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Neurocognitive Impairment in HIV-Infected Naïve Patients with Advanced Disease: The Role of Virus and Intrathecal Immune Activation

Objective. To investigate intrathecal immune activation parameters and HIV-RNA in HIV-associated neurocognitive disorders (HAND) of advanced naïve HIV-infected patients and to evaluate their dynamics before and after initiation of antiretroviral therapy (ART). Methods. Cross-sectional and longitudin...

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Autores principales: Airoldi, Monica, Bandera, Alessandra, Trabattoni, Daria, Tagliabue, Benedetta, Arosio, Beatrice, Soria, Alessandro, Rainone, Veronica, Lapadula, Giuseppe, Annoni, Giorgio, Clerici, Mario, Gori, Andrea
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3320013/
https://www.ncbi.nlm.nih.gov/pubmed/22489249
http://dx.doi.org/10.1155/2012/467154
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author Airoldi, Monica
Bandera, Alessandra
Trabattoni, Daria
Tagliabue, Benedetta
Arosio, Beatrice
Soria, Alessandro
Rainone, Veronica
Lapadula, Giuseppe
Annoni, Giorgio
Clerici, Mario
Gori, Andrea
author_facet Airoldi, Monica
Bandera, Alessandra
Trabattoni, Daria
Tagliabue, Benedetta
Arosio, Beatrice
Soria, Alessandro
Rainone, Veronica
Lapadula, Giuseppe
Annoni, Giorgio
Clerici, Mario
Gori, Andrea
author_sort Airoldi, Monica
collection PubMed
description Objective. To investigate intrathecal immune activation parameters and HIV-RNA in HIV-associated neurocognitive disorders (HAND) of advanced naïve HIV-infected patients and to evaluate their dynamics before and after initiation of antiretroviral therapy (ART). Methods. Cross-sectional and longitudinal analysis of HIV RNA, proinflammatory cytokines (IL-6, IL-10, INF-γ, TNF-α, TGF-β1, and TGF-β2) and chemokines (MIP-1α, MIP-1β, and MCP-1) in plasma and cerebrospinal fluid (CSF) of HIV-infected patients with CD4 <200/μL. Results. HAND was diagnosed at baseline in 6/12 patients. Baseline CSF HIV-RNA was comparable in patients with or without HAND, whereas CSF concentration of IL-6 and MIP-1β, proinflammatory cytokines, was increased in HAND patients. CSF evaluation at 12 weeks was available in 10/12 cases. ART greatly reduced HIV-RNA in all patients. Nevertheless, IL-6 and MIP-1β remained elevated after 12 weeks of therapy in HAND patients, in whom CSF HIV RNA decay was slower than the plasmatic one as well. Conclusion. Immune activation, as indicated by inflammatory cytokines, but not higher levels of HIV-RNA is observed in advanced naïve HIV-infected patients with HAND. In HAND patients, ART introduction resulted in a less rapid clearance of CSF viremia compared to plasma and no modifications of intratechal immune activation.
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spelling pubmed-33200132012-04-09 Neurocognitive Impairment in HIV-Infected Naïve Patients with Advanced Disease: The Role of Virus and Intrathecal Immune Activation Airoldi, Monica Bandera, Alessandra Trabattoni, Daria Tagliabue, Benedetta Arosio, Beatrice Soria, Alessandro Rainone, Veronica Lapadula, Giuseppe Annoni, Giorgio Clerici, Mario Gori, Andrea Clin Dev Immunol Clinical Study Objective. To investigate intrathecal immune activation parameters and HIV-RNA in HIV-associated neurocognitive disorders (HAND) of advanced naïve HIV-infected patients and to evaluate their dynamics before and after initiation of antiretroviral therapy (ART). Methods. Cross-sectional and longitudinal analysis of HIV RNA, proinflammatory cytokines (IL-6, IL-10, INF-γ, TNF-α, TGF-β1, and TGF-β2) and chemokines (MIP-1α, MIP-1β, and MCP-1) in plasma and cerebrospinal fluid (CSF) of HIV-infected patients with CD4 <200/μL. Results. HAND was diagnosed at baseline in 6/12 patients. Baseline CSF HIV-RNA was comparable in patients with or without HAND, whereas CSF concentration of IL-6 and MIP-1β, proinflammatory cytokines, was increased in HAND patients. CSF evaluation at 12 weeks was available in 10/12 cases. ART greatly reduced HIV-RNA in all patients. Nevertheless, IL-6 and MIP-1β remained elevated after 12 weeks of therapy in HAND patients, in whom CSF HIV RNA decay was slower than the plasmatic one as well. Conclusion. Immune activation, as indicated by inflammatory cytokines, but not higher levels of HIV-RNA is observed in advanced naïve HIV-infected patients with HAND. In HAND patients, ART introduction resulted in a less rapid clearance of CSF viremia compared to plasma and no modifications of intratechal immune activation. Hindawi Publishing Corporation 2012 2012-03-27 /pmc/articles/PMC3320013/ /pubmed/22489249 http://dx.doi.org/10.1155/2012/467154 Text en Copyright © 2012 Monica Airoldi et al. https://creativecommons.org/licenses/by/3.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Clinical Study
Airoldi, Monica
Bandera, Alessandra
Trabattoni, Daria
Tagliabue, Benedetta
Arosio, Beatrice
Soria, Alessandro
Rainone, Veronica
Lapadula, Giuseppe
Annoni, Giorgio
Clerici, Mario
Gori, Andrea
Neurocognitive Impairment in HIV-Infected Naïve Patients with Advanced Disease: The Role of Virus and Intrathecal Immune Activation
title Neurocognitive Impairment in HIV-Infected Naïve Patients with Advanced Disease: The Role of Virus and Intrathecal Immune Activation
title_full Neurocognitive Impairment in HIV-Infected Naïve Patients with Advanced Disease: The Role of Virus and Intrathecal Immune Activation
title_fullStr Neurocognitive Impairment in HIV-Infected Naïve Patients with Advanced Disease: The Role of Virus and Intrathecal Immune Activation
title_full_unstemmed Neurocognitive Impairment in HIV-Infected Naïve Patients with Advanced Disease: The Role of Virus and Intrathecal Immune Activation
title_short Neurocognitive Impairment in HIV-Infected Naïve Patients with Advanced Disease: The Role of Virus and Intrathecal Immune Activation
title_sort neurocognitive impairment in hiv-infected naïve patients with advanced disease: the role of virus and intrathecal immune activation
topic Clinical Study
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3320013/
https://www.ncbi.nlm.nih.gov/pubmed/22489249
http://dx.doi.org/10.1155/2012/467154
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