Fig. 1.
Fig. 1. Inhibition of HIV-1BZ167 replication by alloantigen-stimulated cell lines. (A) PHA blasts were infected with 859 TCID50/105 cells, as described in Materials and Methods section. Infected PHA blasts were cultured in the absence (□) or presence of an alloantigen-stimulated cell line derived from the same cells donor as the PHA blasts (autologous, •) or an alloantigen-stimulated cell line derived from an unrelated donor (heterologous, ▴). HIV-1 p24 core antigen was determined by ELISA. The results represent means of triplicate cultures. (B) HIV-1BZ167–infected PHA blasts (172 TCID50/105 cells) were incubated in the absence or presence of an alloantigen-stimulated cell line before and after depletion of CD4+ T cells, using anti-CD4–coated magnetic beads. Results are expressed as p24 antigen production from one experiment determined by ELISA.

Inhibition of HIV-1BZ167 replication by alloantigen-stimulated cell lines. (A) PHA blasts were infected with 859 TCID50/105 cells, as described in Materials and Methods section. Infected PHA blasts were cultured in the absence (□) or presence of an alloantigen-stimulated cell line derived from the same cells donor as the PHA blasts (autologous, •) or an alloantigen-stimulated cell line derived from an unrelated donor (heterologous, ▴). HIV-1 p24 core antigen was determined by ELISA. The results represent means of triplicate cultures. (B) HIV-1BZ167–infected PHA blasts (172 TCID50/105 cells) were incubated in the absence or presence of an alloantigen-stimulated cell line before and after depletion of CD4+ T cells, using anti-CD4–coated magnetic beads. Results are expressed as p24 antigen production from one experiment determined by ELISA.

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