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Increased Level of Arginase Activity Correlates with Disease Severity in HIV‐Seropositive Patients
Author(s) -
Tom Cloke,
Lucy Garvey,
BeakSan Choi,
Tamrat Abebe,
A. Hailu,
Maggie Hancock,
Ulrich D. Kadolsky,
Charles R. M. Bangham,
Markus Munder,
Ingrid Müller,
Graham P. Taylor,
Pascale Kropf
Publication year - 2010
Publication title -
the journal of infectious diseases
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.69
H-Index - 252
eISSN - 1537-6613
pISSN - 0022-1899
DOI - 10.1086/653736
Subject(s) - arginase , peripheral blood mononuclear cell , immune system , immunology , immunosuppression , viral load , immunopathology , virus , medicine , lentivirus , viral disease , biology , arginine , biochemistry , amino acid , in vitro
Infection with human immunodeficiency virus (HIV) results in a chronic infection that progressively impairs the immune system. Although depletion of CD4(+) T cells is frequently used to explain immunosuppression, chronicity of infection and progressive loss of CD4(+) T cells are not sufficient to fully account for immune dysregulation. Arginase-induced l-arginine deprivation is emerging as a key mechanism for the down-regulation of immune responses. Here, we hypothesized that the level of arginase activity increases with disease severity in HIV-seropositive patients. We determined the levels of arginase activity in peripheral blood mononuclear cells from HIV-seropositive patients and uninfected control participants. Our results show that peripheral blood mononuclear cells from HIV-seropositive patients with low CD4(+) T cell counts expressed statistically significantly higher levels of arginase activity, compared with patients with high CD4(+) T cell counts or uninfected control participants. Furthermore, we found a statistically significant correlation between high level of arginase activity and high viral load in HIV-seropositive patients.

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