Soluble immune complexes shift the TLR-induced cytokine production of distinct polarized human macrophage subsets towards IL-10

PLoS One. 2012;7(4):e35994. doi: 10.1371/journal.pone.0035994. Epub 2012 Apr 26.

Abstract

Background: Costimulation of murine macrophages with immune complexes (ICs) and TLR ligands leads to alternative activation. Studies on human myeloid cells, however, indicate that ICs induce an increased pro-inflammatory cytokine production. This study aimed to clarify the effect of ICs on the pro- versus anti-inflammatory profile of human polarized macrophages.

Materials and methods: Monocytes isolated from peripheral blood of healthy donors were polarized for four days with IFN-γ, IL-4, IL-10, GM-CSF, M-CSF, or LPS, in the presence or absence of heat aggregated gamma-globulins (HAGGs). Phenotypic polarization markers were measured by flow cytometry. Polarized macrophages were stimulated with HAGGs or immobilized IgG alone or in combination with TLR ligands. TNF, IL-6, IL-10, IL-12, and IL-23 were measured by Luminex and/or RT-qPCR.

Results: HAGGs did not modulate the phenotypic polarization and the cytokine production of macrophages. However, HAGGs significantly altered the TLR-induced cytokine production of all polarized macrophage subsets, with the exception of MΦ(IL-4). In particular, HAGGs consistently enhanced the TLR-induced IL-10 production in both classically and alternatively polarized macrophages (M1 and M2). The effect of HAGGs on TNF and IL-6 production was less pronounced and depended on the polarization status, while IL-23p19 and IL-12p35 expression was not affected. In contrast with HAGGs, immobilized IgG induced a strong upregulation of not only IL-10, but also TNF and IL-6.

Conclusion: HAGGs alone do not alter the phenotype and cytokine production of in vitro polarized human macrophages. In combination with TLR-ligands, however, HAGGs but not immobilized IgG shift the cytokine production of distinct macrophage subsets toward IL-10.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Antigen-Antibody Complex / pharmacology
  • Cells, Cultured
  • Cytokines / genetics
  • Cytokines / metabolism*
  • Humans
  • Immobilized Proteins / chemistry
  • Immobilized Proteins / pharmacology
  • Immunoglobulin G / chemistry
  • Immunoglobulin G / pharmacology
  • Interleukin-10 / genetics
  • Interleukin-10 / metabolism*
  • Interleukin-23 / metabolism
  • Ligands
  • Lipopolysaccharides / toxicity
  • Macrophages / drug effects
  • Macrophages / immunology
  • Macrophages / metabolism*
  • Phenotype
  • Temperature
  • Toll-Like Receptors / chemistry
  • Toll-Like Receptors / metabolism*
  • Up-Regulation
  • gamma-Globulins / pharmacology

Substances

  • Antigen-Antibody Complex
  • Cytokines
  • Immobilized Proteins
  • Immunoglobulin G
  • Interleukin-23
  • Ligands
  • Lipopolysaccharides
  • Toll-Like Receptors
  • gamma-Globulins
  • Interleukin-10