Blood-brain barrier and retroviral infections

Homeostasis in the central nervous system (CNS) is maintained by active interfaces between the bloodstream and the brain parenchyma. The blood-brain barrier (BBB) constitutes a selective filter for exchange of water, solutes, nutrients, and controls toxic compounds or pathogens entry. Some parasites...

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Main Authors: Miller, Florence, Afonso, Philippe V., Gessain, Antoine, Ceccaldi, Pierre-Emmanuel
Format: Online
Language:English
Published: Landes Bioscience 2012
Online Access:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3396701/
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spelling pubmed-33967012012-07-16 Blood-brain barrier and retroviral infections Miller, Florence Afonso, Philippe V. Gessain, Antoine Ceccaldi, Pierre-Emmanuel Review Homeostasis in the central nervous system (CNS) is maintained by active interfaces between the bloodstream and the brain parenchyma. The blood-brain barrier (BBB) constitutes a selective filter for exchange of water, solutes, nutrients, and controls toxic compounds or pathogens entry. Some parasites, bacteria, and viruses have however developed various CNS invasion strategies, and can bypass the brain barriers. Concerning viruses, these strategies include transport along neural pathways, transcytosis, infection of the brain endothelial cells, breaching of the BBB, and passage of infected-leukocytes. Moreover, neurotropic viruses can alter BBB functions, thus compromising CNS homeostasis. Retroviruses have been associated to human neurological diseases: HIV (human immunodeficiency virus 1) can induce HIV-associated dementia, and HTLV-1 (human T lymphotropic virus 1) is the etiological factor of tropical spastic paraparesis/HTLV-1 associated myelopathy (TSP/HAM). The present review focuses on how the different retroviruses interact with this structure, bypass it and alter its functions. Landes Bioscience 2012-03-01 /pmc/articles/PMC3396701/ /pubmed/22460635 http://dx.doi.org/10.4161/viru.19697 Text en Copyright © 2012 Landes Bioscience http://creativecommons.org/licenses/by-nc/3.0/ This is an open-access article licensed under a Creative Commons Attribution-NonCommercial 3.0 Unported License. The article may be redistributed, reproduced, and reused for non-commercial purposes, provided the original source is properly cited.
repository_type Open Access Journal
institution_category Foreign Institution
institution US National Center for Biotechnology Information
building NCBI PubMed
collection Online Access
language English
format Online
author Miller, Florence
Afonso, Philippe V.
Gessain, Antoine
Ceccaldi, Pierre-Emmanuel
spellingShingle Miller, Florence
Afonso, Philippe V.
Gessain, Antoine
Ceccaldi, Pierre-Emmanuel
Blood-brain barrier and retroviral infections
author_facet Miller, Florence
Afonso, Philippe V.
Gessain, Antoine
Ceccaldi, Pierre-Emmanuel
author_sort Miller, Florence
title Blood-brain barrier and retroviral infections
title_short Blood-brain barrier and retroviral infections
title_full Blood-brain barrier and retroviral infections
title_fullStr Blood-brain barrier and retroviral infections
title_full_unstemmed Blood-brain barrier and retroviral infections
title_sort blood-brain barrier and retroviral infections
description Homeostasis in the central nervous system (CNS) is maintained by active interfaces between the bloodstream and the brain parenchyma. The blood-brain barrier (BBB) constitutes a selective filter for exchange of water, solutes, nutrients, and controls toxic compounds or pathogens entry. Some parasites, bacteria, and viruses have however developed various CNS invasion strategies, and can bypass the brain barriers. Concerning viruses, these strategies include transport along neural pathways, transcytosis, infection of the brain endothelial cells, breaching of the BBB, and passage of infected-leukocytes. Moreover, neurotropic viruses can alter BBB functions, thus compromising CNS homeostasis. Retroviruses have been associated to human neurological diseases: HIV (human immunodeficiency virus 1) can induce HIV-associated dementia, and HTLV-1 (human T lymphotropic virus 1) is the etiological factor of tropical spastic paraparesis/HTLV-1 associated myelopathy (TSP/HAM). The present review focuses on how the different retroviruses interact with this structure, bypass it and alter its functions.
publisher Landes Bioscience
publishDate 2012
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3396701/
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