Data from a clinical trial involving UCLA researchers suggest that a new therapy may potentially serve as a “functional cure” for HIV/AIDS.
The therapy, called SB-728-T, involves the modification of both copies of a patient’s CCR5 gene, which encodes the major co-receptor used by HIV to infect immune system cells.
In the Sangamo BioSciences’ phase 1 trial, SB-728-T was given to HIV patients who were on highly active antiretroviral therapy (HAART) but were considered to be “non-responders” — that is, their CD4+ T-cell levels, a key measure of immune system health, remained low. The patients’ HAART therapy was interrupted when they received the SB-728-T therapy.
The researchers found a statistically significant relationship between the suppression of HIV viral load and the level of circulating CD4+ T-cells that had undergone the CCR5 gene modification in patients treated with SB-728-T.
The scientists recently presented these and others findings from their dose-escalation study (SB-728-902) at the 51st Interscience Conference on Antimicrobial Agents and Chemotherapy, held from Sept. 17 to 20 in Chicago. The study involves subjects on HAART whose CD4+ counts remain below 500 cells per cubic millimeter — and below 450 cells in one cohort — after several years of therapy.
“We are very encouraged by both this early demonstration of an antiviral effect of SB-728-T, as well as the marked improvement in the overall CD4+ T-cell counts in treated subjects in the SB-728-902 trial,” said Dr. Ronald Mitsuyasu, a principal investigator for the study who directs the UCLA Center for Clinical AIDS Research and Education and is an associate director of the UCLA AIDS Institute. “While their viral loads are well controlled on HAART, these subjects experienced incomplete restoration of their T-cell counts. Improvement and preservation of the immune system is of paramount importance in HIV, and those seen in this study show an improvement over that seen after several years of HAART.”
The modification of the CCR5 gene that generates SB-728-T is accomplished using a zinc finger nuclease, or ZFN. ZFN modification disrupts the expression of this key co-receptor for HIV entry and renders cells resistant to HIV infection. The approach is based on the observation that a naturally occurring mutation in the CCR5 gene, CCR5 delta-32, provides protection from HIV infection.
Individuals who have the delta-32 mutation in both copies of the CCR5 gene are generally not susceptible to the most common strain of HIV. Those with only one copy of the mutation are identified as “elite controllers” because of their immune systems’ ability to resist the progression of HIV without the need for HAART.
Other findings described by the scientists included:
- The viral load of one SB-728-T-treated subject decreased to undetectable levels during a treatment interruption. This subject was found to be an “elite controller.”
- Unprecedented improvements in overall CD4+ T-cell counts and the ration of CD4+ to CD8+ cells, as well as engraftment, expansion, trafficking and persistence of the ZFN-modified cells.
- SB-728-T treatment continues to be safe and well tolerated.
“The data obtained in our treatment-interruption studies are very exciting and represent significant progress toward a ‘functional cure’ for HIV/AIDS,” said Dr. Carl June, director of translational research at the Abramson Family Cancer Research Institute at the University of Pennsylvania School of Medicine, one of the study sites. “The statistically significant relationship between estimated modification of both copies of the CCR5 gene and viral load during the treatment interruption suggests that the next step is to increase the frequency of the modified cells in HIV-infected patients with the ultimate hope that, if we do, we will achieve a ‘functional cure’ and eliminate the need for continued HAART.”
No other drug has been shown to have the same dramatic effect on the immune system in this setting, said Dr. Dale Ando, Sangamo’s chief medical officer and vice president of therapeutic development.
“SB-728 treatment results in unprecedented improvement in immune system health, as measured by increased CD4+ T-cell levels and improved CD4+—to—CD8+ T-cell ratios, even in subjects that entered the trial with poor CD4+ counts,” Ando said. “Moreover, the interesting kinetics in viral load that we observed in the first few subjects that underwent a treatment interruption have been borne out and have allowed us to correlate a statistically significant effect of the rate of biallelic ZFN-modification of the CCR5 gene on viral load during treatment interruption.”
(Source: UCLA Health System)