Evaluation of Archival HIV DNA in Brain and Lymphoid Tissues.

TitleEvaluation of Archival HIV DNA in Brain and Lymphoid Tissues.
Publication TypeJournal Article
Year of Publication2023
AuthorsOliveira, MF, Pankow, A, Vollbrecht, T, Kumar, NM, Cabalero, G, Ignacio, C, Zhao, M, Vitomirov, A, Gouaux, B, Nakawawa, M, Murrell, B, Ellis, RJ, Gianella, S
JournalJ Virol
Volume97
Issue6
Paginatione0054323
Date Published2023 Jun 29
ISSN1098-5514
KeywordsBrain, DNA, Viral, env Gene Products, Human Immunodeficiency Virus, Female, HIV Infections, HIV-1, Humans, Lymphoid Tissue, Male, Middle Aged, Proviruses, Spleen
Abstract

HIV reservoirs persist in anatomic compartments despite antiretroviral therapy (ART). Characterizing archival HIV DNA in the central nervous system (CNS) and other tissues is crucial to inform cure strategies. We evaluated paired autopsy brain-frontal cortex (FC), occipital cortex (OCC), and basal ganglia (BG)-and peripheral lymphoid tissues from 63 people with HIV. Participants passed away while virally suppressed on ART at the last visit and without evidence of CNS opportunistic disease. We quantified total HIV DNA in all participants and obtained full-length HIV-envelope (FL HIV-) sequences from a subset of 14 participants. We detected HIV DNA () in most brain (65.1%) and all lymphoid tissues. Lymphoid tissues had higher HIV DNA levels than the brain ( < 0.01). Levels of HIV between BG and FC were similar ( > 0.2), while OCC had the lowest levels ( = 0.01). Females had higher HIV DNA levels in tissues than males (,  = 0.03; 2-LTR,  = 0.05), suggesting possible sex-associated mechanisms for HIV reservoir persistence. Most FL HIV- sequences ( = 143) were intact, while 42 were defective. Clonal sequences were found in 8 out of 14 participants, and 1 participant had clonal defective sequences in the brain and spleen, suggestive of cell migration. From 10 donors with paired brain and lymphoid sequences, we observed evidence of compartmentalized sequences in 2 donors. Our data further the idea that the brain is a site for archival HIV DNA during ART where compartmentalized provirus may occur in a subset of people. Future studies assessing FL HIV-provirus and replication competence are needed to further evaluate the HIV reservoirs in tissues. HIV infection of the brain is associated with adverse neuropsychiatric outcomes, despite efficient antiretroviral treatment. HIV may persist in reservoirs in the brain and other tissues, which can seed virus replication if treatment is interrupted, representing a major challenge to cure HIV. We evaluated reservoirs and genetic features in postmortem brain and lymphoid tissues from people with HIV who passed away during suppressed HIV replication. We found a differential distribution of HIV reservoirs across brain regions which was lower than that in lymphoid tissues. We observed that most HIV reservoirs in tissues had intact envelope sequences, suggesting they could potentially generate replicative viruses. We found that women had higher HIV reservoir levels in brain and lymphoid tissues than men, suggesting possible sex-based mechanisms of maintenance of HIV reservoirs in tissues, warranting further investigation. Characterizing the archival HIV DNA in tissues is important to inform future HIV cure strategies.

DOI10.1128/jvi.00543-23
Alternate JournalJ Virol
PubMed ID37184401
PubMed Central IDPMC10308944
Grant ListU24 MH100929 / MH / NIMH NIH HHS / United States
U24 MH100925 / MH / NIMH NIH HHS / United States
U24 MH100931 / MH / NIMH NIH HHS / United States
U24 MH100928 / MH / NIMH NIH HHS / United States
P30 DK063491 / DK / NIDDK NIH HHS / United States
P30 MH062512 / MH / NIMH NIH HHS / United States
P30 AI036214 / AI / NIAID NIH HHS / United States
U24 MH100930 / MH / NIMH NIH HHS / United States
R25 MH081482 / MH / NIMH NIH HHS / United States
R01 AG061066 / AG / NIA NIH HHS / United States
R01 AI147821 / AI / NIAID NIH HHS / United States
R21 HD094646 / HD / NICHD NIH HHS / United States
P30 DK120515 / DK / NIDDK NIH HHS / United States
P30 CA023100 / CA / NCI NIH HHS / United States
R21 AI134295 / AI / NIAID NIH HHS / United States