HIV Infections
Conditions
Keywords
HIV, persistence, reservoirs, residual replication, gut, gut-associated lymphoid tissue, treatment experienced
Brief summary
The PLUS study is a pilot study to measure the effect of therapy intensification (with raltegravir and optional second agent) on HIV levels in the gut and blood in patients on antiretroviral therapy (ART) with viral load \< 50 copies/mL (herein referred to as suppressed). We hypothesize that there is ongoing replication in the gut despite suppressive ART and that this replication can be inhibited by the addition of one or two new antiretroviral drugs whose activity affects a distinct part of the viral life cycle. All study participants will have upper and lower endoscopy at baseline (before intensification) and after intensification. These endoscopies will be used to obtain gut tissue and single cells (for CD4+ cells) .
Detailed description
The PLUS study is a prospective, longitudinal pilot study to measure the effect of therapy intensification (with raltegravir and possible addition of a study PI or NNRTI-Non-Nucleoside Reverse Transcriptase Inhibitor) on HIV-1 DNA/RNA levels in the gut-associated lymphoid tissue (GALT) and blood in patients on ART with viral load (VL) \< 50 copies/mL (herein referred to as suppressed). We hypothesize that there is ongoing replication in the GALT despite suppressive ART and that this replication can be inhibited by the addition of one or two new antiretroviral drugs whose activity affects a distinct part of the viral life cycle. All study participants will have a colonoscopy and esophagogastroduodenoscopy (EGD) at baseline (before intensification) and a second colonoscopy with EGD 12 weeks after intensification. These endoscopies will be used to obtain GALT mononuclear cells (for CD4+ lymphocytes) as well as tissue for in situ hybridization and immunohistochemical studies.
Interventions
DRUGraltegravir
The baseline ART regimen will be intensified with raltegravir 400mg orally (PO) twice daily (BID) (all participants) +/- a study NNRTI or protease inhibitor (PI) (at the option of the participant and the study clinical team).
DRUGStudy NNRTI
Subjects who are not already on an NNRTI and who are suitable candidates will have the option of adding a study NNRTI (either efavirenz or etravirine).
DRUGStudy PI
Subjects who are not on a PI and who are suitable candidates will have the option of adding a study PI. PIs used as study drugs will include atazanavir (+/- ritonavir), fosamprenavir (+/-ritonavir), lopinavir/ritonavir, and darunavir/ritonavir.
Sponsors
University of California, San Francisco
Study design
Allocation
NA
Intervention model
SINGLE_GROUP
Masking
NONE
Eligibility
Sex/Gender
ALL
Age
18 Years to 65 Years
Healthy volunteers
No
Inclusion criteria
1. Age 18 to 65 years 2. Infection with HIV-1, as documented by a licensed ELISA and confirmed by a Western blot or HIV-1 RNA at any time prior to study entry 3. On ART for at least 12 months prior to study entry with a regimen that includes at least two NRTIs and either an NNRTI or PI 4. No change in ART for at least 3 months prior to study entry. 5. CD4+ T cell count of 200 or greater within 30 days prior to study entry. 6. HIV-1 RNA level consistently below the limit of detection of commercial ultrasensitive assays (\<50 copies/mL) for at least 6 months before study entry. 7. Women of reproductive potential (those who have not undergone surgical sterilization via hysterectomy, bilateral oophorectomy, or tubal ligation and who have had menses in the preceding 24 months) must have a negative urine or serum pregnancy test within 48 hours prior to study entry. 8. All subjects must agree not to participate in the process of conception (such as active attempts to impregnate or become pregnant, sperm or egg donation, in vitro fertilization) while receiving study drugs and for 6 weeks after stopping study drugs. If participating in sexual activity that could lead to pregnancy, the subject and/or partner should use at least two reliable methods of contraception, including oral contraceptive pills, an intrauterine device (IUD), condoms, and a diaphragm or cervical cap with spermicide. 9. Ability and willingness to provide informed consent.
Exclusion criteria
1. Any condition that, in the opinion of the GI specialist, would either be a contraindication to endoscopy or would increase the risk from sedation, endoscopy, or mucosal biopsies. These conditions may include, but are not limited to: * Significant complication (such as perforation) from prior endoscopy * Known bleeding diathesis * Platelet count \< 100,000 per microliter * INR \> 1.6 * Current use of antiplatelet agents (aspirin, other NSAIDS, clopidogrel (Plavix), other antiplatelet agents) or anticoagulants (heparin, low molecular weight heparin, warfarin, lepirudin, or other anticoagulants) and inability to temporarily hold such medications for endoscopy. * Active angina, unstable angina, or MI within 2 months prior to study entry * Decompensated CHF * Respiratory insufficiency with FEV1 \< 1L, resting hemoglobin saturation of \<92%, or need for oxygen supplementation * OSA requiring CPAP * Ongoing substance abuse * Peripheral glucose \> 350 mg/dL 2. Prior use of raltegravir 3. Any condition that, in the opinion of the infectious disease (ID) specialist, would be a contraindication to raltegravir. These conditions may include, but are not limited to: unstable clinical condition (such as recent hospitalization, cancer with need for chemotherapy or radiation); severe hepatic insufficiency; need for contraindicated medicines; breastfeeding; or high risk for myopathy or rhabdomyolysis. 4. Calculated creatinine clearance (CrCl) \< 50 mL/min, as estimated by the Cockcroft-Gault equation 5. AST (SGOT), ALT (SGPT), alkaline phosphatase, or bilirubin \> 3x the upper limit of normal (ULN). 6. LDL \> 200 mg/dL or TG \> 400 mg/dL in fasting lipids, as measured within three months prior to screening or at the time of screening 7. Plan to change the background ART within 16 weeks after study entry 8. Receipt of any HIV vaccine 9. Receipt of a non-HIV vaccine within 30 days prior to study entry 10. An opportunistic infection within 60 days prior to study entry 11. Use of significant immunosuppressive medications (such as systemic corticosteroids, tacrolimus, sirolimus, mycophenolate, azathioprine, interferon, and cancer chemotherapy) within 60 days prior to study entry. 12. Active drug or alcohol abuse that, in the opinion of the investigator, would interfere with adherence to the requirements of the study
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Number of Subjects Who Had a Decrease in HIV RNA Per Million CD4+ T Cells in the Ileum | 12 weeks | Number of subjects who had a decrease from week 0 to week 12 in unspliced cell-associated HIV RNA per million CD4+ T cells in the ileum |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| Number of Subjects Who Experienced an Increase in CD4+ T Cells (as a % of All Cells) in the Ileum. | 12 weeks | Number of subjects who experienced an increase in CD4+ T cells (as a % of all cells) in the ileum (by flow cytometry) from week 0 to week 12. |
| Number of Subjects Who Experienced an Increase in CD4% in the Ileum. | 12 weeks | Number of subjects who experienced an increase from week 0 to week 12 in CD4+ T cells (as a % of T cells, by flow cytometry) in the ileum |
| Average Change in Activated (CD38+HLADR+) CD8+ T Cells in the Ileum | 12 weeks | Average of changes(week 0-week 12) in the % of CD8+ T cells that are CD38+HLA-DR+, by flow cytometry |
Countries
United States
Participant flow
Participants by arm
| Arm | Count |
|---|---|
| Intensification Arm In addition to continuing the baseline ART regimen (2 NRTIs and either a PI or NNRTI), all subjects will receive raltegravir 400mg PO (by mouth) BID (twice daily). Subjects who are suitable candidates will have the option of adding a second drug, consisting of either a study NNRTI or a study PI. Subjects who are not already on an NNRTI and who are suitable candidates will have the option of adding a study NNRTI (either efavirenz or etravirine), while subjects who are not on a PI and who are suitable candidates will have the option of adding a study PI. PIs used as study drugs will include atazanavir (+/- ritonavir), fosamprenavir (+/-ritonavir), lopinavir/ritonavir, and darunavir/ritonavir. | 8 |
| Total | 8 |
Withdrawals & dropouts
| Period | Reason | FG000 |
|---|---|---|
| Overall Study | Withdrawal by Subject | 1 |
Baseline characteristics
| Characteristic | Intensification Arm |
|---|---|
| Age, Categorical <=18 years | 0 Participants |
| Age, Categorical >=65 years | 0 Participants |
| Age, Categorical Between 18 and 65 years | 8 Participants |
| Age Continuous | 48.9 years STANDARD_DEVIATION 11.5 |
| Region of Enrollment United States | 8 participants |
| Sex: Female, Male Female | 0 Participants |
| Sex: Female, Male Male | 8 Participants |
Adverse events
| Event type | EG000 affected / at risk |
|---|---|
| deaths Total, all-cause mortality | — / — |
| other Total, other adverse events | 0 / 8 |
| serious Total, serious adverse events | 0 / 8 |
Outcome results
Primary
Number of Subjects Who Had a Decrease in HIV RNA Per Million CD4+ T Cells in the Ileum
Number of subjects who had a decrease from week 0 to week 12 in unspliced cell-associated HIV RNA per million CD4+ T cells in the ileum
Time frame: 12 weeks
Population: We analyzed data from all subjects who had endosocopies at week 12.
| Arm | Measure | Value (NUMBER) |
|---|---|---|
| Intensification Arm | Number of Subjects Who Had a Decrease in HIV RNA Per Million CD4+ T Cells in the Ileum | 5 participants |
Secondary
Average Change in Activated (CD38+HLADR+) CD8+ T Cells in the Ileum
Average of changes(week 0-week 12) in the % of CD8+ T cells that are CD38+HLA-DR+, by flow cytometry
Time frame: 12 weeks
Population: All patients who had endoscopy at week 12.
| Arm | Measure | Value (MEAN) | Dispersion |
|---|---|---|---|
| Intensification Arm | Average Change in Activated (CD38+HLADR+) CD8+ T Cells in the Ileum | -5.4 percentage change | Standard Error 4.5 |
Secondary
Number of Subjects Who Experienced an Increase in CD4% in the Ileum.
Number of subjects who experienced an increase from week 0 to week 12 in CD4+ T cells (as a % of T cells, by flow cytometry) in the ileum
Time frame: 12 weeks
Population: Includes all those who had endoscopy at week 12
| Arm | Measure | Value (NUMBER) |
|---|---|---|
| Intensification Arm | Number of Subjects Who Experienced an Increase in CD4% in the Ileum. | 5 participants |
Secondary
Number of Subjects Who Experienced an Increase in CD4+ T Cells (as a % of All Cells) in the Ileum.
Number of subjects who experienced an increase in CD4+ T cells (as a % of all cells) in the ileum (by flow cytometry) from week 0 to week 12.
Time frame: 12 weeks
Population: Includes all with gut samples from week 12.
| Arm | Measure | Value (NUMBER) |
|---|---|---|
| Intensification Arm | Number of Subjects Who Experienced an Increase in CD4+ T Cells (as a % of All Cells) in the Ileum. | 6 participants |