Figure 4
Figure 4. Inhibition of HIV-1 trans-infection by various HIV-1–specific Abs. HIV-1–specific Abs were added 2 hours after the infection of immature MoDCs at the same time as PHA-activated CD4 T lymphocytes. After 48 hours of culture, infection was determined by the detection of HIV-1 intracellular p24 Ag production by flow cytometry or by the detection of viral p24 Ag released into the supernatant by ELISA. Percentages of infected MoDCs (black squares) or CD4 T lymphocytes (gray triangles) after coculture in the presence of a panel of different anti–HIV-1–specific Abs: anti-gp120 NAbs b12 (A) and 2G12 (B); anti-gp41 NAbs 4E10 (C) and 2F5 (D); and NNAbs 246-D (E) and 4B3 (F). The percentage of viral p24 released into the supernatant of the coculture is indicated by black dots and asterisks. Dashed lines correspond to the IC70 concentrations of Abs. The curve corresponds to the means ± SD of at least 4 independent experiments performed with cells from 4 different healthy blood donors.

Inhibition of HIV-1 trans-infection by various HIV-1–specific Abs. HIV-1–specific Abs were added 2 hours after the infection of immature MoDCs at the same time as PHA-activated CD4 T lymphocytes. After 48 hours of culture, infection was determined by the detection of HIV-1 intracellular p24 Ag production by flow cytometry or by the detection of viral p24 Ag released into the supernatant by ELISA. Percentages of infected MoDCs (black squares) or CD4 T lymphocytes (gray triangles) after coculture in the presence of a panel of different anti–HIV-1–specific Abs: anti-gp120 NAbs b12 (A) and 2G12 (B); anti-gp41 NAbs 4E10 (C) and 2F5 (D); and NNAbs 246-D (E) and 4B3 (F). The percentage of viral p24 released into the supernatant of the coculture is indicated by black dots and asterisks. Dashed lines correspond to the IC70 concentrations of Abs. The curve corresponds to the means ± SD of at least 4 independent experiments performed with cells from 4 different healthy blood donors.

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