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Arginase Activity in the Blood of Patients with Visceral Leishmaniasis and HIV Infection
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نویسنده
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takele y. ,abebe t. ,weldegebreal t. ,hailu a. ,hailu w. ,hurissa z. ,ali j. ,diro e. ,sisay y. ,cloke t. ,modolell m. ,munder m. ,tacchini-cottier f. ,müller i. ,kropf p.
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منبع
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plos neglected tropical diseases - 2013 - دوره : 7 - شماره : 1
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چکیده
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Background: visceral leishmaniasis is a parasitic disease associated with high mortality. the most important foci of visceral leishmaniasis in ethiopia are in the northwest and are predominantly associated with high rates of hiv co-infection. co-infection of visceral leishmaniasis patients with hiv results in higher mortality,treatment failure and relapse. we have previously shown that arginase,an enzyme associated with immunosuppression,was increased in patients with visceral leishmaniasis and in hiv seropositive patients; further our results showed that high arginase activity is a marker of disease severity. here,we tested the hypothesis that increased arginase activities associated with visceral leishmaniasis and hiv infections synergize in patients co-infected with both pathogens. methodology/principal findings: we recruited a cohort of patients with visceral leishmaniasis and a cohort of patients with visceral leishmaniasis and hiv infection from gondar,northwest ethiopia,and recorded and compared their clinical data. further,we measured the levels of arginase activity in the blood of these patients and identified the phenotype of arginase-expressing cells. our results show that cd4+ t cell counts were significantly lower and the parasite load in the spleen was significantly higher in co-infected patients. moreover,our results demonstrate that arginase activity was significantly higher in peripheral blood mononuclear cells and plasma of co-infected patients. finally,we identified the cells-expressing arginase in the pbmcs as low-density granulocytes. conclusion: our results suggest that increased arginase might contribute to the poor disease outcome characteristic of patients with visceral leishmaniasis and hiv co-infection. © 2013 takele et al.
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آدرس
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gondar university leishmaniasis research and treatment centre,university of gondar,gondar, Ethiopia, department of microbiology,immunology,parasitology and pathology,addis ababa university,addis ababa, Ethiopia, gondar university leishmaniasis research and treatment centre,university of gondar,gondar, Ethiopia, department of microbiology,immunology,parasitology and pathology,addis ababa university,addis ababa, Ethiopia, college of medicine and health sciences,university of gondar,gondar, Ethiopia, gondar university leishmaniasis research and treatment centre,university of gondar,gondar, Ethiopia, department of microbiology,immunology and parasitology,school of biomedical and laboratory sciences,university of gondar,gondar, Ethiopia, gondar university leishmaniasis research and treatment centre,university of gondar,gondar, Ethiopia, college of medicine and health sciences,university of gondar,gondar, Ethiopia, department of medicine,section of immunology,imperial college london,london, United Kingdom, department of cellular immunology,max-planck-institute for immunobiology and epigenetics,freiburg, Germany, third department of medicine (hematology,oncology,and pneumology),university medical center mainz,mainz, Germany, department of biochemistry,who immunology research and training center,university of lausanne,lausanne, Switzerland, department of medicine,section of immunology,imperial college london,london, United Kingdom, department of immunology and infection,london school of hygiene and tropical medicine,london, United Kingdom
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Authors
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