%0 Journal Article %1 ibanez1999quantification %A Ibáñez, Angela %A Puig, Teresa %A Elias, Johannes %A Clotet, Bonaventura %A Ruiz, Lydia %A Martínez, Miguel Angel %D 1999 %J AIDS (London, England) %K Anti-{HIV}_Agents Combination Drug_Therapy Gutachtersystem Habilitation Humans Indinavir Proviruses Reverse_Transcriptase_Inhibitors Ritonavir Viral Viral_Load je {CD4}_Lymphocyte_Count {DNA} {HIV-1} {HIV}_Infections {HIV}_Protease_Inhibitors {RNA} %N 9 %P 1045--9 %R 10397534 %T Quantification of integrated and total HIV-1 DNA after long-term highly active antiretroviral therapy in HIV-1-infected patients %V 13 %X OBJECTIVE: To assess the impact of long-term virus suppression on the peripheral blood CD4 T cells integrated and total HIV-1 DNA loads in patients receiving highly active antiretroviral therapy (HAART). METHODS: A total of 10 HIV-1-infected patients receiving a triple combination therapy (two nucleoside analogues and one protease inhibitor) were longitudinally studied to compare integrated and total HIV-1 DNA loads. HIV-1 DNA quantification was performed using a quantitative nested polymerase chain reaction (PCR) on genomic peripheral blood mononuclear cell (PBMC) DNA obtained at baseline and at 48 weeks of HAART. RESULTS: All the study patients showed an early and sustained decrease in plasma HIV-1 RNA to below the limit of detection (200 copies/ml). Concordant with the plasma viral decline, a significant increase in the CD4 T cell count was observed (P = 0.007). A statistically significant fivefold decrease in total HIV-1 DNA was detected after 48 weeks of HAART (P = 0.005). However, no statistically significant change was noted after the therapy when the integrated HIV-1 DNA copy number was compared (P = 0.333). Taken together, these results suggest that in the patients analysed the integrated HIV-1 DNA does not decay rapidly after HAART. CONCLUSION: Within the study cohort the total amount of PBMC HIV-1 DNA decreased drastically after 48 weeks of HAART. Nevertheless, the integrated HIV-1 DNA did not significantly decay during this period. Although the data presented here are limited by the number of patients analysed, our findings suggest that 48 weeks of HAART does not significantly reduce the integrated HIV-1 proviral DNA load in the latently infected CD4 T cell reservoir.

@article{ibanez1999quantification, abstract = {{OBJECTIVE:} To assess the impact of long-term virus suppression on the peripheral blood {CD4} T cells integrated and total {HIV-1} {DNA} loads in patients receiving highly active antiretroviral therapy ({HAART).} {METHODS:} A total of 10 {HIV-1-infected} patients receiving a triple combination therapy (two nucleoside analogues and one protease inhibitor) were longitudinally studied to compare integrated and total {HIV-1} {DNA} loads. {HIV-1} {DNA} quantification was performed using a quantitative nested polymerase chain reaction ({PCR)} on genomic peripheral blood mononuclear cell ({PBMC)} {DNA} obtained at baseline and at 48 weeks of {HAART.} {RESULTS:} All the study patients showed an early and sustained decrease in plasma {HIV-1} {RNA} to below the limit of detection (200 copies/ml). Concordant with the plasma viral decline, a significant increase in the {CD4} T cell count was observed (P = 0.007). A statistically significant fivefold decrease in total {HIV-1} {DNA} was detected after 48 weeks of {HAART} (P = 0.005). However, no statistically significant change was noted after the therapy when the integrated {HIV-1} {DNA} copy number was compared (P = 0.333). Taken together, these results suggest that in the patients analysed the integrated {HIV-1} {DNA} does not decay rapidly after {HAART.} {CONCLUSION:} Within the study cohort the total amount of {PBMC} {HIV-1} {DNA} decreased drastically after 48 weeks of {HAART.} Nevertheless, the integrated {HIV-1} {DNA} did not significantly decay during this period. Although the data presented here are limited by the number of patients analysed, our findings suggest that 48 weeks of {HAART} does not significantly reduce the integrated {HIV-1} proviral {DNA} load in the latently infected {CD4} T cell reservoir.}, added-at = {2014-02-06T19:13:55.000+0100}, author = {Ibáñez, Angela and Puig, Teresa and Elias, Johannes and Clotet, Bonaventura and Ruiz, Lydia and Martínez, Miguel Angel}, biburl = {https://www.bibsonomy.org/bibtex/2e89345940e82468cf8648303669e5dd2/ag_vogel}, doi = {10397534}, interhash = {4726e8b1b4159f4977b735ac14b0b26f}, intrahash = {e89345940e82468cf8648303669e5dd2}, issn = {0269-9370}, journal = {{AIDS} (London, England)}, keywords = {Anti-{HIV}_Agents Combination Drug_Therapy Gutachtersystem Habilitation Humans Indinavir Proviruses Reverse_Transcriptase_Inhibitors Ritonavir Viral Viral_Load je {CD4}_Lymphocyte_Count {DNA} {HIV-1} {HIV}_Infections {HIV}_Protease_Inhibitors {RNA}}, month = jun, note = {{PMID:} 10397534}, number = 9, pages = {1045--9}, timestamp = {2014-02-06T19:14:04.000+0100}, title = {Quantification of integrated and total {HIV-1} {DNA} after long-term highly active antiretroviral therapy in {HIV-1-infected} patients}, volume = 13, year = 1999 }