Granulocyte-macrophage colony-stimulating factor (GM-CSF) restores allostimulatory function to accessory cells in patients with AIDS

HIV Clin Trials. 2002 May-Jun;3(3):219-24. doi: 10.1310/HP8B-NF27-VFWA-80YX.

Abstract

Background: Impaired allostimulatory function of dendritic cells in patients with AIDS has been reported previously. Granulocyte-macrophage colony-stimulating factor (GM-CSF) can restore the T-cell stimulatory function in transforming growth factor-beta 1 (TGF-beta 1)-inhibited murine accessory cells. We now report the effect of intravenous recombinant human GM-CSF (rhGM-CSF) on accessory cells of HIV-infected patients.

Method: The in vivo effect of GM-CSF on allostimulatory function of accessory cells was evaluated. Seventeen individuals with AIDS received a single infusion of rhGM-CSF (125 mg/m(2) over 120 minutes). Samples of peripheral blood lymphocytes (PBL) were taken at 1, 5, and 24 hours after infusion, and the allostimulatory capacity was measured.

Results: A single bolus infusion of rhGM-CSF resulted in significantly increased accessory cell function in 13/17 (88%) patients at one or more assayed time points after infusion.

Conclusion: These results suggest that the administration of rhGM-CSF can potentially restore allostimulatory function to accessory cells in HIV-infected patients, and this presents a novel way of immune reconstitution. Clinical significance of this approach of immune reconstitution in AIDS patients warrants further investigations.

Publication types

  • Clinical Trial

MeSH terms

  • AIDS Dementia Complex / drug therapy*
  • Adult
  • Dendritic Cells / immunology
  • Female
  • Granulocyte-Macrophage Colony-Stimulating Factor / administration & dosage
  • Granulocyte-Macrophage Colony-Stimulating Factor / pharmacology
  • Granulocyte-Macrophage Colony-Stimulating Factor / therapeutic use*
  • Humans
  • Immune Tolerance
  • Infusions, Intravenous
  • Lymphocyte Count
  • Male
  • Middle Aged
  • Pilot Projects
  • Receptors, Transforming Growth Factor beta / immunology
  • Recombinant Proteins
  • Treatment Outcome

Substances

  • Receptors, Transforming Growth Factor beta
  • Recombinant Proteins
  • Granulocyte-Macrophage Colony-Stimulating Factor