HIV Expression in Patients With Low Viral Load on Highly Active Antiretroviral Therapy (HAART)
| Status: | Completed |
|---|---|
| Conditions: | HIV / AIDS |
| Therapuetic Areas: | Immunology / Infectious Diseases |
| Healthy: | No |
| Age Range: | 18 - Any |
| Updated: | 10/8/2017 |
| Start Date: | July 26, 2002 |
| End Date: | February 7, 2013 |
HIV Expression in Patients With Viral Loads Suppressed on HAART
This study will investigate low-level viral loads in HIV-infected patients taking highly
active antiretroviral therapy (HAART). Although HAART reduces viral levels and restores
immune function to some degree, it does not cure HIV infection. The virus persists even at
levels below that which it can be detected. This study will examine where this residual virus
comes from in order to better understand the infection and the effectiveness of therapies. In
addition, the study will 1) evaluate the ability of a new test to detect the virus at low
levels; and 2) determine whether adding the protease inhibitor Kaletra to the HAART treatment
regimen for patients with a low viral load will further decrease their viral load.
HIV-infected patients 18 years of age and older may be eligible for this study. Patients
involved in the viral load test will be recruited from an NIAID HIV study in which they are
already participating. Three groups of patients will be enrolled: those with a viral load of
less than 50 copies/ml plasma, those with 51-500 copies/ml, and those with 501-5000
copies/ml. Patients involved in the Kaletra trial must have been taking HAART for 6 months or
more and have less than 50 viral copies/ml plasma. They will be screened for this study with
a history, physical examination, and routine laboratory tests.
Participants in the viral load test evaluation will donate 70 ml of blood up to four times.
No more than one sample will be collected per day.
Participants in the Kaletra trial will have blood samples drawn on two successive days and
will then be randomly assigned to one of two treatment groups. One group will begin Kaletra
therapy (four capsules two times a day) immediately; the other will undergo observation for 4
weeks before starting Kaletra. Depending on what group they are in, patients will provide
blood samples for viral load measurements and clinical samples according to the following
schedule:
Immediate Kaletra
One sample each during weeks 1, 2, and 3, of therapy and two samples during week 4.
Delayed Kaletra
One sample each during weeks 1, 2, and 3 of observation and two samples during week 4. After
starting therapy, one sample will be collected each week during weeks 1, 2, and 3 of therapy
and two samples during week 4.
In both groups, after the last dose of medicine on day 28, Kaletra therapy will be complete.
At the end of therapy, additional blood will be collected for viral sampling as follows: one
sample each during weeks 1, 2, and 3, and two samples during week 4 after Kaletra therapy.
active antiretroviral therapy (HAART). Although HAART reduces viral levels and restores
immune function to some degree, it does not cure HIV infection. The virus persists even at
levels below that which it can be detected. This study will examine where this residual virus
comes from in order to better understand the infection and the effectiveness of therapies. In
addition, the study will 1) evaluate the ability of a new test to detect the virus at low
levels; and 2) determine whether adding the protease inhibitor Kaletra to the HAART treatment
regimen for patients with a low viral load will further decrease their viral load.
HIV-infected patients 18 years of age and older may be eligible for this study. Patients
involved in the viral load test will be recruited from an NIAID HIV study in which they are
already participating. Three groups of patients will be enrolled: those with a viral load of
less than 50 copies/ml plasma, those with 51-500 copies/ml, and those with 501-5000
copies/ml. Patients involved in the Kaletra trial must have been taking HAART for 6 months or
more and have less than 50 viral copies/ml plasma. They will be screened for this study with
a history, physical examination, and routine laboratory tests.
Participants in the viral load test evaluation will donate 70 ml of blood up to four times.
No more than one sample will be collected per day.
Participants in the Kaletra trial will have blood samples drawn on two successive days and
will then be randomly assigned to one of two treatment groups. One group will begin Kaletra
therapy (four capsules two times a day) immediately; the other will undergo observation for 4
weeks before starting Kaletra. Depending on what group they are in, patients will provide
blood samples for viral load measurements and clinical samples according to the following
schedule:
Immediate Kaletra
One sample each during weeks 1, 2, and 3, of therapy and two samples during week 4.
Delayed Kaletra
One sample each during weeks 1, 2, and 3 of observation and two samples during week 4. After
starting therapy, one sample will be collected each week during weeks 1, 2, and 3 of therapy
and two samples during week 4.
In both groups, after the last dose of medicine on day 28, Kaletra therapy will be complete.
At the end of therapy, additional blood will be collected for viral sampling as follows: one
sample each during weeks 1, 2, and 3, and two samples during week 4 after Kaletra therapy.
This protocol is an exploratory study of HIV expression in patients who are receiving highly
active antiviral therapy and who have low viral loads below or near the current limit of
detection (50 copies/ml plasma). Recent studies have suggested that patients with suppressed
viral loads in this low range have continued HIV expression, but the amount and the origin of
this virus remains unknown. The amount of virus expression in plasma is uncertain because the
current viral load assays are imprecise in the cutoff range of 50-75 copies/ml plasma. The
origin of the HIV found at low viral loads detected is unknown as well; two possible sources
of virus include expression from long-lived reservoirs of infected cells, and low level
spreading infection to uninfected cells. Determining the origin of HIV expression has
clinical importance; currently available HIV drug therapy will have little effect on HIV
expression from established reservoirs, but more potent HIV therapy could potentially inhibit
a spreading HIV infection.
In this study we plan two principal objectives. First, we will investigate the level of HIV
expression in plasma samples at low viral loads using a new HIV load assay with enhanced
sensitivity and precision in the viral load range of 1-100 copies. If data from the survey
confirms acceptable performance characteristics for this assay we will proceed with stage II
of the protocol. In stage II we plan to determine, in several short-term intensification
approaches to investigate whether the incorporation of an additional antiretroviral to
suppressive HAART regimens ("intensification HAART") will further suppress plasma virus. In a
small pilot study, we will plan to intensify regimens for 30 days in a nonrandomized fashion.
Secondly, we plan to study patients who are switching medications for preference or mild
toxicity. In these patients we will intensify their regimens for 30 days in an overlap
fashion, adding the new drug instead of switching medications. After 30 days of drug overlap,
we will continue the new drug and discontinue the identified antiretroviral. These initial
studies will assist in obtaining initial data and confirming the estimated sample size of a
larger, randomized study to rigorously investigate the virologic effects of drug
intensification. If these initial proof-of-concept experiments suggest that HIV may be
suppressed by intensification HAART, then we plan to expand the study in a larger controlled
trial to determine the degree of suppression possible with intensification therapy.
As a secondary objective we will investigate whether it is feasible to study HIV genetic
variation in samples from patients with suppressed viral loads using molecular techniques
developed to study HIV variation in patients with viral loads greater than 1000 copies/ml
plasma (protocol 00-I-0110).
We plan to enroll up to 70 patients in a viral load survey cohort of HIV viral loads, and
analyze a series of samples from completed trials of antiretroviral therapy.
active antiviral therapy and who have low viral loads below or near the current limit of
detection (50 copies/ml plasma). Recent studies have suggested that patients with suppressed
viral loads in this low range have continued HIV expression, but the amount and the origin of
this virus remains unknown. The amount of virus expression in plasma is uncertain because the
current viral load assays are imprecise in the cutoff range of 50-75 copies/ml plasma. The
origin of the HIV found at low viral loads detected is unknown as well; two possible sources
of virus include expression from long-lived reservoirs of infected cells, and low level
spreading infection to uninfected cells. Determining the origin of HIV expression has
clinical importance; currently available HIV drug therapy will have little effect on HIV
expression from established reservoirs, but more potent HIV therapy could potentially inhibit
a spreading HIV infection.
In this study we plan two principal objectives. First, we will investigate the level of HIV
expression in plasma samples at low viral loads using a new HIV load assay with enhanced
sensitivity and precision in the viral load range of 1-100 copies. If data from the survey
confirms acceptable performance characteristics for this assay we will proceed with stage II
of the protocol. In stage II we plan to determine, in several short-term intensification
approaches to investigate whether the incorporation of an additional antiretroviral to
suppressive HAART regimens ("intensification HAART") will further suppress plasma virus. In a
small pilot study, we will plan to intensify regimens for 30 days in a nonrandomized fashion.
Secondly, we plan to study patients who are switching medications for preference or mild
toxicity. In these patients we will intensify their regimens for 30 days in an overlap
fashion, adding the new drug instead of switching medications. After 30 days of drug overlap,
we will continue the new drug and discontinue the identified antiretroviral. These initial
studies will assist in obtaining initial data and confirming the estimated sample size of a
larger, randomized study to rigorously investigate the virologic effects of drug
intensification. If these initial proof-of-concept experiments suggest that HIV may be
suppressed by intensification HAART, then we plan to expand the study in a larger controlled
trial to determine the degree of suppression possible with intensification therapy.
As a secondary objective we will investigate whether it is feasible to study HIV genetic
variation in samples from patients with suppressed viral loads using molecular techniques
developed to study HIV variation in patients with viral loads greater than 1000 copies/ml
plasma (protocol 00-I-0110).
We plan to enroll up to 70 patients in a viral load survey cohort of HIV viral loads, and
analyze a series of samples from completed trials of antiretroviral therapy.
- INCLUSION CRITERIA: VIRAL SURVEY COHORT
- HIV-1 infection documented by HIV ELISA and WB
- Age greater than or equal to 18 years old
- Hemoglobin greater than or equal to 12 mg/dl within the last six weeks
- On HAART according to current DHHS guidelines.
- Most recent viral load (within the last 12 weeks):
- less than 50 by bDNA or RT-PCR (65 patients)
- 50-500 by bDNA or RT-PCR (3 patients)
- 501 - 10,000 by bDNA or RT-PCR (2 patients)
EXCLUSION CRITERIA:
-Any febrile illness (T greater than 38.0 degrees C) in the 3 weeks prior to blood draw.
VIRAL SURVEY COHORT- M98-863, M97-720, AACTG 5201 SAMPLES (no inclusion/exclusion):
-Samples from patients enrolled in the completed M98-863, M97-720 or AACTG 5201 study.
INCLUSION CRITERIA: PILOT INTENSIFICATION COHORT:
- HIV-1 infection documented by HIV ELISA and WB
- Age greater than or equal to 18 years old
- Hgb greater than or equal to 12 mg/dl
- CD4 greater than 200 cells/ micro liter and CD4% greater than 14% and not requiring
prophylaxis for opportunistic infections
- Therapy with accept HAART regimen for greater than or equal to 6 months
- Viral load less than 50 copies RNA/ml plasma by RT-PCR for at least four months
- Viral load greater than 0.38 copies RNA/ml plasma by SCA assay or positive in the
adapted Amplicor assay
- Current HAART with DHHS-approved regimen NRTI+PI, NRTI alone, NRTI+NNRTI.
- Willingness to take an additional antiretroviral to current regimen for 30 days.
- For patients to start lopinavir/ritonavir, willingness to reduce the dose of
sildenafil and other co-administered medicines that may be affected by the addition of
lopinavir/ritonavir during the course of therapy with lopinavir/ritonavir
- For patients to start efavirenz arm, willingness to take efavirenz and adjust other
medications or supplements as necessary, and to be aware that efavirenz is
contraindicated in pregnancy and that may result in false positive urine tests for THC
- For patients starting raltegravir, no prior history of rhabdomyolysis and no
co-administration of agents which, in the opinion of the investigators, would cause
rhabodomyolysis or myopathy.
- Patient must have primary care outside this protocol.
- Patients must practice accepted barrier methods to prevent pregnancy.
- For patients enrolled in piolt study of suppression after development of resistance,
patient must have documented evidence of prior drug resistance either: Prior
resisteance testing with the presence of resisnce mutations or documents evidence of
viral RNA levels greater than 100 copies/ml plasma for greater than 6 months despite
antiretroviral thereapy. Patients with prior therapy on monotherapy or suboptimal
combination therapy ARE eligible for this study.
INCLUSION CRITERIA: RANDOMIZED INTENSIFICATION COHORT (NIH, University of Pittsburgh):
- HIV-1 infection documented by HIV ELISA and WB
- Age greater than or equal to 18 years old
- Hgb greater than or equal to 12 mg/dl
- CD4 greater than 200 cells/ micro liter and CD4% greater than 14% and not requiring
prophylaxis for opportunistic infections
- Therapy with accepted HAART regimen for greater than or equal to 6 months.
- Viral load less than 50 copies RNA /ml plasma by RT-PCR for at least four months.
- Viral load greater than or equal to 0.38 copies RNA/ml plasma by SCA assay or positive
in the adapted Amplicor assay
- Current HAART with DHHS-approved regimen NRTI+PI, NRTI alone, NRTI+NNRTI.
- Willingness to take an additional antiretroviral to current regimen for 30 days.
- For patients to start lopinavir/ritonavir, willingness to reduce the dose of
sildenafil and other co-administered medicines that may be affected by the addition of
lopinavir/ritonavir during the course of therapy with lopinavir/ritonavir
- For patients to start efavirenz arm, willingness to take efavirenz and adjust other
medications or supplements as necessary, and to be aware that efavirenz is
contraindicated in pregnancy and that may result in false positive urine tests for THC
- Patient must have primary care outside this protocol.
- Patients must practice accepted barrier methods to prevent pregnancy.
EXCLUSION CRITERIA:
- Requirement for cytotoxic agents including hydroxyurea or vaccinations during the
study period
- Chronic corticosteroid therapy
- Concurrent therapy with investigational cytokines including IL-2 or IL-12 during the
course of the study. Prior administration of cytokines is not an exclusion criteria;
at least 4 months from most recent cycle of IL-2 or IL-12. GCSF and erythropoietin
therapy will be permitted
- History of taking a salvage regimen; i.e., patient has had clinical resistance to
antiretrovirals. Changing antiviral therapy because of adverse effects is permitted
- Prior PI therapy or NNRTI therapy is not permitted unless the previous PI-containing
therapy was switched because of patient preference. If the patient has a documented
history of lipid elevations (fasting triglycerides greater than 750 mg/dl), the
patient will not be eligible for PI addition.
- Any febrile illness (T greater than 38.0 degrees C) in the 3 weeks prior to enrollment
- Any vaccination in the 6 weeks prior to enrollment
- Current pregnancy or lactation, history of pregnancy in the last 4 months
- Prior history of intolerance to the added antiretroviral
- For lopinavir/ritonavir addition, baseline elevated triglycerides greater than 400
mg/dl without lipid lowering agents
- Elevated baseline ALT liver function assays greater than 2 fold greater than upper
limit of normal
- Known history of liver disease or Child-Pugh score greater than 5.
- History of pancreatitis requiring hospitalization
- Concomitant use with drugs that are highly dependent on cytochrome P450 for clearance,
which, in the opinion of the investigators, may lead to the unexpected changes in
their concentrations occurring after the addition of lopinavir/ritonavir or efavirenz.
Examples include but are not limited to: wafarin-like anticoagulation , amiodarone,
astemizole, cisapride, statin class of drugs, gemfibrozil, cyclosporine, ergonavine,
ergotamine, methylergonavine, dihydroergotamine, dofetilide, flecanide, quinidine,
fusidic acid, methadone, demerol, midazolam, triazolam, phenytoin, dilantin, pimozide,
sirolimus, tacrolimus, propafenone, quinupristin, terfenadine, theophylline, rifampin,
rifapentene, or rifabutin and illicit substances, including the recreational substance
(ecstasy) methylenedioxymethamphetamine.
- History of chronic diarrhea or inflammatory bowel disease
- History of hemophilia
- Inability to comply with the protocol
For those starting efavirenz, significant depression, which, in the opinion of the
investigators, would be significantly worsened by efavirenz.
INCLUSION CRITERIA - DRUG OVERLAP COHORT:
- HIV-1 infection documented by HIV ELISA and WB
- Age greater than or equal to18 years old
- Hgb greater than or equal to 12 mg/dl
- CD4 greater than 200 cells/ micro liter and CD4% greater than 14% and not requiring
prophylaxis for opportunistic infections
- Therapy with accepted HAART regimen for greater than or equal to 6 months
- Viral load less than 50 copies RNA/ml plasma by RT-PCR for at least four months
- Viral load greater than 0.38 copies RNA/ml plasma by SCA assay or positive in the
adapted Amplicor assay
- Current HAART with DHHS-approved regimen NRTI+PI, NRTI alone, NRTI+NNRTI
- Willingness to take an additional antiretroviral to current regimen for 30 days
- For patients planning to start lopinavir/ritonavir, or other ritonavir containing
regimen willingness to reduce the dose of sildenafil and other co-administered
medicines that may be affected by the addition of ritonavir during the course of
therapy with lopinavir/ritonavir
- For patients to start efavirenz, willingness to take efavirenz and adjust other
medications or supplements as necessary, and to be aware that efavirenz is
contraindicated in pregnancy and that may result in false positive urine tests for THC
- Patient must have primary care outside this protocol
- Patients must practice accepted barrier methods to prevent pregnancy.
EXCLUSION CRITERIA:
- Requirement for cytotoxic agents including hydroxyurea or vaccinations during the
study period
- Chronic corticosteroid therapy
- Concurrent therapy with investigational cytokines including IL-2 or IL-12 during the
course of the study. Prior administration of cytokines is not an exclusion criteria;
at least 4 months from most recent cycle of IL-2 or IL-12. GCSF and erythropoietin
therapy will be permitted
- History of taking a salvage regimen; i.e., patient has had clinical resistance to
antiretrovirals. Changing antiviral therapy because of adverse effects is permitted
- Prior PI therapy or NNRTI therapy is not permitted unless the previous PI-containing
therapy was switched because of patient preference. If the patient has a documented
history of lipid elevations (fasting triglycerides greater than 750 mg/dl) the patient
will not be eligible for PI addition.
- Any febrile illness (T greater than 38 degrees C) in the 3 weeks prior to enrollment
- Any vaccination in the 6 weeks prior to enrollment
- Current Pregnancy or lactation, history of pregnancy in the last 4 months
- Prior history of intolerance to the added antiretroviral
- For protease addition, baseline elevated triglycerides greater than 400 mg/dl without
lipid lowering agents
- Elevated baseline ALT liver function assays greater than 2 fold greater than upper
limit of normal
- Known history of liver disease or Child-Pugh score greater than 5.
- History of pancreatitis requiring hospitalization
- For patients who are adding ritonavir or efavirenz, concomitant use with drugs that
are highly dependent on cytochrome P 450 for clearance, which, in the opinion of the
investigators, may lead to the unexpected changes in their concentrations occurring
after the new drug is added. Examples include but are not limited to: wafarin-like
anticoagulation , amiodarone, astemizole, cisapride, statin class of drugs,
gemfibrozil, cyclosporine, ergonavine, ergotamine, methylergonavine,
dihydroergotamine, dofetilide, flecanide, quinidine, fusidic acid, methadone, demerol,
midazolam, triazolam, phenytoin, dilantin, pimozide, sirolimus, tacrolimus,
propafenone, quinupristin, terfenadine, theophylline, rifampin, rifapentene, or
rifabutin and illicit substances, including the recreational substance (ecstasy)
methylenedioxymethamphetamine
- History of chronic diarrhea or inflammatory bowel disease
- History of hemophilia
- Inability to comply with the protocol
- For those starting efavirenz, significant depression, which, in the opinion of the
investigators, would be significantly worsened by efavirenz
We found this trial at
1
site
9000 Rockville Pike
Bethesda, Maryland 20892
Bethesda, Maryland 20892
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