Related Experiment Video
Updated: Jul 6, 2025

06:07
Oral Combinational Antiretroviral Treatment in HIV-1 Infected Humanized Mice
Published on: October 6, 2022
2.4K
Advancements in Cell-Based Therapies for HIV Cure
1Gladstone Institute of Virology, Gladstone Institutes, 1650 Owens St., San Francisco, CA 941578, USA.
Cells
|January 11, 2024
Summary
Cellular therapies like CAR-T cells offer new hope for an acquired immunodeficiency syndrome (AIDS) cure. Research continues to address challenges in viral reservoir control and therapy stability for effective human immunodeficiency virus (HIV-1) treatment.
Area of Science:
- Immunology and Virology
- Cellular Therapy Research
Background:
- Combination antiretroviral therapy (ART) has significantly improved human immunodeficiency virus (HIV-1) management since the 1990s, suppressing viral replication and preventing acquired immunodeficiency syndrome (AIDS).
Purpose of the Study:
- To provide a consolidated overview of cell-based therapies for HIV-1, exploring strategies for a potential cure.
- To highlight the potential of CAR-T cell approaches, gene editing, and immune modulation in HIV-1 cure research.
Main Methods:
- Review and synthesis of current scientific literature on cellular therapies for HIV-1.
- Focus on chimeric antigen receptor T-cell (CAR-T) therapy, gene editing techniques, and immune modulation strategies.
Main Results:
- Cellular therapies show promise for addressing persistent challenges in HIV-1 cure research.
- Identified challenges include CAR-T cell susceptibility to HIV infection, therapy stability, and controlling the viral reservoir.
Conclusions:
- Continued research is essential to overcome existing hurdles in cellular therapy for HIV-1.
- Cellular therapies hold significant potential for advancing the pursuit of an HIV-1 cure.
Related Concept Videos
Retrovirus Life Cycles
46.0K
Retroviruses have a single-stranded RNA genome that undergoes a special form of replication. Once the retrovirus has entered the host cell, an enzyme called reverse transcriptase synthesizes double-stranded DNA from the retroviral RNA genome. This DNA copy of the genome is then integrated into the host’s genome inside the nucleus via an enzyme called integrase. Consequently, the retroviral genome is transcribed into RNA whenever the host’s genome is transcribed, allowing the...
46.0K
iPS Cell Differentiation
2.7K
The ability of induced pluripotent stem cells or iPSCs to differentiate into most body cell types has stimulated repair and regenerative medicine research over the past few decades. iPSC-derived blood cells, hepatocytes, beta islet cells, cardiomyocytes, neurons, and other cell types can repair injuries or regenerate damaged tissue in diseases such as diabetes and neurodegenerative disorders.
2.7K
Gene Therapy
25.4K
Gene therapy is a technique where a gene is inserted into a person’s cells to prevent or treat a serious disease. The added gene may be a healthy version of the gene that is mutated in the patient, or it could be a different gene that inactivates or compensates for the patient’s disease-causing gene. For example, in patients with severe combined immunodeficiency (SCID) due to a mutation in the gene for the enzyme adenosine deaminase, a functioning version of the gene can be...
25.4K

