Surfactant protein A limits Pneumocystis murina infection in immunosuppressed C3H/HeN mice and modulates host response during infection

Microbes Infect. 2005 Apr;7(4):748-59. doi: 10.1016/j.micinf.2005.01.011. Epub 2005 Mar 22.

Abstract

The development of Pneumocystis murina pneumonia and host response were characterized over time and at different levels of infection in corticosteroid immunosuppressed surfactant protein A (SP-A) knockout and wild-type (WT) mice. Infection increased over time in both strains of mice; however, significantly more cyst forms were detected in the knockout mice at intermediate and late stages of infection. In mice with heavy infections, TNF-alpha and IFN-gamma protein concentrations were significantly higher in pulmonary lavage fluid from knockout mice. There was a significant positive correlation between TNF-alpha and IFN-gamma concentrations and the level of infection in knockout mice, but not in WT mice. No significant differences were detected in IL-1 levels between the two strains of mice at any of the time points or at any level of infection. At heavier infection levels, significantly more MIP-2 protein was detected in the lungs of knockout mice, but a significant positive correlation between MIP-2 concentrations and the infection level was detected in both groups of mice. At the intermediate stage of infection, a significantly higher percentage of neutrophils was detected in the lungs of knockout mice than in WT mice. There was no difference in SP-D levels between WT and KO mice with identical levels of infection. These data support a protective role for SP-A in host defense against Pneumocystis and suggest that the effects of SP-A on the host response vary based on the intensity of the infection.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, U.S. Gov't, Non-P.H.S.
  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Adrenal Cortex Hormones / pharmacology
  • Animals
  • Cytokines / metabolism
  • Immunosuppression Therapy
  • Inflammation / immunology
  • Inflammation / microbiology
  • Lung / immunology
  • Lung / microbiology
  • Mice
  • Mice, Knockout
  • Pneumocystis / isolation & purification
  • Pneumocystis / pathogenicity*
  • Pneumonia, Pneumocystis / immunology*
  • Pneumonia, Pneumocystis / microbiology
  • Pneumonia, Pneumocystis / physiopathology*
  • Pulmonary Surfactant-Associated Protein A / genetics
  • Pulmonary Surfactant-Associated Protein A / metabolism*

Substances

  • Adrenal Cortex Hormones
  • Cytokines
  • Pulmonary Surfactant-Associated Protein A