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Cerebrospinal fluid signs of neuronal damage after antiretroviral treatment interruption in HIV-1 infection

BACKGROUND: The neurofilament is a major structural component of myelinated axons. Increased cerebrospinal fluid (CSF) concentrations of the light chain of the neurofilament protein (NFL) can serve as a sensitive indicator of central nervous system (CNS) injury. To assess whether interrupting antire...

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Autores principales: Gisslén, Magnus, Rosengren, Lars, Hagberg, Lars, Deeks, Steven G, Price, Richard W
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2005
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1198215/
https://www.ncbi.nlm.nih.gov/pubmed/16109178
http://dx.doi.org/10.1186/1742-6405-2-6
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author Gisslén, Magnus
Rosengren, Lars
Hagberg, Lars
Deeks, Steven G
Price, Richard W
author_facet Gisslén, Magnus
Rosengren, Lars
Hagberg, Lars
Deeks, Steven G
Price, Richard W
author_sort Gisslén, Magnus
collection PubMed
description BACKGROUND: The neurofilament is a major structural component of myelinated axons. Increased cerebrospinal fluid (CSF) concentrations of the light chain of the neurofilament protein (NFL) can serve as a sensitive indicator of central nervous system (CNS) injury. To assess whether interrupting antiretroviral treatment of HIV infection might have a deleterious effect on the CNS, we measured NFL levels in HIV-infected subjects interrupting therapy. We identified subjects who had CSF HIV RNA concentrations below 50 copies/mL at the time combination antiretroviral therapy was interrupted, and for whom CSF samples were available before and after the interruption. RESULTS: A total of 8 subjects were studied. The median (range) CSF NFL level at baseline was <125 (<125–220) ng/L (normal <250 ng/L). All 8 subjects exhibited an increase in CSF and plasma HIV RNA after stopping therapy, accompanied by intrathecal immunoactivation as evidenced by CSF lymphocytic pleocytosis (7/8 patients) and increased CSF neopterin concentration (5/6 patients). Three subjects showed a consistent increase in CSF NFL, rising from <125 ng/L to a maximum of 880 (at day 148), 1,010 (day 58) and 10,930 ng/L (day 101). None exhibited new neurological symptoms or signs, or experienced functional deterioration during the period off treatment; of 5 who underwent brief quantitative neurological testing, none showed worsening performance. CONCLUSION: These findings suggest that resurgence of active HIV replication may result in measurable, albeit subclinical, CNS injury. Further studies are needed to define the frequency and pathobiological importance of the increase in CSF NFL.
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spelling pubmed-11982152005-09-03 Cerebrospinal fluid signs of neuronal damage after antiretroviral treatment interruption in HIV-1 infection Gisslén, Magnus Rosengren, Lars Hagberg, Lars Deeks, Steven G Price, Richard W AIDS Res Ther Research BACKGROUND: The neurofilament is a major structural component of myelinated axons. Increased cerebrospinal fluid (CSF) concentrations of the light chain of the neurofilament protein (NFL) can serve as a sensitive indicator of central nervous system (CNS) injury. To assess whether interrupting antiretroviral treatment of HIV infection might have a deleterious effect on the CNS, we measured NFL levels in HIV-infected subjects interrupting therapy. We identified subjects who had CSF HIV RNA concentrations below 50 copies/mL at the time combination antiretroviral therapy was interrupted, and for whom CSF samples were available before and after the interruption. RESULTS: A total of 8 subjects were studied. The median (range) CSF NFL level at baseline was <125 (<125–220) ng/L (normal <250 ng/L). All 8 subjects exhibited an increase in CSF and plasma HIV RNA after stopping therapy, accompanied by intrathecal immunoactivation as evidenced by CSF lymphocytic pleocytosis (7/8 patients) and increased CSF neopterin concentration (5/6 patients). Three subjects showed a consistent increase in CSF NFL, rising from <125 ng/L to a maximum of 880 (at day 148), 1,010 (day 58) and 10,930 ng/L (day 101). None exhibited new neurological symptoms or signs, or experienced functional deterioration during the period off treatment; of 5 who underwent brief quantitative neurological testing, none showed worsening performance. CONCLUSION: These findings suggest that resurgence of active HIV replication may result in measurable, albeit subclinical, CNS injury. Further studies are needed to define the frequency and pathobiological importance of the increase in CSF NFL. BioMed Central 2005-08-18 /pmc/articles/PMC1198215/ /pubmed/16109178 http://dx.doi.org/10.1186/1742-6405-2-6 Text en Copyright © 2005 Gisslén et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License ( (http://creativecommons.org/licenses/by/2.0) ), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research
Gisslén, Magnus
Rosengren, Lars
Hagberg, Lars
Deeks, Steven G
Price, Richard W
Cerebrospinal fluid signs of neuronal damage after antiretroviral treatment interruption in HIV-1 infection
title Cerebrospinal fluid signs of neuronal damage after antiretroviral treatment interruption in HIV-1 infection
title_full Cerebrospinal fluid signs of neuronal damage after antiretroviral treatment interruption in HIV-1 infection
title_fullStr Cerebrospinal fluid signs of neuronal damage after antiretroviral treatment interruption in HIV-1 infection
title_full_unstemmed Cerebrospinal fluid signs of neuronal damage after antiretroviral treatment interruption in HIV-1 infection
title_short Cerebrospinal fluid signs of neuronal damage after antiretroviral treatment interruption in HIV-1 infection
title_sort cerebrospinal fluid signs of neuronal damage after antiretroviral treatment interruption in hiv-1 infection
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1198215/
https://www.ncbi.nlm.nih.gov/pubmed/16109178
http://dx.doi.org/10.1186/1742-6405-2-6
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