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Priming of CD8+ T cells: regulation of proliferation and development into effector and/or memory cells

proteomics dataset

We obtained microarray and RT-PCR data on the priming of CD8+ T cells in mice and their regulation of proliferation and development into effector and/or memory cells.

The positive influence of a reactive lymph node on the priming of CD8+ T-cells was already analyzed in 2007. We set up experiments to determine if this effect would benefit a response against a second infection. We infected mice with CD8+ T-cells primed with or without the influence of a reactive lymph node with a flu-virus encoding the specific antigen. After several days we determined the viral load in the lungs with RT-PCR. The results show that in mice with CD8+ T-cells primed with a reactive lymph node the viral load in the lungs was significantly smaller then in a control mice.
We also determined that suboptimally primed CD8+ T-cells can develop into functional memory cells. Although suboptimally primed CD8+ T-cells do not display good effector function, as previously enclosed, we found that they were efficient at eradicating tumors in the memory phase.
Micro-array data obtained from samples from suboptimally primed CD8+ T-cells compared with optimally primed CD8+ T-cells showed several interesting genes involved in regulation of proliferation and development.

We are currently working on verifying the data obtained with micro-arrays through RT-PCR, and comparing data from in vitro primed CD8+ T-cells to in vivo primed CD8+ T-cells. We intend to analyse the candidate genes through overexpression and siRNA experiments.






created over 15 years ago (8 December 2009)    last modified over 12 years ago (5 November 2012)   [ RDF Rdf ]   [ RelFinder Relfinder ]