Can Gene Therapy Offer a Permanent Solution for HIV?

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Can Gene Therapy Offer a Permanent Solution for HIV?

Synopsis

A groundbreaking study from Johns Hopkins University reveals that gene therapy might be the key to providing a permanent solution to HIV. By manipulating a specific molecule, researchers aim to induce long-term dormancy in the virus, offering hope for millions living with HIV. Discover how this innovative approach could change the landscape of HIV treatment.

Key Takeaways

  • Gene therapy may allow for permanent dormancy of HIV.
  • Research focuses on enhancing antisense transcript (AST) production.
  • Current treatments require lifelong antiretroviral therapy.
  • Over 39 million people live with HIV globally.
  • The study offers hope for reducing the burden of HIV treatment.

New Delhi, June 26 (NationPress) Gene therapy could be a pivotal method for permanently silencing HIV, offering a lasting and durable treatment against the virus responsible for AIDS, as per a recent study.

Researchers at Johns Hopkins University in the United States have discovered that a specific molecule within HIV can be manipulated and enhanced to induce long-term dormancy in the virus, a condition where HIV ceases to replicate.

This new research contributes to the expanding evidence which may assist scientists in creating a gene therapy that enhances the production of an “antisense transcript” (AST), according to Fabio Romerio, Associate Professor of molecular and comparative pathobiology at the Johns Hopkins University School of Medicine.

The study builds upon earlier findings indicating that AST is produced by HIV's genetic material and is a crucial part of a molecular pathway that effectively places the virus into dormancy, a state referred to as viral latency.

According to the World Health Organization, there are approximately 39.9 million individuals living with HIV globally, with 630,000 deaths attributed to HIV-related illnesses each year.

The conventional treatment for HIV requires patients to take daily antiretroviral therapy, which prevents the virus from replicating and spreading. This medication must be taken indefinitely and comes with various short- and long-term side effects. In contrast, gene therapy could necessitate as little as a single dose.

Even after years of antiretroviral therapy, the virus can persist in cells and tissues throughout the body, rapidly spreading if the patient discontinues treatment, Romerio stated.

“Our objective is to discover a method to provide a lasting and durable treatment for HIV,” remarked Rui Li, a postdoctoral fellow in Romerio’s lab and the lead author of the paper published in the journal Science Advances.

Romerio highlighted that these new insights could pave the way for gene therapies that permanently enhance AST production in T cells of HIV-positive individuals, effectively putting the virus in a state of long-term dormancy.

To explore the role of AST in viral dormancy, scientists initially examined a human cell line of CD4+ T cells, the immune cells targeted by HIV to insert its genome and replicate.

The team genetically modified these T cells, which had been infected with HIV, to increase AST production by inserting a genetic element capable of generating multiple AST copies.

The researchers also investigated AST in CD4+ T immune cells obtained with consent from 15 HIV-positive individuals.

Employing a method to accurately assess whether HIV is dormant or active, the scientists discovered that the virus remained inactive in all cells for four days, after which the AST-expressing DNA degraded within the T cells.

Point of View

I believe this research holds significant promise for the future of HIV treatment. The innovative approach of utilizing gene therapy to possibly induce long-term dormancy in the virus could revolutionize how we manage HIV, providing hope to millions. As we continue to report on advancements in medical science, ensuring that these breakthroughs are accessible and understandable to the public is essential.
NationPress
26/06/2025

Frequently Asked Questions

What is gene therapy?
Gene therapy is a medical technique that modifies a person's genes to treat or prevent disease. In the context of HIV, it aims to manipulate the virus's genetic material to induce dormancy.
How does the study propose to treat HIV?
The study suggests that by enhancing the production of an 'antisense transcript' (AST), researchers may force HIV into a state of long-term dormancy where it does not replicate.
What are the benefits of gene therapy over traditional treatments?
Unlike traditional antiretroviral therapies that require lifelong daily medication, gene therapy could potentially be administered in a single dose, reducing long-term side effects.
How prevalent is HIV worldwide?
Currently, approximately 39.9 million people are living with HIV, with around 630,000 annual deaths attributed to HIV-related illnesses, according to the World Health Organization.
What does viral latency mean?
Viral latency refers to a state in which the virus remains in the body without replicating, allowing it to evade the immune system while not causing immediate harm.