Resistance of MBL gene-knockout mice to experimental systemic aspergillosis

Karl V Clemons1, Marife Martinez, Ann-Jay Tong

  • 1California Institute for Medical Research, 2260 Clove Dr, San Jose, CA 95128, United States. clemons@cimr.org

Immunology Letters
|January 13, 2010
PubMed

Insights

Mannose-binding lectin (MBL) may harm rather than help during systemic aspergillosis. Studies in MBL-deficient mice suggest MBL might play a detrimental role in fighting Aspergillus fumigatus infections.

Area of Science:

  • Immunology
  • Infectious Diseases
  • Microbiology

Background:

  • Mannose-binding lectin (MBL) is a key component of the innate immune system.
  • MBL is believed to be important in combating invasive pulmonary aspergillosis.

Purpose of the Study:

  • To investigate the role of MBL in experimental systemic aspergillosis.
  • To determine if MBL deficiency impacts susceptibility to Aspergillus fumigatus infection.

Main Methods:

  • Utilized MBL-sufficient (WT) and MBL A and C gene-knockout (KO) mice.
  • Infected mice intravenously with varying inocula of Aspergillus fumigatus conidia.
  • Monitored survival rates and susceptibility to infection.

Main Results:

  • Both WT and KO mice exhibited dose-dependent susceptibility to infection.
  • KO mice were not more susceptible than WT mice in any experimental group.
  • At a reduced inoculum, KO mice showed significantly less susceptibility to lethal infection compared to WT mice.

Conclusions:

  • MBL may play a detrimental role in systemic aspergillosis.
  • These findings challenge the presumed protective role of MBL in Aspergillus infections.
  • Further research is needed to elucidate the complex role of MBL in fungal immunity.

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