Background
It was recently hypothesized that the lentiviral reservoir in central memory (TCM) and transitional memory (TTM) CD4+ cells could be restricted by new therapies targeting pathways downstream of homeostatic proliferation or pathways associated with “stem cell–ness”, such as those developed for the treatment of leukemias. Gar1041 is one such epigenetic drug adopted in the experimental treatment of certain types of leukemia.
Methods
SIVmac251-infected primates with viral loads stably suppressed by ART (tenofovir/emtricitabine/raltegravir) were administered for two months: Gar1041 twice daily (a starting dose of 1.5g in the first week followed by 2g in the remaining period). ART was continued during Gar1041 treatment. Proviral DNA was quantitated using a Taqman real-time PCR.
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Results
The proviral DNA content of PBMCs, which had shown no significant changes during 54 days of treatment with ART alone (p >0.05), fell below the level of detection (2 copies/106 cells) in all study subjects within one month of Gar1041 treatment (p <0.05; Bonferroni’s test following significant [p=0.0003] repeated measures ANOVA). No significant changes were noticed in a control group treated with ART alone (p=0.49). The decrease in proviral DNA was associated with a significant (p=0.0156) decrease in the proportions of the TCM CD4+ cell subpopulation in peripheral blood. However, both proviral DNA and the proportions of TCM CD4+ rebound after two months of therapy.
Conclusions
The present study furnishes proof of concept that pharmacological strategies may impact on the proviral DNA reservoir. However, the renewal of the phenotype TCM compartment, associated with the reconstitution of proviral DNA in peripheral blood from an as yet unidentified reservoir, will require integration with other experimental approaches.
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