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Abstracts (complete list) - Wissenschaft Online

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Susanne Tartz, Holger Ruessmann, Jana Kamanova, Peter Sebo, Angelika Sturm, Volker<br />

Heussler, Bernhard Fleischer, Thomas Jacobs<br />

A heterologous prime/boost immunization using recombinant<br />

Salmonella and Bordetella adenylate cyclase induces<br />

<strong>complete</strong> protection against P. berghei malaria<br />

Sterile immunity against malaria can be achieved by the induction of cytokine-producing<br />

CD8+ T cells that target infected hepatocytes presenting epitopes of the<br />

circumsporozoite protein (CSP). In the present study we evaluate the protective efficacy<br />

of a heterologous prime/boost immunization protocol based on the delivery of the CD8+<br />

epitope of Plasmodium berghei CSP into the MHC class I presentation pathway, by<br />

either a type III secretion system of live recombinant Salmonella and/or by direct<br />

translocation of a recombinant Bordetella adenylate cyclase toxoid fusion (ACT-CSP)<br />

into the cytosol of CD11b-expressing professional antigen-presenting cells (APC). A<br />

single intraperitoneal application of the recombinant ACT-CSP toxoid, as well as a single<br />

oral immunization with the Salmonella vaccine, induced a specific CD8+ T cell response<br />

and the latter could be further enhanced by repeated application of the live vaccine,<br />

which however conferred only a partial protection on mice against a subsequent<br />

sporozoite challenge. In contrast, a heterologous prime/boost vaccination with the live<br />

Salmonella followed by ACT-CSP led to a significant enhancement of the CSP-specific T<br />

cell response and induced <strong>complete</strong> protection in all vaccinated mice

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