Figure 6
Figure 6. Changes in proliferating memory CD4+ T-cell subsets in neonatal tissues in pediatric SIV infection. (A) Very early, selective depletion of proliferating memory (BrdU+ CD95+) CD4+ T cells was consistently observed in the intestine of infected neonates by 3-7 days of infection. (B) After 21 days infection, massive loss of proliferating memory CD4+ T cells persists in all tissues examined. Flow cytometric plots indicate the distribution and frequency of proliferating (BrdU+, blue) cells in tissues having an activated (CD69+) and/or memory (CD95+) phenotype among all gated CD4+ T lymphocytes. Plots were gated through CD3+CD4+ lymphocytes. Data are expressed as means ± SE (*P < .05, **P < .01).

Changes in proliferating memory CD4+ T-cell subsets in neonatal tissues in pediatric SIV infection. (A) Very early, selective depletion of proliferating memory (BrdU+ CD95+) CD4+ T cells was consistently observed in the intestine of infected neonates by 3-7 days of infection. (B) After 21 days infection, massive loss of proliferating memory CD4+ T cells persists in all tissues examined. Flow cytometric plots indicate the distribution and frequency of proliferating (BrdU+, blue) cells in tissues having an activated (CD69+) and/or memory (CD95+) phenotype among all gated CD4+ T lymphocytes. Plots were gated through CD3+CD4+ lymphocytes. Data are expressed as means ± SE (*P < .05, **P < .01).

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