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* Queensland Institute of Medical Research and
CRC for Vaccine Technology, Brisbane, Australia; and
Australian Centre for International and Tropical Health and Nutrition, University of Queensland, Brisbane, Australia
Immunizing pregnant women with a malaria vaccine is one approach to protecting the mother and her offspring from malaria infection. However, specific maternal Abs generated in response to vaccination and transferred to the fetus may interfere with the infants ability to respond to the same vaccine. Using a murine model of malaria, we examined the effect of maternal 19-kDa C-terminal region of merozoite surface protein-1 (MSP119) and Plasmodium yoelii Abs on the pups ability to respond to immunization with MSP119. Maternal MSP119-specific Abs but not P. yoelii-specific Abs inhibited Ab production following MSP119 immunization in 2-wk-old pups. This inhibition was correlated with the amount of maternal MSP119 Ab present in the pup at the time of immunization and was due to fewer specific B cells. Passively acquired Ab most likely inhibited the development of an Ab response by blocking access to critical B cell epitopes. If a neonates ability to respond to MSP119 vaccination depends on the level of maternal Abs present at the time of vaccination, it may be necessary to delay immunization until Abs specific for the vaccinating Ag have decreased.
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