Immune Response in the Central Nervous system Are Anatomically Segregated in a Non-Human Primate Model of Human Immunodeficiency Virus Infection
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Published version
Author(s)
Type
Journal Article
Abstract
The human immunodeficiency virus (HIV) accesses the central nervous system (CNS) early during infection, leading to HIV-associated cognitive impairment and establishment of a viral reservoir. Here, we describe a dichotomy in inflammatory responses in different CNS regions in simian immunodeficiency virus (SIV)-infected macaques, a model for HIV infection. We found increased expression of inflammatory genes and perivascular leukocyte infiltration in the midbrain of SIV-infected macaques. Conversely, the frontal lobe showed downregulation of inflammatory genes associated with interferon-γ and interleukin-6 pathways, and absence of perivascular cuffing. These immunologic alterations were not accompanied by differences in SIV transcriptional activity within the tissue. Altered expression of genes associated with neurotoxicity was observed in both midbrain and frontal lobe. The segregation of inflammatory responses to specific regions of the CNS may both account for HIV-associated neurological symptoms and constitute a critical hurdle for HIV eradication by shielding the CNS viral reservoir from antiviral immunity.
Date Issued
2017-03-30
Date Acceptance
2017-03-14
Citation
Frontiers in Immunology, 2017, 8
ISSN
1664-3224
Publisher
Frontiers Media
Journal / Book Title
Frontiers in Immunology
Volume
8
Copyright Statement
© 2017 Tavano, Tsipouri, Hardy, Royle, Keegan, Fuchs, Patterson, Almond,
Berry, Ham, Ferguson and Boasso. This is an open-access article distributed under the
terms of the Creative Commons Attribution License (CC BY https://creativecommons.org/licenses/by/4.0/). The use, distribution or
reproduction in other forums is permitted, provided the original author(s) or licensor
are credited and that the original publication in this journal is cited, in accordance
with accepted academic practice. No use, distribution or reproduction is permitted
which does not comply with these terms.
Berry, Ham, Ferguson and Boasso. This is an open-access article distributed under the
terms of the Creative Commons Attribution License (CC BY https://creativecommons.org/licenses/by/4.0/). The use, distribution or
reproduction in other forums is permitted, provided the original author(s) or licensor
are credited and that the original publication in this journal is cited, in accordance
with accepted academic practice. No use, distribution or reproduction is permitted
which does not comply with these terms.
Sponsor
Bill & Melinda Gates Foundation
Identifier
http://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcApp=PARTNER_APP&SrcAuth=LinksAMR&KeyUT=WOS:000397635300001&DestLinkType=FullRecord&DestApp=ALL_WOS&UsrCustomerID=1ba7043ffcc86c417c072aa74d649202
Grant Number
38639
Subjects
Science & Technology
Life Sciences & Biomedicine
Immunology
simian immunodeficiency virus
central nervous system
neuroinflammation
neurotoxicity
indoleamine (2,3)-dioxygenase
ENHANCES MACROPHAGE TROPISM
NEUROCOGNITIVE DISORDERS
HIV-INFECTION
T-CELLS
CYNOMOLGUS MACAQUES
BRAIN INFECTION
SIV
DEMENTIA
CNS
SIVMAC251
Publication Status
Published
Article Number
ARTN 361