Strong in vitro synergy between the fusion inhibitor T-20 and the CXCR4 blocker AMD-3100

Attachment and entry of HIV-1 into CD4 cells involve a series of events in which different viral envelope proteins interact with specific cell recepto rs, culminating in fusion of viral and cell membranes. AMD-3100 is a small molecule inhibitor of HIV-1 attachment to the CXCR4 chemokine receptor, and T-20 is a synthetic peptide corresponding to a region of HIV-1 gp41 that b locks fusion to cell membranes. To evaluate the interaction between agents acting at two different steps of the entry process, we conducted in vitro s tudies of the combination of T-20 and AMD-3100 against an X4 HIV-1 isolate. Single drugs or multiply diluted fixed ratio combinations of drugs were ad ded to peripheral blood mononuclear cells infected with a clinical isolate, 14aPre. Drug interactions were evaluated using the median-effect principle and the combination index technique. The 50% inhibitory concentration (IC5 0) for T-20 was 0.10 mug/ml and for AMD-3100 was 0.19 mug/ml. Synergy was o bserved between T-20 and AMD-3100 and this increased with higher inhibitory concentrations, with combination indices ranging from 0.62 at IC50 to 0.02 at IC95. Whether these synergistic interactions translate into clinical be nefit will need to be addressed in the context of clinical trials.