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Antiretroviral therapy abrogates association between arginase activity and HIV disease severity()

Arginase-induced L-arginine deprivation is emerging as a key mechanism for the downregulation of immune responses. We hypothesised that arginase activity increases with disease severity in HIV-seropositive patients. Our results show that peripheral blood mononuclear cells (PBMCs) from 23 HIV-seropos...

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Autores principales: Cloke, T.E., Abebe, T., Hailu, A., Munder, M., Taylor, G.P., Müller, I., Kropf, P.
Formato: Texto
Lenguaje:English
Publicado: Oxford University Press 2010
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2977531/
https://www.ncbi.nlm.nih.gov/pubmed/20843532
http://dx.doi.org/10.1016/j.trstmh.2010.08.004
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author Cloke, T.E.
Abebe, T.
Hailu, A.
Munder, M.
Taylor, G.P.
Müller, I.
Kropf, P.
author_facet Cloke, T.E.
Abebe, T.
Hailu, A.
Munder, M.
Taylor, G.P.
Müller, I.
Kropf, P.
author_sort Cloke, T.E.
collection PubMed
description Arginase-induced L-arginine deprivation is emerging as a key mechanism for the downregulation of immune responses. We hypothesised that arginase activity increases with disease severity in HIV-seropositive patients. Our results show that peripheral blood mononuclear cells (PBMCs) from 23 HIV-seropositive patients with low CD4(+) T cell counts (≤350 cells/μl) expressed significantly more arginase compared with 21 patients with high CD4(+) T cell counts. Furthermore, we found a significant association between the two principal prognostic markers used to monitor HIV disease (CD4(+) T cell count and plasma viral load) and PBMC arginase activity in antiretroviral therapy naïve patients but not in patients undergoing therapy.
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spelling pubmed-29775312010-12-07 Antiretroviral therapy abrogates association between arginase activity and HIV disease severity() Cloke, T.E. Abebe, T. Hailu, A. Munder, M. Taylor, G.P. Müller, I. Kropf, P. Trans R Soc Trop Med Hyg Society Meeting Paper Arginase-induced L-arginine deprivation is emerging as a key mechanism for the downregulation of immune responses. We hypothesised that arginase activity increases with disease severity in HIV-seropositive patients. Our results show that peripheral blood mononuclear cells (PBMCs) from 23 HIV-seropositive patients with low CD4(+) T cell counts (≤350 cells/μl) expressed significantly more arginase compared with 21 patients with high CD4(+) T cell counts. Furthermore, we found a significant association between the two principal prognostic markers used to monitor HIV disease (CD4(+) T cell count and plasma viral load) and PBMC arginase activity in antiretroviral therapy naïve patients but not in patients undergoing therapy. Oxford University Press 2010-11 /pmc/articles/PMC2977531/ /pubmed/20843532 http://dx.doi.org/10.1016/j.trstmh.2010.08.004 Text en © 2010 Elsevier Ltd. https://creativecommons.org/licenses/by/4.0/This work is licensed under a Creative Commons Attribution 4.0 International License (https://creativecommons.org/licenses/by/4.0/) , which allows reusers to distribute, remix, adapt, and build upon the material in any medium or format, so long as attribution is given to the creator. The license allows for commercial use.
spellingShingle Society Meeting Paper
Cloke, T.E.
Abebe, T.
Hailu, A.
Munder, M.
Taylor, G.P.
Müller, I.
Kropf, P.
Antiretroviral therapy abrogates association between arginase activity and HIV disease severity()
title Antiretroviral therapy abrogates association between arginase activity and HIV disease severity()
title_full Antiretroviral therapy abrogates association between arginase activity and HIV disease severity()
title_fullStr Antiretroviral therapy abrogates association between arginase activity and HIV disease severity()
title_full_unstemmed Antiretroviral therapy abrogates association between arginase activity and HIV disease severity()
title_short Antiretroviral therapy abrogates association between arginase activity and HIV disease severity()
title_sort antiretroviral therapy abrogates association between arginase activity and hiv disease severity()
topic Society Meeting Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2977531/
https://www.ncbi.nlm.nih.gov/pubmed/20843532
http://dx.doi.org/10.1016/j.trstmh.2010.08.004
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