Date: February 29, 2024 By:
Ragon faculty Mathias Lichterfeld, MD, PhD, and Xu Yu, MD, have co-authored a paper published in Cell which found evidence that a combination of two drugs increases the vulnerability of HIV-1 reservoir cells to the immune system — which shows promising results in targeting and reducing the HIV-1 reservoir in people living with HIV.
Using samples provided by a Massachusetts General Hospital human clinical trial, the study found combined treatment with the histone deacetylase inhibitor panobinostat and pegylated interferon-a2a increased the immunological vulnerability of HIV-1 reservoir cells.
This treatment was found to transform the pool of HIV-1 reservoir cells by favoring certain types of HIV-1 proviruses over others. Specifically, the study found that the treatment led to an increase in HIV-1 proviruses integrated in specific genes and chromatin regions, while proviruses near certain molecular target sites were actively selected against. This suggests that the treatment can alter the composition of HIV-1 reservoir cells, potentially affecting the persistence of the virus.
Their findings, to be published in Cell next month, reveal how the virus manipulates immune system processes to avoid destruction by natural killer (NK) cells, a type of white blood cell that is crucial for fighting viral infections.
The lab of the Ragon Institute faculty member Hernandez Moura Silva, PhD, recently published a review in Science Immunology regarding resident tissue macrophages (RTMs), shedding light on their multifaceted roles in organ health.
After three years off due to the COVID-19 pandemic, the Ragon-MIT course HST.434 returned this January to provide 24 students a once in a lifetime learning experience