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Cartography of Virologic Reservoir Related to Antiretroviral Concentrations in HIV-1 Chronic Patients Treated by a First Line Treatment Containing Dolutegravir and Associated Nucleoside / Nucleotide Reverse Transcriptase Inhibitors Backbone

A Prospective Study Aiming to Determine the Cartography of Virological Reservoir Related to Antiretroviral Concentrations in Chronic HIV-1 Patients Treated With a First Line of Dolutegravir and Associated Nucleoside / Nucleotide Reverse Transcriptase Inhibitors (NRTIs).

Status
Completed
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04133012
Acronym
DOLUVOIR
Enrollment
20
Registered
2019-10-21
Start date
2020-02-10
Completion date
2023-06-09
Last updated
2026-04-13

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

HIV-1 Infection

Keywords

Viral cartography, Viral reservoir, Antiretroviral treatments diffusion

Brief summary

The main objective of the study is to characterize the diffusion of dolutegravir and associated backbone (abacavir/lamivudine or tenofovir/emtricitabine) in HIV-1 chronic patients in the main putative reservoirs, namely inguinal lymph nodes, rectal, fat tissues and sperm.

Detailed description

The major obstacle to a functional cure of HIV infection is the persistence of the latent HIV reservoir. Several arguments suggest the persistence of a residual viral replication in different compartments, despite an effective antiretroviral treatment. This residual viral replication partially comes from pharmacological sanctuaries where the drugs do not largely penetrate. In such sanctuaries a recent report published in Nature has shown that the virus can replicate with less antiviral pressure contributing to continuously replenish the reservoirs. Nevertheless, this study concerned a limited number of patients and only blood and lymph-node samples were collected for viral analysis. Moreover, the drug distribution was estimated based on mathematical hypotheses without drug measure concentration. The International AIDS Society recommend for most patients an optimal initial regimen containing 2 nucleoside reverse transcriptase inhibitors (NRTIs) plus an integrase strand transfer inhibitor (InSTI)2. The new integrase inhibitor dolutegravir is more and more widely used in combination with nucleoside/nucleotide reverse transcriptase. Indeed, this drug shows a good tolerance and demonstrates a particularly fast inhibition of the viral replication. Moreover, dolutegravir is active against HIV strains that are resistant to the first generation of integrase inhibitors, raltegravir and elvitegravir. However the penetration of dolutegravir in deep compartments has not been fully characterized: the studies comprised a small number of patients and were not able to estimate the distribution in several compartments at the same time for each patient. Moreover the levels of residual viral replication in those compartments during treatment are unknown, making it difficult to evaluate the capacity of this drug and associated backbone to efficiently act against viral reservoirs maintenance. The aim of the study is to measure simultaneously dolutegravir and nucleoside/nucleotide reverse transcriptase inhibitors in different compartments to obtain cartography of dolutegravir and associated backbone distribution and the spatial dynamics of virus in each patient. The decision to study dolutegravir and the two associated backbones (abacavir / lamivudine or tenofovir /emtricitabine) was decided as: * The International AIDS Society recommend for most patients an optimal initial regimen containing 2 nucleoside reverse transcriptase inhibitors (NRTIs) plus an integrase strand transfer inhibitor (InSTI)2. * Dolutegravir viral power is established for high levels of viral load 90 and this drug is widely used. * This study is very complementary of studies ANRS SIVART and ANRS 169 OPTIPRIM 2. * Dolutegravir is combined with abacavir + lamivudine in a single-tablet and is largely prescribed. * Raltegravir and elvitegravir will not be analysed because the number of recruited patients should be more important to obtain sufficient data and the feasibility would not be sure.

Interventions

OTHERSamplings

* blood samples * rectal biopsies * nodes biopsies * cutaneous fat tissues biopsies * semen sample

Sponsors

ANRS, Emerging Infectious Diseases
Lead SponsorOTHER_GOV
ViiV Healthcare
CollaboratorINDUSTRY

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
BASIC_SCIENCE
Masking
NONE

Eligibility

Sex/Gender
MALE
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Male HIV-1 infected subjects * Age \> or = 18 years old * Currently receiving as first line therapy 7 days a week for at least 18 months with dolutegravir (at 50 mg once a day) and two nucleoside/nucleotide reverse transcriptase inhibitors (abacavir/lamivudine or ,tenofovir/emtricitabine) or * Receiving first-line therapy 7 days a week for at least 18 months with dolutegravir (50 mg once daily) + abacavir/lamivudine followed by dual therapy with dolutegravir + lamivudine for at least 6 months; or * Receiving first-line therapy 7 days a week for at least 18 months with dolutegravir + tenofovir / emtricitabine followed by dual therapy with dolutegravir + lamivudine for at least 6 months. * HIV RNA currently \<50 Cp/mL, , and \<50 Cp/mL 6 months after treatment initiation and \<50 Cp/mL confirmed at 12 months after treatment initiation * Normal PT, APTT and platelet count values at screening * Written and informed consent signed by the person and the investigator (no later than the day of pre-enrollment and prior to any examination carried out as part of the study (article L1122-1-1 of the Public Health Code) * Person affiliated or beneficiary of a social security scheme (article L1121-11 of the Public Health Code) (State Medical Aid or AME is not a social security scheme)

Exclusion criteria

* Single HIV-2 infection * Dolutegravir antiretroviral monotherapy * Contraindication to biopsy, taking anticoagulant and antiplatelet drugs * Hemophilia * Symptomatic sexually transmitted infection * Being under guardianship or trusteeship mandate for future protection * Participation in another research involving the human person, of category 1 or 2, * Associated treatments (Carbamazepine, Oxcarbazepine, Phenytoin, Phenobarbital, Rifampicin, St. John's Wort)

Design outcomes

Primary

MeasureTime frameDescription
Characterization of the diffusion of dolutegravir and associated backbone (abacavir/lamivudine or tenofovir/emtricitabine) in spermAt Day 0, At time T0 (before taking treatments)Dosage of the different antiretroviral drugs molecules in sperm
Characterization of the diffusion of dolutegravir and associated backbone (abacavir/lamivudine or tenofovir/emtricitabine) in lymph nodesAt Day 0, between T1 (maximum 3 hours after tacking treatments) and T3 (8 hours after taking treatments)Dosage of the different antiretroviral drugs molecules in lymph nodes
Characterization of the diffusion of dolutegravir and associated backbone (abacavir/lamivudine or tenofovir/emtricitabine) in fat tissuesAt Day 0, between T1 (maximum 3 hours after tacking treatments) and T3 (8 hours after taking treatments)Dosage of the different antiretroviral drugs molecules in fat tissues
Characterization of the diffusion of dolutegravir and associated backbone (abacavir/lamivudine or tenofovir/emtricitabine) in rectal tissuesAt Day 0, T1 (maximum 3 hours after taking treatment)Dosage of the different antiretroviral drugs molecules in rectal tissues

Secondary

MeasureTime frameDescription
Characterization of the level of the replication (RNA-HIV) and the level of infection (DNA-HIV) in the reservoirsAt Day 0Analyze and comparison of the level of viral transcription by measuring the cell-associated HIV- RNA in the different tissues and fluids: lymphoid, rectal, genital secretion, blood and fat biopsies as well as cerebrospinal fluid. Analyze and comparison of the reservoir level by measuring the cell-associated total HIV- DNA in the different tissues and fluids
Study of the spatial dynamics of viral quasi-species In the different reservoirsAt Day 0Analyze of the spatial dynamics of HIV-DNA and HIV-RNA from Lymphoid, rectal, genital secretion, blood, fat cells by phylogenetic analyses after sequencing Env HIV-DNA and HIV-RNA
Study of the mutations of resistance in the integrase geneAt Day 0Description of resistance mutations in Integrase gene which could be linked to suboptimal concentrations of dolutegravir
Description for each compartment of the relationship between exposure to therapeutic combinations and the level of infection / viral replicationAt Day 0Characterization of the relationship between the concentration of dolutegravir and backbone drugs with the level of wild type viral replication in the different compartments. Analyze of the impact of backbone drugs associated to dolutegravir on viral level production. Correlation between the level of resistant virus replication and the exposure to dolutegravir and the backbone drugs. Evaluation by simulation the effect of different dosing regimen of dolutegravir (including higher doses) on the level of viral replication and on resistance

Countries

France

Contacts

PRINCIPAL_INVESTIGATORAntoine CHERET

CHU Pointe-à-Pitre/Abymes

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Apr 14, 2026