Kinetic host defense of the mice infected with Aspergillus Fumigatus

Future Microbiol. 2019 May:14:705-716. doi: 10.2217/fmb-2019-0043. Epub 2019 Jun 4.

Abstract

Aim:Aspergillus fumigatus is one of the most common opportunistic fungi that can cause invasive infection. To profile the kinetic variation of immune cells and cytokines after exposure to A. fumigatus thoroughly, we established a pulmonary A. fumigatus infection model in temporarily immunosuppressed mice. Materials & methods: Systematic and kinetic studies of different immune cells and cytokines were performed. Results: We observed that the granulocytes and macrophages recruited to the site of infection played an important role in the infectious phase. There was a significant increase in the cytokines IFN-γ, IL-6, TNF-α as well as the chemokines CXCL1, MIP-1α, MIP-2 and CCL5 after infection. IL-10 was found to participate in balancing the anti-inflammatory response in the recovery phases. The immune response mediated by T cells was mainly presented by the Th1-type on day 7 after exposure with a high proportion of IFN-γ+ CD4+ T cells and CD4+CD44highCD62Llow effector T cells. Conclusion: These kinetic parameters of the immune response might provide diagnostic clues for A. fumigatus infection.

Keywords: chemokines; cytokines; immune response.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Aspergillosis / immunology*
  • Aspergillus fumigatus / pathogenicity*
  • CD4-Positive T-Lymphocytes
  • Chemokine CCL3 / metabolism
  • Chemokine CCL5 / metabolism
  • Chemokine CXCL1 / metabolism
  • Chemokine CXCL2 / metabolism
  • Chemokines / blood
  • Chemokines / metabolism*
  • Cytokines / blood
  • Cytokines / metabolism*
  • Disease Models, Animal
  • Host-Pathogen Interactions / immunology*
  • Immunocompromised Host
  • Interferon-gamma / metabolism
  • Interleukin-10 / metabolism
  • Interleukin-6 / metabolism
  • Kinetics
  • Lung / microbiology
  • Lung / pathology
  • Lymph Nodes / microbiology
  • Lymph Nodes / pathology
  • Macrophages / immunology
  • Male
  • Mice
  • Mice, Inbred C57BL
  • Neutrophils / immunology
  • T-Lymphocytes / immunology
  • Th1 Cells / immunology
  • Tumor Necrosis Factor-alpha / metabolism

Substances

  • Ccl3 protein, mouse
  • Ccl5 protein, mouse
  • Chemokine CCL3
  • Chemokine CCL5
  • Chemokine CXCL1
  • Chemokine CXCL2
  • Chemokines
  • Cxcl1 protein, mouse
  • Cxcl2 protein, mouse
  • Cytokines
  • Interleukin-6
  • Tumor Necrosis Factor-alpha
  • Interleukin-10
  • Interferon-gamma