Armed with a novel strategy they developed for bolstering the body’s immune response, scientists at Albert Einstein College of Medicine have successfully suppressed HIV infections in mice—offering a path to a functional cure for HIV and other chronic viral infections. Their findings were published in the Journal of Clinical Investigation.
The research involved proteins designed to selectively stimulate the immune system’s CD8+ “killer” T cells to multiply and specifically attack HIV-infected T cells. Co-corresponding author Steven Almo, developed the synthetic proteins, known as synTac (short for “synapse for T-cell activation”).
HIV infects the immune system’s CD4+ T cells. For the past 25 years, people infected with HIV have been able to control their infection through antiretroviral therapy (ART)—a combination of several drugs that prevent HIV from infecting new CD4+ T cells and multiplying within them.
“Although ART works remarkably well at keeping HIV in check indefinitely, it is a stalemate and not a checkmate,” said co-corresponding author Harris Goldstein, M.D., director of the Einstein-Rockefeller-CUNY Center for AIDS Research. “ART’s long-term use can cause substantial side effects,” noted Goldstein. “And once ART is halted, latent HIV viruses—which can persist for years in CD4+ T cells—invariably emerge from their hiding places to revive the infection. Our JCI paper shows that synTac proteins, by greatly boosting the quantity of protective HIV-specific CD8+ T cells, were able to eliminate these infected cells.
“It’s unlikely that any treatment strategy can remove all latently infected T cells,” Goldstein continued. “Our goal with synTac is a ‘functional cure,’ in which the powerful immune response induced by synTac suppresses HIV to undetectable levels even after they discontinue ART.”
The researchers first tested their anti-HIV synTac proteins on human blood samples infected with either HIV or cytomegalovirus (CMV), a common type of herpes virus that can infect and kill immunosuppressed patients. For blood from human donors infected with either HIV or CMV, synTacs specific for mobilizing immune responses against those viruses triggered selective and vigorous multiplication of CD8+ T cells that exhibited potent HIV or CMV anti-viral activity.
Next, the researchers intravenously injected synTacs specific for HIV or CMV into virus-infected mice with “humanized” immune systems that permit infection by viruses affecting people, such as HIV and CMV. The synTac proteins triggered human HIV-specific CD8+ T cells to increase 32-fold and increased human CMV-specific CD8+ T cells by 46-fold. In both the HIV- and CMV-infected mice, the large numbers of synTac-stimulated human CD8+ T cells potently suppressed the viral infections—suggesting that synTacs may offer new opportunities for functionally curing HIV and treating CMV and other viral infections.
“A key asset of the synTac platform,” said Almo, “is how easily we can program synTac proteins to combat any of the many diseases in which T cells play a role—including disease targets that extend well beyond viruses. For example, an ongoing clinical trial involving patients with head and neck cancer is assessing synTac’s ability to selectively activate anti-cancer T cells. And since synTacs can turn off, as well as activate T cells, they’re also under study for treating type 1 diabetes and other autoimmune diseases by turning off T cells that mistakenly attack people’s healthy tissues.”
Republished courtesy of Albert Einstein College of Medicine.