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Infection and Immunity, November 2004, p. 6211-6220, Vol. 72, No. 11
0019-9567/04/$08.00+0     DOI: 10.1128/IAI.72.11.6211-6220.2004
Copyright © 2004, American Society for Microbiology. All Rights Reserved.

Passive Immunization of Neonatal Mice against Pneumocystis carinii f. sp. muris Enhances Control of Infection without Stimulating Inflammation

Kerry M. Empey,1 Melissa Hollifield,1 Kevin Schuer,1 Francis Gigliotti,2 and Beth A. Garvy1*

Departments of Microbiology, Immunology, and Molecular Genetics, Pharmaceutical Sciences, and Internal Medicine, University of Kentucky Medical Center, Lexington, Kentucky,1 Department of Pediatrics, University of Rochester, Rochester, New York2

Received 30 April 2004/ Returned for modification 19 May 2004/ Accepted 16 July 2004

Pneumocystis carinii is an opportunistic fungal pathogen that causes life-threatening pneumonia in immunocompromised individuals. Infants appear to be particularly susceptible to infection with Pneumocystis. We have previously shown that there is a significant delay in clearance of the organisms from the lungs of neonatal mice compared to adults. Since alveolar macrophages are the effector cells responsible for killing and clearance of Pneumocystis, we have examined alveolar macrophage activity in neonatal mice. We found that alveolar macrophage activation is delayed about 1 week in Pneumocystis-infected neonates compared to adults. Opsonization of the organism by Pneumocystis-specific antibody resulted in increased clearance of the organism in neonatal mice; however, there was decreased expression of activation markers on neonatal alveolar macrophages and reduced levels of cytokines associated with macrophage activation. Mice born to immunized dams had significant amounts of Pneumocystis-specific immunoglobulin G in their lungs and serum at day 7 postinfection, whereas mice born to naïve dams had merely detectable levels. This difference correlated with enhanced Pneumocystis clearance in mice born to immunized dams. The increase in specific antibody, however, did not result in significant inflammation in the lungs, as no differences in numbers of activated CD4+ cells were observed. Furthermore, there was no difference in cytokine or chemokine concentrations in the lungs of pups born to immune compared to naïve dams. These findings indicate that specific antibody plays an important role in Pneumocystis clearance from lungs of infected neonates; moreover, this process occurs without inducing inflammation in the lungs.


* Corresponding author. Mailing address: Department of Microbiology, Immunology, and Molecular Genetics, UKMC, Rm. MN668, 800 Rose St., Lexington, KY 40536-0298. Phone: (859) 323-5043. Fax: (859) 257-8994. E-mail: bgarv0{at}uky.edu.

Editor: T. R. Kozel


Infection and Immunity, November 2004, p. 6211-6220, Vol. 72, No. 11
0019-9567/04/$08.00+0     DOI: 10.1128/IAI.72.11.6211-6220.2004
Copyright © 2004, American Society for Microbiology. All Rights Reserved.




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