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. Author manuscript; available in PMC: 2008 Oct 31.
Published in final edited form as: J Immunol Methods. 2007 Aug 8;327(1-2):75–81. doi: 10.1016/j.jim.2007.07.017

Figure 3. Level of viral production and calculated levels of viral inhibition measured by the autologous T cell co-culture method in the absence of NL4-3 superinfection.

Figure 3

PBMC were isolated from blood from HIV+ donors and stimulated with bi-specific antibodies to produce pure CD4+ and CD8+ T lymphocyte cultures. After 14 days the CD8+ T lymphocytes were added to the wells containing autologous CD4+ cells at three different ratios (0.5:1, 1:1, and 2:1), each in triplicate. Media only was added to three wells as a positive control for maximum viral production in the absence of CD8+ T lymphocytes. Viral production was measured by p24 ELISA at three time points, as described in Materials and Methods. Panel a shows the actual p24 production at three different time-points from HIV+ Donor 1 and Panel b shows the calculated percent inhibition using the formula described in the Figure 2 legend.