Reduced type 1 and type 2 cytokines in antiviral memory T helper function among women coinfected with HIV and HCV

J Clin Immunol. 2005 Mar;25(2):134-41. doi: 10.1007/s10875-005-2819-x.

Abstract

Bias in cytokine responses has been proposed as a contributing mechanism to pathogenesis in persistent HIV or hepatitis C virus (HCV) infections. We investigated whether coinfection with HCV modifies the profile of antigen-specific cytokine secretion in women persistently infected with HIV compared to women with single HIV or HCV infection. The T helper response to HIV, HCV and cytomegalovirus (CMV) as a positive viral control was dominated by type 1 cytokines (interleukin- [IL] 2, interferon- [IFN] gamma and tumor necrosis factor- [TNF] alpha), with IFN-gamma as the most abundantly secreted. IL-4, IL-5 and IL-10 were low in healthy controls and patients. Robust CMV-specific responses contrasted with curtailed HCV-specific responses in HCV-infected women. The overall anti-viral profile was dominated by Th1 cytokines even in coinfected women but both type 1 and type 2 responses were reduced in HIV-infected women and more extensively in women with HCV/HIV coinfection.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • CD4 Antigens / metabolism
  • Cells, Cultured
  • Cytokines / metabolism*
  • Female
  • HIV / physiology
  • HIV Infections / complications*
  • HIV Infections / immunology*
  • HIV Infections / metabolism
  • HIV Infections / virology
  • Hepacivirus / physiology
  • Hepatitis C / complications*
  • Hepatitis C / immunology*
  • Hepatitis C / metabolism
  • Hepatitis C / virology
  • Humans
  • Immunologic Memory / immunology*
  • Male
  • Middle Aged
  • T-Lymphocytes, Helper-Inducer / immunology*
  • T-Lymphocytes, Helper-Inducer / metabolism

Substances

  • CD4 Antigens
  • Cytokines