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T cell derived HIV-1 is present in the CSF in the face of suppressive antiretroviral therapy.

Authors :
Lustig G
Cele S
Karim F
Derache A
Ngoepe A
Khan K
Gosnell BI
Moosa MS
Ntshuba N
Marais S
Jeena PM
Govender K
Adamson J
Kløverpris H
Gupta RK
Harrichandparsad R
Patel VB
Sigal A
Source :
PLoS pathogens [PLoS Pathog] 2021 Sep 23; Vol. 17 (9), pp. e1009871. Date of Electronic Publication: 2021 Sep 23 (Print Publication: 2021).
Publication Year :
2021

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.<br />Competing Interests: The authors have declared that no competing interests exist. Author Ntombi Ntshuba was unable to confirm their authorship contributions. On their behalf, the corresponding author has reported their contributions to the best of their knowledge.

Details

Language :
English
ISSN :
1553-7374
Volume :
17
Issue :
9
Database :
MEDLINE
Journal :
PLoS pathogens
Publication Type :
Academic Journal
Accession number :
34555123
Full Text :
https://doi.org/10.1371/journal.ppat.1009871