PTX3 binds MD-2 and promotes TRIF-dependent immune protection in aspergillosis

J Immunol. 2014 Sep 1;193(5):2340-8. doi: 10.4049/jimmunol.1400814. Epub 2014 Jul 21.

Abstract

The long pentraxin 3 (PTX3) modulates different effector pathways involved in innate resistance to Aspergillus fumigatus, including complement activation or promotion of phagocytosis by interacting with FcγRs. However, whether and how TLRs modulate PTX3 mediates antifungal resistance is not known. In this study, we demonstrate that PTX3 binds myeloid differentiation protein 2 (MD-2) in vitro and exerts its protective antifungal activity in vivo through TLR4/MD-2-mediated signaling. Similar to Tlr4(-/-) mice, Md2(-/-) mice displayed high susceptibility to pulmonary aspergillosis, a phenotype associated with a proinflammatory cytokine profile and impaired antifungal activity of polymorphonuclear neutrophils. Treating Md2(-/-) mice with PTX3 failed to confer immune protection against the fungus, whereas adoptive transfer of MD-2-competent polymorphonuclear neutrophils restored it. Mechanistically, engagement of MD-2 by PTX3-opsonized Aspergillus conidia activated the TLR4/Toll/IL-1R domain-containing adapter inducing IFN-β-dependent signaling pathway converging on IL-10. Thus, we have identified a novel receptor mechanism, involving the TLR4/MD-2/Toll/IL-1R domain-containing adapter inducing IFN-β-mediated signaling, whereby PTX3 elicits antifungal resistance with limited immunopathology in A. fumigatus infection.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adaptor Proteins, Vesicular Transport / genetics
  • Adaptor Proteins, Vesicular Transport / immunology*
  • Animals
  • Aspergillosis / genetics
  • Aspergillosis / immunology*
  • Aspergillosis / pathology
  • Aspergillus fumigatus / genetics
  • Aspergillus fumigatus / immunology*
  • C-Reactive Protein / genetics
  • C-Reactive Protein / immunology*
  • HEK293 Cells
  • Humans
  • Interferon-beta / genetics
  • Interferon-beta / immunology
  • Interleukin-10 / genetics
  • Interleukin-10 / immunology
  • Lymphocyte Antigen 96 / genetics
  • Lymphocyte Antigen 96 / immunology*
  • Mice
  • Mice, Inbred BALB C
  • Mice, Knockout
  • Nerve Tissue Proteins / genetics
  • Nerve Tissue Proteins / immunology*
  • Serum Amyloid P-Component / genetics
  • Serum Amyloid P-Component / immunology*
  • Signal Transduction / genetics
  • Signal Transduction / immunology
  • Toll-Like Receptor 4 / genetics
  • Toll-Like Receptor 4 / immunology

Substances

  • Adaptor Proteins, Vesicular Transport
  • IL10 protein, human
  • IL10 protein, mouse
  • LY96 protein, human
  • Ly96 protein, mouse
  • Lymphocyte Antigen 96
  • Nerve Tissue Proteins
  • Serum Amyloid P-Component
  • TICAM-1 protein, mouse
  • TICAM1 protein, human
  • TLR4 protein, human
  • Tlr4 protein, mouse
  • Toll-Like Receptor 4
  • neuronal pentraxin
  • Interleukin-10
  • PTX3 protein
  • Interferon-beta
  • C-Reactive Protein