Pathological examination of lung tissues in influenza a virus-infected mice

Nilton Akio Muto1, Yuji Sunden, Tomoe Hattori

  • 1Division of Molecular Pathobiology, Research Center for Zoonosis Control, Hokkaido University, Sapporo, Japan.

Insights

Aged mice infected with influenza virus exhibit delayed body weight loss and milder lung pathology compared to young mice. This is linked to lower immune cell infiltration, suggesting age-specific differences in viral infection response.

Area of Science:

  • Immunology
  • Pathology
  • Virology

Background:

  • Influenza virus infection impacts different age groups variably.
  • Understanding age-related differences in host response is crucial for managing viral infections.

Purpose of the Study:

  • To compare the pathological changes and immune responses in the lungs of young and aged mice infected with influenza virus.
  • To investigate the correlation between immune cell infiltration and disease progression in different age groups.

Main Methods:

  • Histopathological examination of lung tissues.
  • Immunohistochemical analysis to detect viral antigens and immune cell infiltration (T cells, macrophages, polymorphonuclear leukocytes - PMNs).
  • Monitoring of body weight changes post-infection.

Main Results:

  • Young mice showed earlier body weight loss and higher viral antigen-positive cells at 3 days post-infection (dpi) compared to aged mice.
  • Aged mice exhibited delayed onset of body weight loss (9 dpi) and prolonged presence of viral antigens.
  • Young mice displayed more severe bronchointerstitial pneumonia with significant infiltration of PMNs, T cells, and macrophages at 6-9 dpi, while aged mice showed milder pathology and lower immune cell accumulation.

Conclusions:

  • Aged mice demonstrate a delayed and less severe response to influenza virus infection, characterized by reduced immune cell infiltration.
  • Lower levels of PMNs, macrophages, and T lymphocytes in aged mice correlate with delayed weight loss and persistent infection.
  • These findings highlight significant age-specific differences in lung pathology and immune response during influenza virus infection.

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