Treatment Intensification Followed By Interleukin-7 Reactivates Hiv Without Reducing Total Hiv Dna: A Randomized Trial

Background:As a first step towards HIV cure, we assessed a strategy of antiretroviral therapy (ART) intensification followed by interleukin-7 (IL-7) used as an HIV-reactivating agent.Methods:A multicentre, randomized clinical trial included patients on suppressive ART with CD4(+) cell counts at least 350/l and HIV-DNA between 10 and 1000copies/10(6) peripheral blood mononuclear cells (PBMCs). After an 8-week raltegravir and maraviroc intensification, patients were randomized to intensification alone or with 3 weekly IL-7 injections at weeks 8, 9 and 10. The primary endpoint was at least 0.5 log(10) decrease in HIV-DNA in PBMC at W56. Secondary endpoints included ultrasensitive plasma viremia, immunologic changes and safety.Results:Twenty-nine patients were enrolled with median baseline 558 CD4(+) cell counts/l, 360 HIV-DNA copies/10(6) PBMCs and 12 years on ART. No patient in either arm achieved the primary endpoint. Addition of IL-7 induced a significant expansion of CD4(+) T cells, primarily central-memory cells (+5%, P=0.001) at week 12, together with an increase in levels of HIV-DNA/10(6) PBMC (+0.28 log(10)copies/P=0.001), and the proportion of patients with detectable ultrasensitive plasma HIV-RNA increased compared with week 8 (P=0.07). At weeks 56 and 80, total and memory CD4(+) cell counts and total HIV-DNA/ml of blood remained elevated. In contrast, HIV-DNA/million PBMC and plasma viremia returned to baseline levels whereas activated HLA-DR(+)CD4(+) T cells significantly decreased.Conclusion:IL-7 administration and dual ART intensification induced, despite a mild HIV reactivation, an amplification of the HIV reservoir, as a result of central-memory CD4(+) T-cell expansion, thus limiting this IL-7 based strategy.Clinical trial registration:This trial was registered with ClinicalTrials.gov, number NCT01019551.