Animal models are used for the evaluation of the safety and immunogenicity of acellular pertussis vaccines before administration to humans. The aerosol challenge model provides a reproducible system for the study of virulence factors and immunity involved in respiratory infection and subsequent disease. Clinical studies have shown that acellular pertussis antigens are protective against disease; however, to date, there is no laboratory correlate of vaccine-mediated protection. In some recent publications, authors have suggested that when mice were immunized with DTP vaccines [with either whole-cell or acellular pertussis component] and then challenged with an aerosol or intranasal B. pertussis, the clearance of infection from the lungs paralleled the ability of these vaccines to protect children against pertussis. In previous studies in our laboratory, this aerosol model, despite very good intra- and inter-assay reproducibility, was not able to distinguish between with vaccines of high and low clinical efficacy. FY2002 activities: In FY 2002, our laboratory participated in an ongoing international, multi-center collaborative study that evaluated a model of murine intranasal infection for the assay of vaccines containing an acellular pertussis component. In the current study, participating laboratories evaluated vaccines of varying potency using the intranasal infection model. A draft report was reviewed and a WHO-sponsored meeting to discuss results and further studies is pending.

Agency
National Institute of Health (NIH)
Institute
Center for Biologics Evaluation and Research - Bactrial Products (CBERBP)
Type
Intramural Research (Z01)
Project #
1Z01BJ007003-19
Application #
6678405
Study Section
(LMDQ)
Project Start
Project End
Budget Start
Budget End
Support Year
19
Fiscal Year
2002
Total Cost
Indirect Cost