Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
3374974 | Journal of Infection | 2012 | 7 Pages |
SummaryObjectivesAnalyze the short-term immunological effect directly attributable to MRV without interference of other drugs.MethodsMRV group included experienced HIV-infected patients undergoing an 8-day MRV monotherapy. A comparison population included naïve HIV-infected patients starting combined antiretroviral therapy (cART group). Absolute CD4+ and CD8+ T-cells and T-lymphocyte subsets were determined at day 0 and 8.ResultsFifty-nine patients who underwent MRV monotherapy and 28 naïve patients were analyzed. Forty-one patients in the MRV group experienced a significant viral load decrease (MRV positive subgroup). Virological response and CD4+ T-cell change were comparable in the MRV positive and cART groups. CD8+ T-cell increase in the MRV positive subgroup showed a trend toward superiority when compared with the cART group. T-lymphocyte subset changes showed a similar profile in the MRV positive and cART groups with a differential effect in the TemRA cells related to MRV. No immunological effect (absolute lymphocyte counts or subsets) was observed in patients without virological response to MRV.ConclusionsMRV produced CD4+ and CD8+ T-cell gains related to antiviral activity and comparable or even superior in terms of CD8+ T-cells to naïve patients starting cART. No immunological effect occurred in subjects without virological response to MRV.