Immunoglobulin G Fc(gamma) receptor expression on polymorphonuclear cells in bronchoalveolar lavage fluid of HIV-infected and HIV-seronegative patients with bacterial pneumonia

Clin Chem Lab Med. 2004 Feb;42(2):192-7. doi: 10.1515/CCLM.2004.035.

Abstract

This study was designed to test the hypothesis that impaired neutrophil function might contribute to the development of bacterial pneumonia in patients with HIV-infection. Numbers of inflammatory cells and immunoglobulin G Fcgamma receptor (IgG FcgammaR) I, II, III levels were investigated in bronchoalveolar lavage (BAL) fluid of HIV-seronegative and HIV-infected patients with bacterial pneumonia. The 99 patients were classified into three groups: I: HIV-seronegative and pneumonia (n = 40); II: HIV-infected and pneumonia (n = 19); III: HIV-seronegative with other pulmonary diseases than pneumonia (n = 40). The results of groups I and II, II and III, and I and III were compared. The percentage of alveolar macrophages was significantly lower (group II vs. III: p = 0.005, group I vs. III: p = 0.001), that of neutrophils increased significantly in patients with pneumonia (group II vs. III: p = 0.02, group I vs. III: p = 0.01). Lymphocytes differed only between groups I and III (p = 0.04). Although only the expression of FcgammaRI was significantly higher in HIV-seronegative pneumonia patients compared to those without pneumonia (p = 0.01), the mean expression of all three receptors was lower in the HIV-infected group, with that of FcgammaRI approaching statistical significance. This report provides first evidence that altered FcgammaR expression on BAL neutrophils might contribute to the increased susceptibility of HIV-infected patients to bacterial pneumonia.

Publication types

  • Comparative Study

MeSH terms

  • Adult
  • Bronchoalveolar Lavage Fluid / immunology*
  • Female
  • Flow Cytometry
  • HIV Infections / immunology*
  • HIV Seronegativity / immunology*
  • Humans
  • Male
  • Middle Aged
  • Neutrophils / immunology*
  • Pneumonia, Bacterial / immunology*
  • Receptors, IgG / biosynthesis*
  • Receptors, IgG / immunology

Substances

  • Receptors, IgG