» Articles » PMID: 25153969

A Very Low Geno2pheno False Positive Rate is Associated with Poor Viro-immunological Response in Drug-naïve Patients Starting a First-line HAART

Abstract

Background: We previously found that a very low geno2pheno false positive rate (FPR ≤ 2%) defines a viral population associated with low CD4 cell count and the highest amount of X4-quasispecies. In this study, we aimed at evaluating whether FPR ≤ 2% might impact on the viro-immunological response in HIV-1 infected patients starting a first-line HAART.

Methods: The analysis was performed on 305 HIV-1 B subtype infected drug-naïve patients who started their first-line HAART. Baseline FPR (%) values were stratified according to the following ranges: ≤ 2; 2-5; 5-10; 10-20; 20-60; >60. The impact of genotypically-inferred tropism on the time to achieve immunological reconstitution (a CD4 cell count gain from HAART initiation ≥ 150 cells/mm(3)) and on the time to achieve virological success (the first HIV-RNA measurement <50 copies/mL from HAART initiation) was evaluated by survival analyses.

Results: Overall, at therapy start, 27% of patients had FPR ≤ 10 (6%, FPR ≤ 2; 7%, FPR 2-5; 14%, FPR 5-10). By 12 months of therapy the rate of immunological reconstitution was overall 75.5%, and it was significantly lower for FPR ≤ 2 (54.1%) in comparison to other FPR ranks (78.8%, FPR 2-5; 77.5%, FPR 5-10; 71.7%, FPR 10-20; 81.8%, FPR 20-60; 75.1%, FPR >60; p = 0.008). The overall proportion of patients achieving virological success was 95.5% by 12 months of therapy. Multivariable Cox analyses showed that patients having pre-HAART FPR ≤ 2% had a significant lower relative adjusted hazard [95% C.I.] both to achieve immunological reconstitution (0.37 [0.20-0.71], p = 0.003) and to achieve virological success (0.50 [0.26-0.94], p = 0.031) than those with pre-HAART FPR >60%.

Conclusions: Beyond the genotypically-inferred tropism determination, FPR ≤ 2% predicts both a poor immunological reconstitution and a lower virological response in drug-naïve patients who started their first-line therapy. This parameter could be useful to identify patients potentially with less chance of achieving adequate immunological reconstitution and virological undetectability.

Citing Articles

Role of pretreatment variables on plasma HIV RNA value at the sixth month of antiretroviral therapy including all first line drugs in HIV naïve patients: A path analysis approach.

Mengoli C, Basso M, Andreis S, Scaggiante R, Cruciani M, Ferretto R PLoS One. 2019; 14(3):e0213160.

PMID: 30856186 PMC: 6411145. DOI: 10.1371/journal.pone.0213160.


Switch to maraviroc with darunavir/r, both QD, in patients with suppressed HIV-1 was well tolerated but virologically inferior to standard antiretroviral therapy: 48-week results of a randomized trial.

Rossetti B, Gagliardini R, Meini G, Sterrantino G, Colangeli V, Re M PLoS One. 2017; 12(11):e0187393.

PMID: 29161288 PMC: 5697828. DOI: 10.1371/journal.pone.0187393.


Monophylogenetic HIV-1C epidemic in Ethiopia is dominated by CCR5-tropic viruses-an analysis of a prospective country-wide cohort.

Kalu A, Telele N, Gebreselasie S, Fekade D, Abdurahman S, Marrone G BMC Infect Dis. 2017; 17(1):37.

PMID: 28061826 PMC: 5219668. DOI: 10.1186/s12879-016-2163-1.


Impact of HIV-1 tropism on the emergence of non-AIDS events in HIV-infected patients receiving fully suppressive antiretroviral therapy.

Maffongelli G, Alteri C, Gentilotti E, Bertoli A, Ricciardi A, Malagnino V AIDS. 2015; 30(5):731-41.

PMID: 26595543 PMC: 4937812. DOI: 10.1097/QAD.0000000000000977.

References
1.
Feinberg M, McCune J, Miedema F, Moore J, Schuitemaker H . HIV tropism and CD4+ T-cell depletion. Nat Med. 2002; 8(6):537. DOI: 10.1038/nm0602-537a. View

2.
Carrillo A, Ratner L . Human immunodeficiency virus type 1 tropism for T-lymphoid cell lines: role of the V3 loop and C4 envelope determinants. J Virol. 1996; 70(2):1301-9. PMC: 189948. DOI: 10.1128/JVI.70.2.1301-1309.1996. View

3.
Moore R, Gebo K, Lucas G, Keruly J . Rate of comorbidities not related to HIV infection or AIDS among HIV-infected patients, by CD4 cell count and HAART use status. Clin Infect Dis. 2008; 47(8):1102-4. PMC: 2597666. DOI: 10.1086/592115. View

4.
Coakley E, Reeves J, Huang W, Mangas-Ruiz M, Maurer I, Harskamp A . Comparison of human immunodeficiency virus type 1 tropism profiles in clinical samples by the Trofile and MT-2 assays. Antimicrob Agents Chemother. 2009; 53(11):4686-93. PMC: 2772338. DOI: 10.1128/AAC.00229-09. View

5.
Alteri C, Svicher V, Gori C, DArrigo R, Ciccozzi M, Ceccherini-Silberstein F . Characterization of the patterns of drug-resistance mutations in newly diagnosed HIV-1 infected patients naïve to the antiretroviral drugs. BMC Infect Dis. 2009; 9:111. PMC: 2725045. DOI: 10.1186/1471-2334-9-111. View