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Abstracts (complete list) - Wissenschaft Online

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Filiz Demircik, Ari Waisman<br />

The role of B cells and other antigen presenting cells in<br />

infections<br />

To clarify the role of B cells in infection models like Leishmania major, murine<br />

Cytomegalovirus (MCMV) and influenza, we are using three different mouse strains. The<br />

JHT mice are B cells deficient; the IgG1i strain has B cells producing and secreting IgG1<br />

antibodies but no other antibody isotypes; and the IgMi mice, which can produce IgM as<br />

the B cell receptor but have no antibodies in the sera. In these mouse strains we are<br />

looking for differences in the T cell repertoire that is established upon infection.<br />

Furthermore we want to deplete B cells and thereby look at their role in infection. To<br />

deplete B cells at distinct time points during, before or after clearing of the infection, we<br />

will establish a CD19-Cre x iDTR mouse. In this developed novel iDTR system, the<br />

diphtheria toxin receptor (DTR) can be expressed on the surface of cells following a Cremediated<br />

deletion of a STOP cassette. In the iDTR mice, lineage ablation is achieved by<br />

injecting diphtheria toxin (DT) into mice expressing the iDTR as well as a tissue specific<br />

Cre transgene. Finally we plan to create a new mouse with the DTR downstream of the<br />

CD11b promoter and then together with lineage specific Cre mouse strains we will be<br />

able to achieve a more specific ablation, especially for antigen presenting cells and be<br />

able, for example, to specifically delete cells that express CD11b and CD11c or CD11b<br />

and LysM. This system will allow us to specifically ablate sub-populations of dendritic<br />

cells, macrophages or B cells (B-1 cells) and study their role in different infectious<br />

systems.

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