Antibody-Independent, CD4 + T-Cell-Dependent Protection against Pneumococcal Colonization Elicited by Intranasal Immunization with Purified Pneumococcal Proteins

Author:

Basset Alan1,Thompson Claudette M.2,Hollingshead Susan K.3,Briles David E.3,Ades Edwin W.4,Lipsitch Marc2,Malley Richard1

Affiliation:

1. Division of Infectious Diseases, Department of Medicine, Children's Hospital Boston, Boston, Massachusetts

2. Departments of Epidemiology, Immunology, and Infectious Diseases, Harvard School of Public Health, Boston, Massachusetts

3. Department of Microbiology, University of Alabama at Birmingham, Birmingham, Alabama

4. Division of Bacterial Diseases, National Center for Immunizations and Respiratory Diseases, Centers for Disease Control and Prevention, Atlanta, Georgia

Abstract

ABSTRACT Immunity to pneumococcal colonization in mice by exposure to live or killed pneumococci has been shown to be antibody independent but dependent on CD4 + T cells. Here we show that intranasal immunization with pneumococcal proteins (pneumococcal surface protein C, adhesin A, and a pneumolysoid) can elicit a similar mechanism of protection. Colonization could be significantly reduced in mice congenitally deficient in immunoglobulins after intranasal immunization with this mixture of proteins; conversely, the depletion of CD4 + T cells in immunized wild-type mice at the time of challenge eliminated the protection afforded by immunization. Overall, our results show that intranasal immunization with a mixture of pneumococcal proteins protects against colonization in an antibody-independent, CD4 + T-cell-dependent manner.

Publisher

American Society for Microbiology

Subject

Infectious Diseases,Immunology,Microbiology,Parasitology

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