Neutrophils from patients with advanced human immunodeficiency virus infection have impaired complement receptor function and preserved Fcgamma receptor function

J Infect Dis. 1999 Nov;180(5):1542-9. doi: 10.1086/315099.

Abstract

Interleukin (IL)-8 production by human polymorphonuclear leukocytes (PMNL) to Cryptococcus neoformans is related to complement activation. Generation of the bioactive fragments C3a and C5a is responsible for IL-8 release. IL-8 production was analyzed in response to C. neoformans by PMNL from persons with early- and late-stage (>400 and <200 CD4 cells/mm3, respectively) human immunodeficiency virus (HIV) infection who were at high risk for cryptococcosis. IL-8 release by PMNL from persons with early-stage infection and from healthy donors was similar; however, PMNL from persons with late-stage HIV infection had significantly impaired IL-8 production, which correlated with reduced IL-8 response to C3a and C5a proteins and decreased CD88 expression. Addition of murine monoclonal antibody (MAb) 18B7 promoted phagocytosis and restored IL-8 release consistent with integrity of FcgammaRIII. These results provide evidence for a selective defect in CD88 expression on PMNL from persons with late-stage HIV infection. However, Fcgamma receptor expression in PMNL appears to be intact and allows MAb to glucuronoxylomannan to positively influence PMNL function.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • Antibodies, Monoclonal / immunology
  • Candida albicans / immunology
  • Complement C3a / immunology
  • Complement C5a / immunology
  • Cryptococcus neoformans / immunology*
  • Flow Cytometry
  • HIV Infections / immunology*
  • Humans
  • Interleukin-8 / biosynthesis*
  • Neutrophils / immunology*
  • Receptors, Complement / metabolism*
  • Receptors, IgG / metabolism*

Substances

  • Antibodies, Monoclonal
  • Interleukin-8
  • Receptors, Complement
  • Receptors, IgG
  • Complement C3a
  • Complement C5a