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1.
Figure 1

Figure 1. From: The impact of maternal HIV infection on cord blood lymphocyte subsets and cytokine profile in exposed non-infected newborns.

Analysis of B-cell maturation in cord blood of a normal newborn (control group). Expression of CD34 was used to identify immature B-cells. Maturation was studied using the expression of CD45, CD22, CD10 and membrane IgM (sIgM). A) CD45/CD34/CD19/CD22 combination - black: immature cells - CD45lowCD34+CD19+CD22- red: intermediate cells - CD45-/+CD34lowCD19+CD22+ yellow: mature cells - CD45+CD34-CD19+CD22+. B) sIgM/CD34/CD19/CD10 combination - black: immature cells - sIgM-CD34+CD19+CD10-/+ red: intermediate cells - sIgM+CD34-/+CD19+CD10-/+ yellow: mature cells - sIgM+CD34-CD19+CD10-/+.

Eliane Borges-Almeida, et al. BMC Infect Dis. 2011;11:38-38.
2.
Figure 2

Figure 2. From: The impact of maternal HIV infection on cord blood lymphocyte subsets and cytokine profile in exposed non-infected newborns.

Analysis of T cell proliferation of non-stimulated (A) and PHA-stimulated (B) cord mononuclear cells of a newborn from a HIV-infected mother. After gating of CD3 cells, events were analyzed for size and complexity (forward-scatter and side-scatter gates), from which resting (R1-green) and blast cells (R2-blue) were separated. T-lymphocyte subsets were then analyzed. Dead cells (red) were excluded from all analyses. T cell proliferation was the difference between the percentages of PHA-stimulated blasts and non-stimulated blasts.

Eliane Borges-Almeida, et al. BMC Infect Dis. 2011;11:38-38.

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