytes (purple) migrate toward HIV-1+ MPs (brown) of microglial nodule (B,C). The inset in panel A shows lymphocytes contained within the perivascular cuff in the HIV+ case. Human brain sections were double-immunostained with antibodies to CD8+ (purple, VIP substrate) and HIV-1 p24 (brown, DAB substrate). Original magnifications: panels A and B: ×100; panel C: ×200. (D) CD8+ lymphocytes were counted in basal ganglia and frontal cortex (white matter) of human brains (average of 10 consecutive 20 × fields). *P < .05 compared with HIV-seropositive and -seronegative controls. Error bars indicate standard error of the mean (SEM).

Accumulation of CD8+ T lymphocytes in the brain during HIVE. Increased number of CD8+ lymphocytes within the neuropil in HIVE brains (A) as compared with the seropositive patients without evidence of encephalitis (insert). Infiltrating CD8+ lymphocytes (purple) migrate toward HIV-1+ MPs (brown) of microglial nodule (B,C). The inset in panel A shows lymphocytes contained within the perivascular cuff in the HIV+ case. Human brain sections were double-immunostained with antibodies to CD8+ (purple, VIP substrate) and HIV-1 p24 (brown, DAB substrate). Original magnifications: panels A and B: ×100; panel C: ×200. (D) CD8+ lymphocytes were counted in basal ganglia and frontal cortex (white matter) of human brains (average of 10 consecutive 20 × fields). *P < .05 compared with HIV-seropositive and -seronegative controls. Error bars indicate standard error of the mean (SEM).

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