There are currently 38 million people living with HIV (PLWH) and due to current advances in combination antiretroviral therapy (cART), PLWH are living longer. However due to the latent viral reservoir, there is currently no cure for HIV as viral rebound arises following cART cessation. Therefore, a great effort has been put into defining this latent reservoir and strategies for eradication. One of these latent reservoirs is the brain, as demonstrated in both human and non-human primate models. Interestingly, brain latent reservoir can reseed peripheral organs following cART cessation. Understanding the role the brain plays in viral rebound and defining which cells contribute to CNS viral escape is critical for a viable cure strategy. Equally important is to define the neuroinflammatory signature under cART and changes following cART cessation to inform therapeutic strategies. In this application using a combinatorial imaging approach, we will define the viral reservoir in the brain after cART cessation in SIV-infected rhesus macaques (Aim 1) and using a multi-modal approach, we will define the neuroinflammatory signature in SIV-infected rhesus macaques following cART cessation (Aim 2). We will use brain tissue from 3 groups of SIV-infected rhesus macaques that are either cART nave, on cART or following cART cessation to address three fundamental questions: 1) Which cell type(s) contain rebounding virus following cART cessation in the CNS of SIV-infected rhesus macaques? 2) Do these cells containing rebounding virus following cART cessation have replication competent virus? And 3) What is the neuroinflammatory signature associated with viral rebound in the CNS following cART cessation? Collectively our studies will use state-of-the art imaging technologies to better understand the role of the brain as a viral reservoir to inform cure strategies that addresses the unique characteristics of this sanctuary site.

Public Health Relevance

Despite advances in drug therapy for controlling HIV infection, there is still no cure, because when people stop taking these anti-viral drugs, the virus comes back. Where the virus hides and what cells are responsible for viral rebound is under intense investigation. We will study the role of the brain in this phenomenon using state of the art imaging techniques in a well-controlled animal model.

Agency
National Institute of Health (NIH)
Institute
National Institute of Mental Health (NIMH)
Type
Exploratory/Developmental Grants (R21)
Project #
1R21MH125339-01
Application #
10125417
Study Section
Special Emphasis Panel (ZRG1)
Program Officer
Joseph, Jeymohan
Project Start
2020-09-01
Project End
2022-08-31
Budget Start
2020-09-01
Budget End
2021-08-31
Support Year
1
Fiscal Year
2020
Total Cost
Indirect Cost
Name
Rush University Medical Center
Department
Microbiology/Immun/Virology
Type
Schools of Medicine
DUNS #
068610245
City
Chicago
State
IL
Country
United States
Zip Code
60612