- Category: Search for a Cure
- Published on Friday, 07 March 2014 00:00
- Written by Liz Highleyman
Genetically modified CD4 T-cells lacking CCR5 co-receptors reach high levels in the body and are resistant to HIV infection, potentially enabling people to maintain a low viral load while off antiretroviral therapy (ART), according to the latest reports from studies evaluating Sangamo Biosciences' SB-728-T zinc finger gene therapy technology.
Pre-treating patients with the cancer chemotherapy drug cyclophosphamide (Cytoxan) promotes proliferation and activity of the modified T-cells, and people receiving the highest dose saw the greatest reductions in HIV viral load during ART interruption, according to a presentation at the 21st Conference on Retroviruses and Opportunistic Infections (CROI 2014) this week in Boston. A concurrent report in the New England Journal of Medicine describes outcomes from the first in this series of trials, including a participant with controlled viral load during an extended ART interruption.
Sangamo developed a technique that uses a zinc finger nuclease to disruptthe gene in CD4 T-cells that controls expression of CCR5, the co-receptor that most strains of HIV use to enter cells.
People with two copies of a naturally occurring genetic mutation called CCR5-delta-32 do not produce this co-receptor and are resistant to HIV infection. A man known as the Berlin Patient appears to remain free of HIV 7 years after receiving transplanted bone marrow stem cells (which give rise to all blood cells) from a donor with this mutation.
In clinical trials of this approach, samples of CD4 T-cells are collected from HIV-positive participants, treated with the zinc finger protein in a laboratory, and allowed to multiply. The modified cells, called SB-728-T, are then re-infused back into the same patient. The idea is that these modified cells -- being protected from HIV entry -- will persist, while normal T-cells are killed off by the virus.
This technique has been tested in several cohorts, including people who have not achieved good CD4 cell recovery despite viral suppression on ART and people who carry a single copy of the natural CCR5-delta-32 mutation, known as heterozygotes.
Researchers have previously reported that the gene therapy procedure is safe and generally well tolerated. The modified SB-728-T cells proliferate and distribute themselves throughout the body like normal T-cells. Study participants experienced substantial CD4 cell gains and decreased virus levels associated with bi-allelic or double-copy gene modification.
The study presented at the Retrovirus Conference by Gary Blick from the Circle Care Center in Norwalk, CT, evaluated the effect of pre-conditioning with cyclophosphamide prior to re-infusion of modified SB-728-T cells.
The rationale is that killing off some normal T-cells "makes room" for the altered cells. Used in treatment of cancer and autoimmune diseases, cyclophosphamide enhanceshomeostatic proliferation of transferred T-cells, increases levels of certain cytokines, and promotes migration of new T-cells to lymphoid organs.
This open-label dose-escalation study (SB-728-1101) included 12 participants, all but 1 men. At study entry they had high CD4 T-cell counts (500-1300 cells/mm3) and undetectable viral load on a stable ART regimen.
Participants received intravenous cyclophosphamide at doses of 200, 500 or 1000 mg/m2 given 1 to 3 days prior to a single infusion of approximately 10-40 billion modified T-cells. After 6 weeks they started an analytic ART treatment interruption. The interruption was planned to last 16 weeks, but could be extended if a patient maintained a viral load below 10,000 copies/mL and a CD4 count above 500 cells/mm3.
- Study participants showed evidence of extensive engraftment of bi-allelic modified T-cells.
- Both total CD4 counts and numbers of modified cells increased in a dose-dependent manner, with the largest gains seen in the 1000 mg dose group.
- Most participants saw their viral load decrease during ART interruption.
- 1 patient in the 200 mg group and 2 people in the 500 mg group had HIV RNA declines of nearly 1.0 log.
- 1 participant in the 1000 mg group saw a viral load drop of 1.9 log; this individual remains off ART with detectable but low and stable viral load.
- Cyclophosphamide was generally safe and well-tolerated.
- Some patients experienced nausea, especially at higher doses, but this was successfully managed with anti-emetic drugs.
- There were no clinically significant decreases in neutrophils, various white blood cells, red blood cells, or platelets.
"Cytoxan conditioning may be a useful strategy to maximize the engraftment and anti-viral effects of SB-728-T adoptive T-cell therapy in HIV subjects and may be an important immunomodulatory chemotherapeutic agent for immunotherapy in HIV," the researchers concluded.
The researchers noted that the level of bi-allelic modified T-cell engraftment in patients taking the 1000 mg cyclophosphamide dose was near levels associated with HIV protection in natural CCR5-delta-32 heterozygous individuals.
Blick further explained at a CROI media briefing that the 1000 mg dose appears to approach the threshold for a functional cure, leading the researchers to look at a higher dose of 1500 mg to see if they can push up response rates further without unacceptable toxicity. "We can probably get a functional cure if we get enough engraftment," Blick said.
Extended ART Interruption
Data from the first Phase 1 trial of the SB-728-T approach in humans was published in the March 6, 2014, New England Journal of Medicine.
In this open-label proof-of-concept study (SB-728-902), Pablo Tebas and Carl June from the University of Pennsylvania and colleagues enrolled 12 people with HIV who had undetectable viral load on ART. They were divided into 2 cohorts, one with good CD4 cell recovery on ART (>450 cells/mm3), the other with poor immunological recovery (200-500 cells/mm3).
Participants received a single infusion of approximately 10 billion zinc finger-treated autologous or self-donated T-cells, with 11% to 28% of cells successfully modified (cyclophosphamide was not used in this study). After 4 weeks, patients in the first group underwent planned ART interruption, while poor CD4 responders remained on treatment.
The median CD4 T-cell count rose significantly, reaching a median of about 1500 cells/mm3 from the pre-infusion level of about 450 cells/mm3. After 1 week, the median concentration of CCR5-modified T-cells was 250 cells/mm3, comprising 14% of circulating CD4 T-cells and 9% of circulating peripheral blood mononuclear cells.
The half-life of modified cells was 48 weeks. Modified cells declined by about 2 cells per day while off ART, compared with a decrease of about 7 cells/day for unmodified cells, showing that the altered cells lacking CCR5 had a survival advantage.
Several participants experienced viral load reductions during ART interruption, including one whose HIV RNA became undetectable. This individual was found to be CCR5-delta-32 heterozygous, meaning he naturally had some cells lacking the co-receptor. This participant maintained viral control for 31 weeks without ART and remains off treatment.
The modified T-cell technique appeared safe in the short term, with just 1 patient experiencing a transient transfusion reaction with low-grade fever and chills.
In summary, this study showed that modified SB-728-T cells persist and appear to have a selective advantage over unmodified cells when exposed to HIV during ART interruption.
"Our experience reinforces our belief that an immunological approach is a promising approach to enable functional control of HIV infection and eliminate the need for lifelong ART," June said in a press release issued by Sangamo.
The release also noted that the company has developed a new process to deliver the zinc finger nuclease using mRNA instead of an adenovirus vector, which will allow recipients to be retreated if necessary.
G Blick, J Lalezari, R Hsu, D Ando, et al. Cyclophosphamide Enhances SB-728-T Engraftment To Levels Associated With HIV-RNA Control. Conference on Retroviruses and Opportunistic Infections (CROI 2014). Boston, March 3-6. Abstract 141.
P Tebas, D Stein, WW Tang, C June, et al. Gene Editing of CCR5 in Autologous CD4 T Cells of Persons Infected with HIV. New England Journal of Medicine 370(10):901-910. March 6, 2014.
Sangamo Biosciences. Sangamo Presents Clinical Data at CROI 2014 Demonstrating Enhancement of SB-728-T Engraftment -- Continued Control of HIV Viral Load for 31 Weeks Without ART in SB-728-T Treated Subject. Press release. March 6, 2014.
Sangamo Biosciences. First-In-Man Study Of Genome Editing Using Sangamo's ZFN Technology Published In New England Journal Of Medicine. Press release. March 5, 2014.
National Institutes of Health. Genetic Modification of Cells Proves Generally Safe as HIV Treatment Strategy. Press release. March 5, 2014.