Fcγ receptors and toll-like receptor 9 synergize to drive immune complex-induced dendritic cell maturation

Cell Immunol. 2019 Nov:345:103962. doi: 10.1016/j.cellimm.2019.103962. Epub 2019 Aug 3.

Abstract

Previous in vivo studies established that inactivated Francisella tularensis immune complexes (mAb-iFt) are a more protective vaccine against lethal tularemia than iFt alone. Subsequent in vitro studies revealed enhanced DC maturation marker expression with mAb-iFt stimulation. The goal of this study was to determine the mechanism of enhanced DC maturation. Multiparameter analysis of surface marker expression and cytokine secretion demonstrates a requirement for FcγR signaling in enhanced DC maturation. MyD88 was also found to be essential for heightened DC maturation, implicating MyD88-dependent TLRs in DC maturation. Upon further study, we discovered that TLRs 2 & 4 drive cytokine secretion, but surprisingly TLR9 is required for DC maturation marker upregulation. These studies reveal a separation of DC cytokine and maturation marker induction pathways and demonstrate that FcγR-TLR/MyD88 synergy underlies the enhanced dendritic cell maturation in response to the mAb-iFt vaccine.

Keywords: Dendritic cell maturation; Fcγ receptors; Flow cytometry; Francisella tularensis; Immune complex; MyD88; TLR2; TLR9.

Publication types

  • Research Support, N.I.H., Extramural

MeSH terms

  • Animals
  • Antibodies, Monoclonal / immunology
  • Bacterial Vaccines / immunology
  • Cell Differentiation / immunology*
  • Cytokines / immunology
  • Cytokines / metabolism
  • Dendritic Cells / immunology*
  • Dendritic Cells / metabolism
  • Francisella tularensis / immunology
  • Humans
  • Mice, Inbred C57BL
  • Mice, Knockout
  • Mice, Transgenic
  • Myeloid Differentiation Factor 88 / immunology*
  • Myeloid Differentiation Factor 88 / metabolism
  • Receptors, IgG / genetics
  • Receptors, IgG / immunology*
  • Toll-Like Receptor 2 / genetics
  • Toll-Like Receptor 2 / immunology
  • Toll-Like Receptor 2 / metabolism
  • Toll-Like Receptor 4 / genetics
  • Toll-Like Receptor 4 / immunology
  • Toll-Like Receptor 4 / metabolism
  • Toll-Like Receptor 9 / genetics
  • Toll-Like Receptor 9 / immunology*
  • Toll-Like Receptor 9 / metabolism
  • Tularemia / immunology
  • Tularemia / microbiology

Substances

  • Antibodies, Monoclonal
  • Bacterial Vaccines
  • Cytokines
  • FCGR1A protein, human
  • Myeloid Differentiation Factor 88
  • Receptors, IgG
  • Toll-Like Receptor 2
  • Toll-Like Receptor 4
  • Toll-Like Receptor 9