T cell derived HIV-1 is present in the CSF in the face of suppressive antiretroviral therapy.
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Authors
Derache, Anne
Ngoepe, Abigail
Khan, Khadija
Gosnell, Bernadett I
Ntshuba, Ntombi
Marais, Suzaan
Jeena, Prakash M
Adamson, John
Kløverpris, Henrik
Patel, Vinod B
Publication Date
2021-09Journal Title
PLoS Pathog
ISSN
1553-7366
Publisher
Public Library of Science (PLoS)
Volume
17
Issue
9
Pages
e1009871
Language
eng
Type
Article
This Version
VoR
Physical Medium
Electronic-eCollection
Metadata
Show full item recordCitation
Lustig, G., Cele, S., Karim, F., Derache, A., Ngoepe, A., Khan, K., Gosnell, B. I., et al. (2021). T cell derived HIV-1 is present in the CSF in the face of suppressive antiretroviral therapy.. PLoS Pathog, 17 (9), e1009871. https://doi.org/10.1371/journal.ppat.1009871
Abstract
HIV cerebrospinal fluid (CSF) escape, where HIV is suppressed in blood but detectable in CSF, occurs when HIV persists in the CNS despite antiretroviral therapy (ART). To determine the virus producing cell type and whether lowered CSF ART levels are responsible for CSF escape, we collected blood and CSF from 156 neurosymptomatic participants from Durban, South Africa. We observed that 28% of participants with an undetectable HIV blood viral load showed CSF escape. We detected host cell surface markers on the HIV envelope to determine the cellular source of HIV in participants on the first line regimen of efavirenz, emtricitabine, and tenofovir. We confirmed CD26 as a marker which could differentiate between T cells and macrophages and microglia, and quantified CD26 levels on the virion surface, comparing the result to virus from in vitro infected T cells or macrophages. The measured CD26 level was consistent with the presence of T cell produced virus. We found no significant differences in ART concentrations between CSF escape and fully suppressed individuals in CSF or blood, and did not observe a clear association with drug resistance mutations in CSF virus which would allow HIV to replicate. Hence, CSF HIV in the face of ART may at least partly originate in CD4+ T cell populations.
Keywords
Adult, Alkynes, Anti-HIV Agents, Benzoxazines, Cyclopropanes, Emtricitabine, Female, HIV Infections, HIV-1, Humans, Male, Middle Aged, T-Lymphocytes, Tenofovir
Identifiers
External DOI: https://doi.org/10.1371/journal.ppat.1009871
This record's URL: https://www.repository.cam.ac.uk/handle/1810/330512
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