Cerebrospinal fluid CD4+ T cell infection in humans and macaques during acute HIV-1 and SHIV infection.

HIV-1 replication within the central nervous system (CNS) impairs neurocognitive function and has the potential to establish persistent, compartmentalized viral reservoirs. The origins of HIV-1 detected in the CNS compartment are unknown, including whether cells within the cerebrospinal fluid (CSF)...

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Main Authors: Vishakha Sharma, Matthew Creegan, Andrey Tokarev, Denise Hsu, Bonnie M Slike, Carlo Sacdalan, Phillip Chan, Serena Spudich, Jintanat Ananworanich, Michael A Eller, Shelly J Krebs, Sandhya Vasan, Diane L Bolton, RV254/SEARCH010 and RV304/SEARCH013 Study Teams
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2021-12-01
Series:PLoS Pathogens
Online Access:https://journals.plos.org/plospathogens/article/file?id=10.1371/journal.ppat.1010105&type=printable
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author Vishakha Sharma
Matthew Creegan
Andrey Tokarev
Denise Hsu
Bonnie M Slike
Carlo Sacdalan
Phillip Chan
Serena Spudich
Jintanat Ananworanich
Michael A Eller
Shelly J Krebs
Sandhya Vasan
Diane L Bolton
RV254/SEARCH010 and RV304/SEARCH013 Study Teams
author_facet Vishakha Sharma
Matthew Creegan
Andrey Tokarev
Denise Hsu
Bonnie M Slike
Carlo Sacdalan
Phillip Chan
Serena Spudich
Jintanat Ananworanich
Michael A Eller
Shelly J Krebs
Sandhya Vasan
Diane L Bolton
RV254/SEARCH010 and RV304/SEARCH013 Study Teams
author_sort Vishakha Sharma
collection DOAJ
description HIV-1 replication within the central nervous system (CNS) impairs neurocognitive function and has the potential to establish persistent, compartmentalized viral reservoirs. The origins of HIV-1 detected in the CNS compartment are unknown, including whether cells within the cerebrospinal fluid (CSF) produce virus. We measured viral RNA+ cells in CSF from acutely infected macaques longitudinally and people living with early stages of acute HIV-1. Active viral transcription (spliced viral RNA) was present in CSF CD4+ T cells as early as four weeks post-SHIV infection, and among all acute HIV-1 specimens (N = 6; Fiebig III/IV). Replication-inactive CD4+ T cell infection, indicated by unspliced viral RNA in the absence of spliced viral RNA, was even more prevalent, present in CSF of >50% macaques and human CSF at ~10-fold higher frequency than productive infection. Infection levels were similar between CSF and peripheral blood (and lymph nodes in macaques), indicating comparable T cell infection across these compartments. In addition, surface markers of activation were increased on CSF T cells and monocytes and correlated with CSF soluble markers of inflammation. These studies provide direct evidence of HIV-1 replication in CD4+ T cells and broad immune activation in peripheral blood and the CNS during acute infection, likely contributing to early neuroinflammation and reservoir seeding. Thus, early initiation of antiretroviral therapy may not be able to prevent establishment of CNS viral reservoirs and sources of long-term inflammation, important targets for HIV-1 cure and therapeutic strategies.
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spelling doaj-art-16b8b6926f974bd59d2620d0c8b1fc0a2025-08-20T02:22:26ZengPublic Library of Science (PLoS)PLoS Pathogens1553-73661553-73742021-12-011712e101010510.1371/journal.ppat.1010105Cerebrospinal fluid CD4+ T cell infection in humans and macaques during acute HIV-1 and SHIV infection.Vishakha SharmaMatthew CreeganAndrey TokarevDenise HsuBonnie M SlikeCarlo SacdalanPhillip ChanSerena SpudichJintanat AnanworanichMichael A EllerShelly J KrebsSandhya VasanDiane L BoltonRV254/SEARCH010 and RV304/SEARCH013 Study TeamsHIV-1 replication within the central nervous system (CNS) impairs neurocognitive function and has the potential to establish persistent, compartmentalized viral reservoirs. The origins of HIV-1 detected in the CNS compartment are unknown, including whether cells within the cerebrospinal fluid (CSF) produce virus. We measured viral RNA+ cells in CSF from acutely infected macaques longitudinally and people living with early stages of acute HIV-1. Active viral transcription (spliced viral RNA) was present in CSF CD4+ T cells as early as four weeks post-SHIV infection, and among all acute HIV-1 specimens (N = 6; Fiebig III/IV). Replication-inactive CD4+ T cell infection, indicated by unspliced viral RNA in the absence of spliced viral RNA, was even more prevalent, present in CSF of >50% macaques and human CSF at ~10-fold higher frequency than productive infection. Infection levels were similar between CSF and peripheral blood (and lymph nodes in macaques), indicating comparable T cell infection across these compartments. In addition, surface markers of activation were increased on CSF T cells and monocytes and correlated with CSF soluble markers of inflammation. These studies provide direct evidence of HIV-1 replication in CD4+ T cells and broad immune activation in peripheral blood and the CNS during acute infection, likely contributing to early neuroinflammation and reservoir seeding. Thus, early initiation of antiretroviral therapy may not be able to prevent establishment of CNS viral reservoirs and sources of long-term inflammation, important targets for HIV-1 cure and therapeutic strategies.https://journals.plos.org/plospathogens/article/file?id=10.1371/journal.ppat.1010105&type=printable
spellingShingle Vishakha Sharma
Matthew Creegan
Andrey Tokarev
Denise Hsu
Bonnie M Slike
Carlo Sacdalan
Phillip Chan
Serena Spudich
Jintanat Ananworanich
Michael A Eller
Shelly J Krebs
Sandhya Vasan
Diane L Bolton
RV254/SEARCH010 and RV304/SEARCH013 Study Teams
Cerebrospinal fluid CD4+ T cell infection in humans and macaques during acute HIV-1 and SHIV infection.
PLoS Pathogens
title Cerebrospinal fluid CD4+ T cell infection in humans and macaques during acute HIV-1 and SHIV infection.
title_full Cerebrospinal fluid CD4+ T cell infection in humans and macaques during acute HIV-1 and SHIV infection.
title_fullStr Cerebrospinal fluid CD4+ T cell infection in humans and macaques during acute HIV-1 and SHIV infection.
title_full_unstemmed Cerebrospinal fluid CD4+ T cell infection in humans and macaques during acute HIV-1 and SHIV infection.
title_short Cerebrospinal fluid CD4+ T cell infection in humans and macaques during acute HIV-1 and SHIV infection.
title_sort cerebrospinal fluid cd4 t cell infection in humans and macaques during acute hiv 1 and shiv infection
url https://journals.plos.org/plospathogens/article/file?id=10.1371/journal.ppat.1010105&type=printable
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