Need For An HIV Cure
The worldwide epidemic of HIV/AIDS caused immeasurable suffering and challenged the biomedical community to create treatments for this devastating disease. A robust response from researchers and pharmaceutical companies led to the development of potent therapies capable of controlling HIV. These treatments were the first medicines designed to slow a viral disease and were proven to extend life span for infected individuals. Despite the remarkable impact on HIV, even decades of treatment failed to cure the disease. The HIV infection rebounds quickly when treatment is interrupted or viral drug resistance arises,
and no amount of conventional therapy has overcome this problem. Despite improvements in the medications, it is time for new treatment strategies aimed at eliminating the dependence on antiretroviral therapy. We believe these treatments can rebuild key components of immunity and provide lifelong suppression of HIV with protection against future re-infection. The challenge of rebuilding natural immunity is the inspiration for AGT’s program to develop next generation therapies for HIV disease. Our strategies use the tools of genetic medicine and depend on our deep understanding of key features in HIV disease.
Phase 1 Trial Status
AGT received approval by the FDA to begin Phase 1, the first human clinical trial for AGT's lead HIV program. The study is being conducted at clinical sites in the Baltimore/D.C. area. AGT's Phase 1 study clinicaltrials.gov identifier number is NCT04561258 and the study ID is AGT-HC168. For information about the ongoing Phase 1 study of AGT103-T, and information on the trial sites, click here.
How AGT103-T Is Intended to Work
CEO Jeff Galvin Provides an Overview of AGT’s HIV Functional Cure Project
DEPLETION OF HIV-SPECIFIC CD4 T CELLS
Finding the Achilles Heel of HIV Infection
Many viruses cause short term disease and leave behind a protective immune “memory”. Vaccines mimic this natural event by artificially triggering potent immune responses that will remain as memory for months to years, then reappear and control the infection after a natural virus exposure. For many years researchers have worked toward creating a vaccine against HIV that would trigger natural immunity and prevent infection similar to other vaccines that are critical tools for public health. Sadly, this effort has not yet been successful.
The key to vaccine failure is HIV’s preference for infecting and killing helper T cells, also known as CD4 T cells. True to their designation as “helpers”, these T cells are among the first to respond against new virus infections and they retain a memory of that response. For example, months to years after flu vaccination, any new exposure to the influenza virus activates the memory CD4 T cells and sparks the development of protective immunity and resistance to flu. These influenza-specific CD4 T cells are key to vaccine protection and must be maintained at high levels for months to years after immunization to be ready for quick and potent activation of the protective immune response.
In HIV disease, the HIV-specific CD4 T cells are activated soon after infection similar to other viral diseases. However, HIV targets these cells for destruction because this insidious virus binds to the same CD4 molecule that identifies the helper T cell subset. HIV infection, HIV-specific CD4 T cells are compromised soon after infection, eventually falling below the levels needed to support effective immunity. By that point, only antiretroviral medication is effective for controlling HIV, and infected individuals who seek treatment begin a daily drug regimen that must be continued without interruption for life.
This single feature of HIV disease, that virus depletes the HIV-specific CD4 T cells helper, explains why HIV comes roaring back after years of effective therapy if the treatment is stopped. A key piece of natural immunity to HIV is missing and there is no immune control of the virus.
Manufacturing of specific T cells is used increasingly to make treatments for infectious diseases and cancer. In most cases, the processes are straightforward and cells are highly effective after injecting back into the person suffering from disease. A new industry is springing up around the need for cell manufacturing and is providing automation of highly efficient cell processing for T cell-based products. In most cases, specific cells are purified, grown to large numbers outside the body, then injected back in as a living cell therapy using the person’s own cells so there is no risk of rejection.
AGT is using a process similar to what others are doing but critical changes were needed to generate an HIV therapy. Were we to purify HIV-specific CD4 T cells, grow them to high numbers and inject them back into the body, we would be adding fresh target cells for the virus, in essence adding fuel to the fire. We needed an extra step to protect new cells from infection so that the effects of treatment would be long-lasting and not destroyed by future exposure to HIV. The extra step was to create a viral vector capable of introducing protective genes into the HIV-specific CD4 T cells. Total T cells are purified from blood and stimulated to grow the HIV-specific CD4 T cells which are treated with viral vector (lentivirus vector AGT103) to protect them against HIV infection and destruction. The lentivirus vector inserts genes for HIV protection into the chromosomal DNA of each cell. This process creates a permanent modification capable of reducing cell surface expression of CCR5 protein (a co-receptor for HIV attachment/entry) and attacking HIV RNA in the regions known as Vif or Tat viral genes.
Manufacturing Cell Products for Treatment of HIV Disease
We developed a highly efficient, cost-effective process for manufacturing large numbers of HIV-specific cells, modifying them with lentivirus vector AGT103, and infusing them back into the body as a single dose, autologous cell therapy. Three key features of the AGT103-T product are:
The lentivirus vector modifies HIV-specific CD4 T cells and: prevents infection by CCR5- or CXCR4-tropic strains of HIV; reduces depletion of CD4 T cells during exposure to HIV; and prevents a latently-infected cell from releasing new HIV virus particles
The process for cell manufacturing is reliable and consistent; this is important for supporting clinical trials
AGT103-T starts with about 1 million HIV-specific CD4 T cells obtained from blood and, by the end of production, delivers about 1 billion HIV-specific CD4 T cells with most of them modified by the AGT103 lentivirus vector
By achieving this high dose of HIV-specific CD4 T cells that are protected from attack by HIV, we expect this treatment to reconstitute the immune system and restore an ability to make antiviral immune responses for natural control of HIV. Our upcoming human clinical trials are the first step in testing this concept.
Status of the Clinical Trial
These Two HIV+ Clinical Trial Participants Believe In HIV Cure Research
Watch Their Video Testimony
Our Commitment to Developing New Treatments for HIV
Our company is developing genetic medicines for unmet medical needs. First among our priorities is a treatment for HIV that restores natural control of viremia and reduces dependence on antiretroviral therapy. We believe natural virus control will be effective and will reduce the costs and side-effects inherent in life-long use of antiretroviral medication. Please see below, the views of our Chief Science Officer David Pauza, and one of our clinical advisors Dr. Ely Benaim, regarding the importance of AGT’s program for HIV therapy.
100% GOES TO PHASE 1 PATIENT CLINICAL CARE
You Can Help Support the Clinical Trial Today
Our HIV cure program clinical trial has just started! Unlike big Pharma, we don’t have billion-dollar reserves to draw from. Instead, we rely solely on investments to fund our research. We've created a way that you can help!