The availability of antiretroviral therapy (cART) for HIV-1 infection has led to a reduction in morbidity in patients with chronic HIV infection. However, cART does not eliminate HIV-1 that persists as a latent infection in cellular reservoirs. Usually, HIV viremia rapidly rebounds if antiretroviral therapy is interrupted. Consequently, HIV infected individuals must commit to expensive, life-long therapies and must tackle problems associated with chronic infection and uninterrupted cART, including continuous clinical and laboratory monitoring, drug toxicities, and chronic immune activation/inflammation. Currently, there is an emerging interest in developing safe and affordable curative strategies that would eliminate the need for lifelong therapy. However, to date only allogeneic hematopoietic stem cell transplantation (allo-HSCT) has shown results in decreasing the HIV-1 reservoirs. The IciStem Consortium (www.icistem.org) has assembled the largest and most exhaustive observational cohort for the study of HIV reservoir dynamics in allo-HSCT HIV+ individuals with severe hematological malignancies worldwide. Within the cohort, only individuals transplanted with a donor with thw CCR5A32 mutation have shown signs of HIV remission. On the other side broadly neutralizing antibodies (bNAbs) have shown the potential to control HIV infection. This study intends to evaluate if the allo-HSCT combined with the additional application of bNAbs is effective to control HIV replication.
The availability of antiretroviral therapy (cART) for HIV-1 infection has led to a reduction in morbidity in patients with chronic HIV infection. However, cART does not eliminate HIV-1 that persists as a latent infection in cellular reservoirs. Usually, HIV viremia rapidly rebounds if antiretroviral therapy is interrupted. Consequently, HIV infected individuals must commit to expensive, life-long therapies and must tackle problems associated with chronic infection and uninterrupted cART, including continuous clinical and laboratory monitoring, drug toxicities, and chronic immune activation/inflammation. Currently, there is an emerging interest in developing safe and affordable curative strategies that would eliminate the need for lifelong therapy. However, to date only allogeneic hematopoietic stem cell transplantation (allo-HSCT) has shown results in decreasing the HIV-1 reservoirs. The IciStem Consortium (www.icistem.org) has assembled the largest and most exhaustive observational cohort for the study of HIV reservoir dynamics in allo-HSCT HIV+ individuals with severe hematological malignancies worldwide. Within the cohort, only individuals transplanted with a donor with thw CCR5A32 mutation have shown signs of HIV remission. On the other side broadly neutralizing antibodies (bNAbs) have shown the potential to control HIV infection. This study intends to evaluate if the allo-HSCT combined with the additional application of bNAbs is effective to control HIV replication. Detailed Description: The implementation of highly effective, convenient, and well-tolerated combination antiretroviral therapy (cART) for HIV-1 infection has substantially reduced AIDS-related morbidity and mortality. However, cART does not eliminate HIV-1 that persists as a latent infection in cellular reservoirs, including resting memory CD4+ T cells, leading to an underlying raised state of immune activation and subsequent immune senescence. Of note, HIV viremia rapidly rebounds if antiretroviral therapy is interrupted. Consequently, HIV infected individuals must commit to expensive, life-long therapies and must tackle problems associated with chronic infection and uninterrupted cART, including continuous clinical and laboratory monitoring, drug toxicities, and chronic immune activation/inflammation. Therefore, there is an emerging interest in developing safe and affordable curative strategies that would eliminate the need for lifelong therapy while improving the health of infected subjects and reducing the risk of viral transmission to uninfected individuals. So far, allogeneic hematopoietic stem cell transplantation (allo-HSCT) is the only intervention to date that systematically reduces HIV-1 reservoirs to undetectable levels regardless of the CCR5Δ32 donor status. IciStem is a prospective observational project to investigate cases of allo-HSCT in HIV-1-infected individuals and their putative remission. Over the last few years, the IciStem Consortium (www.icistem.org) has assembled the largest and most exhaustive observational cohort for the study of HIV reservoir dynamics in allo-HSCT HIV+ individuals with severe hematological malignancies worldwide. 39 individuals have already been transplanted and followed up in the IciStem cohort and subsequent undetectable HIV reservoirs in blood and tissues have been described in those with 100% chimerism while still on antiretroviral treatment (ART). Detailed analysis of CCR5wt allo-HSCT cases within the IciStem cohort has provided insights on additional factors such as conditioning regimen, total body irradiation, graft versus host disease, and viral tropism that contribute to eradication of the potentially infectious viral reservoir in addition to the lack of a functional CCR5 receptor. Allo-HSCT has proved a profound effect on the HIV reservoir. So far, only participants with homozygous CCR5Δ32 mutation have shown signs of HIV remission whereas participants without the CCR5Δ32 mutation had a delayed rebound during ATI. bNAbs have shown the potential to control HIV infection. Consequently, the combination of allo-HSCT with these antibodies is one of the aims of the study by which new cases of HIV remission might be achieved in this setting. During the last 48 months IciStem has generated a prospective observational cohort of 39 cases of allo-HSCT in HIV-positive participants with severe hematological malignancies in 21 clinical sites in 9 countries (Europe and Canada). Those 39 cases (from the 45 registered) have been followed up with continuous sample collection and high-resolution state of the art virological and immunological analysis. A summary of preliminary studies and achievements is listed below 1. Nine transplants involved CCR5Δ32/Δ32 donors, and 18 involved CCR5wt donors. 2. Mean post-HSCT follow-up is 1656 days, with 18 participants alive in active follow-up (4 transplanted with CCRΔ32/Δ32 donor); 13 IciStem participants are beyond the 2nd year post-HSCT, respectively. From those, 8 are out of immune suppression and with minimal-undetectable HIV latent reservoirs. 3. Five participants from the IciStem Cohort are currently suitable to enter in the first ITATI approach within the IciStem core. Those 5 participants have no detectable replication competent HIV reservoir in presence of cART and have been followed up for the longest time. The therapeutically intervention for these participants will be an analytical treatment interruption with additional application of broadly neutralizing antibodies (bNAbs) that recently have been described as safe and effective to control HIV replication in infected participants. The rationale for application of these bNAbs during the treatment interruption of the IciStem participants: * To help prevent viral rebound in absence of cART, due to their proven capacity to potently and durably suppress any possible residual HIV replication * To rapidly eliminate a cell producing virus via mechanisms such as ADCC (Antibody dependent cellular cytotoxicity) * To facilitate the development of a broad CTL (Cytotoxic T lymphocytes) response sufficient to maintain remission, as demonstrated in macaques/SHIV studies (Nishimura, 2017) * To protect the individuals from a putative viral rebound with a safe system, as bNAbs application has few side effects and rarely causes adverse events * To achieve a highly specific targeting and inhibition of HIV to avoid massive overall bystander activation of the immune system that in effect could lead to a higher chance of HIV reinfection of activated CD4+ T cells. Despite cART has substantially reduced HIV-related morbidity and mortality, HIV reservoirs are still present and represent a key concern currently for HIV remission. This fact has resulted in a chronicity of HIV infection, leading to emotional disturbances and psychological burden associated with this perpetuation of the disease in the daily living. In the setting of HIV eradication trials, analytical interruption of antiretroviral therapy is a requirement to investigate HIV remission, control, and potential viral rebound. However, discontinuation of cART is linked to psychological issues that should be considered in the setting of HIV cure trials: 1. Stopping cART may lead to variable clinical detriments. Those detriments may induce worry and psychological distress, which can not only worsen the quality of life, but also cause an instability of the emotional status. At the same time, that breakdown of the emotional system may influence the clinical status. Even when clinical consequences are not manifested or self-perceived, beliefs about unfavorable health-related results and desperation for HIV remission may arise. 2. Interrupting cART may increase the risk to infect other people. Those who discontinue cART may not be willing therefore to put their sexual partners at risk. Even after deciding to participate and to interrupt cART, they may develop worries and fears about infecting others. 3. This sort of HIV remission trial comprises a very specific collective of people. People who have suffered from a hematologic medical complication indicative for stem cell transplantation and have survived this severe health problem. This fact already indicates an impacted emotional status (without even considering the ITATI). Besides, specifically in the current study, additional medical strategies will be applied. Those interventions will be new for the participants (i.e., immune therapy) and will require multiple additional medical appointments. Those characteristics add complexity to the psychological management during the participation in the study. For all the reasons presented, the participants' psychological predisposition to ITATI and the participation in the study and the emotional status will be monitored carefully throughout the trial. This will be managed at 2 levels: first by continuous assessment of the emotional status and second by offering emotional support whenever required, especially considering the cessation of cART and initiation of the immune therapy.
Study Type
INTERVENTIONAL
Allocation
NA
Purpose
HEALTH_SERVICES_RESEARCH
Masking
NONE
The participant will perform an Analytical Treatment Interruption (ATI) of up to 18 months of duration. During the first 8 months, the participants will be infused once per month with a combination of the broadly neutralizing antibodies (bNAbs) 3BNC117 and 10-1074
Fondazione IRCCS Ca' Granda Ospedale Maggiore Policlinico di Milano
Milan, Lombardy, Italy
University Medical Center Utrecht
Utrecht, Netherlands
Complejo Hospitalario Universitario de Granada
Granada, Andalusia, Spain
Hospital Gregorio Marañón
Madrid, Spain
Time to reappearance of HIV-1 viremia
Time to reappearance of HIV-1 viremia (plasma HIV-1 RNA level \> 50 copies/ml in 2 consecutive measurements) after ART interruption.
Time frame: From Baseline to 18 months
Time to reappearance of HIV-1 replication competent reservoir
Time to reappearance of HIV-1 replication competent reservoir (determined by the number of infectious units per 106 CD4+ T cells (IUPM) using a viral outgrowth assay) after ART interruption.
Time frame: From Baseline to 18 months
Time to reappearance of HIV-1 total reservoir
Time to reappearance of HIV-1 total reservoir (determined by the number HIV-DNA copies per 106 CD4+ T cells using ddPCR) after ART interruption.
Time frame: From Baseline to 18 months
Rate and severity of adverse events (AE) and serious adverse events (SAE)
Safety evaluation, as measured by rate and severity of adverse events (AE) and serious adverse events (SAE).
Time frame: From Baseline to 18 months
Serum levels of 3BNC117 and 10-1074
Serum levels of 3BNC117 and 10-1074 throughout the study
Time frame: From Baseline to 18 months
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