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HCV coinfection of the HIV-infected patients with discordant CD4+ T-cell response to antiretroviral therapy leads to intense systemic inflammation
Authors:K. V. Shmagel  L. B. Korolevskaya  E. V. Saidakova  N. G. Shmagel  V. A. Chereshnev  L. Margolis  D. Anthony  M. Lederman
Affiliation:1.Institute of Ecology and Genetics of Microorganisms, Ural Branch,Russian Academy of Sciences,Perm,Russia;2.Perm Regional Center for Protection against AIDS and Infectious Diseases,Perm,Russia;3.Institute of Immunology and Physiology, Ural Branch,Russian Academy of Sciences,Yekaterinburg,Russia;4.National Institute of Child Health and Human Development,Bethesda,USA;5.Case Western Reserve University,Cleveland,USA
Abstract:The level of proinflammatory markers was assessed in HIV-infected patients that were coinfected with hepatitis C virus (HCV) and had failed to restore the CD4+ T cell counts (immunological nonresponders, INR) during the antiretroviral therapy (ART). Among four patient groups (HIV+HCV and HIV+HCV+ subjects with the concordant response to ART; HIV+HCV and HIV+HCV+ subjects that were INR), the greatest systemic inflammation was in the latter group. The maximum difference was between the subjects HIV+HCVINR and HIV+HCV+ INR: the blood of coinfected patients contained significantly higher concentrations of the IP-10, sCD163, sTNF-RI, and sTNF-RII and of bacterial lipopolysaccharide. Systemic inflammation in HIV/HCV coinfected patients with the discordant response to ART is probably caused by a breach of hepatic barrier for the intestine products.
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