Gene expression and chromatin conformation of microglia in virally suppressed people with HIV

Author:

Schlachetzki Johannes CM12ORCID,Gianella Sara3,Ouyang Zhengyu1,Lana Addison J1,Yang Xiaoxu4,O’Brien Sydney1,Challacombe Jean F1,Gaskill Peter J5ORCID,Jordan-Sciutto Kelly L6ORCID,Chaillon Antoine3,Moore David7,Achim Cristian L8,Ellis Ronald J2ORCID,Smith Davey M3ORCID,Glass Christopher K1ORCID

Affiliation:

1. Department of Cellular and Molecular Medicine, University of California San Diego

2. Department of Neurosciences, University of California San Diego

3. Department of Medicine, Division of Infectious Diseases and Global Public Health, University of California San Diego

4. Department of Human Genetics, University of Utah, Salt Lake City, UT, USA

5. Department of Pharmacology and Physiology, Drexel University College of Medicine, Philadelphia, PA, USA

6. Department of Oral Medicine, School of Dental Medicine, University of Pennsylvania, Philadelphia, PA, USA

7. Department of Psychiatry, University of California San Diego

8. Department of Pathology, University of California San Diego

Abstract

The presence of HIV in sequestered reservoirs is a central impediment to a functional cure, allowing HIV to persist despite life-long antiretroviral therapy (ART), and driving a variety of comorbid conditions. Our understanding of the latent HIV reservoir in the central nervous system is incomplete, because of difficulties in accessing human central nervous system tissues. Microglia contribute to HIV reservoirs, but the molecular phenotype of HIV-infected microglia is poorly understood. We leveraged the unique “Last Gift” rapid autopsy program, in which people with HIV are closely followed until days or even hours before death. Microglial populations were heterogeneous regarding their gene expression profiles but showed similar chromatin accessibility landscapes. Despite ART, we detected occasional microglia containing cell-associated HIV RNA and HIV DNA integrated into open regions of the host’s genome (∼0.005%). Microglia with detectable HIV RNA showed an inflammatory phenotype. These results demonstrate a distinct myeloid cell reservoir in the brains of people with HIV despite suppressive ART. Strategies for curing HIV and neurocognitive impairment will need to consider the myeloid compartment to be successful.

Funder

NIH

San Diego Center for AIDS Research

California NeuroAIDS Tissue Network

Publisher

Life Science Alliance, LLC

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